what is the purpose in drawing conclusions in research

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• > How to Do Research
• > Draw conclusions and make recommendations

Book contents

• Frontmatter
• Acknowledgements
• Introduction: Types of research
• Part 1 The research process
• 1 Develop the research objectives
• 2 Design and plan the study
• 3 Write the proposal
• 4 Obtain financial support for the research
• 5 Manage the research
• 6 Draw conclusions and make recommendations
• 7 Write the report
• 8 Disseminate the results
• Part 2 Methods
• Appendix The market for information professionals: A proposal from the Policy Studies Institute

6 - Draw conclusions and make recommendations

from Part 1 - The research process

Published online by Cambridge University Press:  09 June 2018

This is the point everything has been leading up to. Having carried out the research and marshalled all the evidence, you are now faced with the problem of making sense of it all. Here you need to distinguish clearly between three different things: results, conclusions and recommendations.

Results are what you have found through the research. They are more than just the raw data that you have collected. They are the processed findings of the work – what you have been analysing and striving to understand. In total, the results form the picture that you have uncovered through your research. Results are neutral. They clearly depend on the nature of the questions asked but, given a particular set of questions, the results should not be contentious – there should be no debate about whether or not 63 per cent of respondents said ‘yes’ to question 16.

When you consider the results you can draw conclusions based on them. These are less neutral as you are putting your interpretation on the results and thus introducing a degree of subjectivity. Some research is simply descriptive – the final report merely presents the results. In most cases, though, you will want to interpret them, saying what they mean for you – drawing conclusions.

These conclusions might arise from a comparison between your results and the findings of other studies. They will, almost certainly, be developed with reference to the aim and objectives of the research. While there will be no debate over the results, the conclusions could well be contentious. Someone else might interpret the results differently, arriving at different conclusions. For this reason you need to support your conclusions with structured, logical reasoning.

Having drawn your conclusions you can then make recommendations. These should flow from your conclusions. They are suggestions about action that might be taken by people or organizations in the light of the conclusions that you have drawn from the results of the research. Like the conclusions, the recommendations may be open to debate. You may feel that, on the basis of your conclusions, the organization you have been studying should do this, that or the other.

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• Draw conclusions and make recommendations
• Book: How to Do Research
• Online publication: 09 June 2018
• Chapter DOI: https://doi.org/10.29085/9781856049825.007

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• Research paper

Writing a Research Paper Conclusion | Step-by-Step Guide

Published on October 30, 2022 by Jack Caulfield . Revised on April 13, 2023.

• Restate the problem statement addressed in the paper
• Summarize your overall arguments or findings
• Suggest the key takeaways from your paper

The content of the conclusion varies depending on whether your paper presents the results of original empirical research or constructs an argument through engagement with sources .

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Table of contents

Step 1: restate the problem, step 2: sum up the paper, step 3: discuss the implications, research paper conclusion examples, frequently asked questions about research paper conclusions.

The first task of your conclusion is to remind the reader of your research problem . You will have discussed this problem in depth throughout the body, but now the point is to zoom back out from the details to the bigger picture.

While you are restating a problem you’ve already introduced, you should avoid phrasing it identically to how it appeared in the introduction . Ideally, you’ll find a novel way to circle back to the problem from the more detailed ideas discussed in the body.

For example, an argumentative paper advocating new measures to reduce the environmental impact of agriculture might restate its problem as follows:

Meanwhile, an empirical paper studying the relationship of Instagram use with body image issues might present its problem like this:

“In conclusion …”

Avoid starting your conclusion with phrases like “In conclusion” or “To conclude,” as this can come across as too obvious and make your writing seem unsophisticated. The content and placement of your conclusion should make its function clear without the need for additional signposting.

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Having zoomed back in on the problem, it’s time to summarize how the body of the paper went about addressing it, and what conclusions this approach led to.

Depending on the nature of your research paper, this might mean restating your thesis and arguments, or summarizing your overall findings.

Argumentative paper: Restate your thesis and arguments

In an argumentative paper, you will have presented a thesis statement in your introduction, expressing the overall claim your paper argues for. In the conclusion, you should restate the thesis and show how it has been developed through the body of the paper.

Briefly summarize the key arguments made in the body, showing how each of them contributes to proving your thesis. You may also mention any counterarguments you addressed, emphasizing why your thesis holds up against them, particularly if your argument is a controversial one.

Don’t go into the details of your evidence or present new ideas; focus on outlining in broad strokes the argument you have made.

Empirical paper: Summarize your findings

In an empirical paper, this is the time to summarize your key findings. Don’t go into great detail here (you will have presented your in-depth results and discussion already), but do clearly express the answers to the research questions you investigated.

Describe your main findings, even if they weren’t necessarily the ones you expected or hoped for, and explain the overall conclusion they led you to.

Having summed up your key arguments or findings, the conclusion ends by considering the broader implications of your research. This means expressing the key takeaways, practical or theoretical, from your paper—often in the form of a call for action or suggestions for future research.

Argumentative paper: Strong closing statement

An argumentative paper generally ends with a strong closing statement. In the case of a practical argument, make a call for action: What actions do you think should be taken by the people or organizations concerned in response to your argument?

If your topic is more theoretical and unsuitable for a call for action, your closing statement should express the significance of your argument—for example, in proposing a new understanding of a topic or laying the groundwork for future research.

Empirical paper: Future research directions

In a more empirical paper, you can close by either making recommendations for practice (for example, in clinical or policy papers), or suggesting directions for future research.

Whatever the scope of your own research, there will always be room for further investigation of related topics, and you’ll often discover new questions and problems during the research process .

Finish your paper on a forward-looking note by suggesting how you or other researchers might build on this topic in the future and address any limitations of the current paper.

Full examples of research paper conclusions are shown in the tabs below: one for an argumentative paper, the other for an empirical paper.

• Argumentative paper
• Empirical paper

While the role of cattle in climate change is by now common knowledge, countries like the Netherlands continually fail to confront this issue with the urgency it deserves. The evidence is clear: To create a truly futureproof agricultural sector, Dutch farmers must be incentivized to transition from livestock farming to sustainable vegetable farming. As well as dramatically lowering emissions, plant-based agriculture, if approached in the right way, can produce more food with less land, providing opportunities for nature regeneration areas that will themselves contribute to climate targets. Although this approach would have economic ramifications, from a long-term perspective, it would represent a significant step towards a more sustainable and resilient national economy. Transitioning to sustainable vegetable farming will make the Netherlands greener and healthier, setting an example for other European governments. Farmers, policymakers, and consumers must focus on the future, not just on their own short-term interests, and work to implement this transition now.

As social media becomes increasingly central to young people’s everyday lives, it is important to understand how different platforms affect their developing self-conception. By testing the effect of daily Instagram use among teenage girls, this study established that highly visual social media does indeed have a significant effect on body image concerns, with a strong correlation between the amount of time spent on the platform and participants’ self-reported dissatisfaction with their appearance. However, the strength of this effect was moderated by pre-test self-esteem ratings: Participants with higher self-esteem were less likely to experience an increase in body image concerns after using Instagram. This suggests that, while Instagram does impact body image, it is also important to consider the wider social and psychological context in which this usage occurs: Teenagers who are already predisposed to self-esteem issues may be at greater risk of experiencing negative effects. Future research into Instagram and other highly visual social media should focus on establishing a clearer picture of how self-esteem and related constructs influence young people’s experiences of these platforms. Furthermore, while this experiment measured Instagram usage in terms of time spent on the platform, observational studies are required to gain more insight into different patterns of usage—to investigate, for instance, whether active posting is associated with different effects than passive consumption of social media content.

If you’re unsure about the conclusion, it can be helpful to ask a friend or fellow student to read your conclusion and summarize the main takeaways.

• Do they understand from your conclusion what your research was about?
• Are they able to summarize the implications of your findings?
• Can they answer your research question based on your conclusion?

You can also get an expert to proofread and feedback your paper with a paper editing service .

The conclusion of a research paper has several key elements you should make sure to include:

• A restatement of the research problem
• A summary of your key arguments and/or findings
• A short discussion of the implications of your research

No, it’s not appropriate to present new arguments or evidence in the conclusion . While you might be tempted to save a striking argument for last, research papers follow a more formal structure than this.

All your findings and arguments should be presented in the body of the text (more specifically in the results and discussion sections if you are following a scientific structure). The conclusion is meant to summarize and reflect on the evidence and arguments you have already presented, not introduce new ones.

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Online Guide to Writing and Research

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• Online Guide to Writing

Planning and Writing a Research Paper

Draw Conclusions

As a writer, you are presenting your viewpoint, opinions, evidence, etc. for others to review, so you must take on this task with maturity, courage and thoughtfulness.  Remember, you are adding to the discourse community with every research paper that you write.  This is a privilege and an opportunity to share your point of view with the world at large in an academic setting.

Because research generates further research, the conclusions you draw from your research are important. As a researcher, you depend on the integrity of the research that precedes your own efforts, and researchers depend on each other to draw valid conclusions. 

To test the validity of your conclusions, you will have to review both the content of your paper and the way in which you arrived at the content. You may ask yourself questions, such as the ones presented below, to detect any weak areas in your paper, so you can then make those areas stronger.  Notice that some of the questions relate to your process, others to your sources, and others to how you arrived at your conclusions.

Checklist for Evaluating Your Conclusions

Key Takeaways

• Because research generates further research, the conclusions you draw from your research are important.
• To test the validity of your conclusions, you will have to review both the content of your paper and the way in which you arrived at the content.

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Table of Contents: Online Guide to Writing

Chapter 1: College Writing

How Does College Writing Differ from Workplace Writing?

What Is College Writing?

Why So Much Emphasis on Writing?

Chapter 2: The Writing Process

Doing Exploratory Research

Getting from Notes to Your Draft

Introduction

Prewriting - Techniques to Get Started - Mining Your Intuition

Prewriting: Targeting Your Audience

Prewriting: Techniques to Get Started

Prewriting: Understanding Your Assignment

Rewriting: Being Your Own Critic

Rewriting: Creating a Revision Strategy

Rewriting: Getting Feedback

Rewriting: The Final Draft

Techniques to Get Started - Outlining

Techniques to Get Started - Using Systematic Techniques

Thesis Statement and Controlling Idea

Writing: Getting from Notes to Your Draft - Freewriting

Writing: Getting from Notes to Your Draft - Summarizing Your Ideas

Writing: Outlining What You Will Write

Chapter 3: Thinking Strategies

A Word About Style, Voice, and Tone

A Word About Style, Voice, and Tone: Style Through Vocabulary and Diction

Critical Strategies and Writing

Critical Strategies and Writing: Analysis

Critical Strategies and Writing: Evaluation

Critical Strategies and Writing: Persuasion

Critical Strategies and Writing: Synthesis

Developing a Paper Using Strategies

Kinds of Assignments You Will Write

Patterns for Presenting Information

Patterns for Presenting Information: Critiques

Patterns for Presenting Information: Discussing Raw Data

Patterns for Presenting Information: General-to-Specific Pattern

Patterns for Presenting Information: Problem-Cause-Solution Pattern

Patterns for Presenting Information: Specific-to-General Pattern

Patterns for Presenting Information: Summaries and Abstracts

Supporting with Research and Examples

Writing Essay Examinations

Writing Essay Examinations: Make Your Answer Relevant and Complete

Writing Essay Examinations: Organize Thinking Before Writing

Writing Essay Examinations: Read and Understand the Question

Chapter 4: The Research Process

Planning and Writing a Research Paper: Ask a Research Question

Planning and Writing a Research Paper: Cite Sources

Planning and Writing a Research Paper: Collect Evidence

Planning and Writing a Research Paper: Decide Your Point of View, or Role, for Your Research

Planning and Writing a Research Paper: Draw Conclusions

Planning and Writing a Research Paper: Find a Topic and Get an Overview

Planning and Writing a Research Paper: Manage Your Resources

Planning and Writing a Research Paper: Outline

Planning and Writing a Research Paper: Survey the Literature

Planning and Writing a Research Paper: Work Your Sources into Your Research Writing

Research Resources: Where Are Research Resources Found? - Human Resources

Research Resources: What Are Research Resources?

Research Resources: Where Are Research Resources Found?

Research Resources: Where Are Research Resources Found? - Electronic Resources

Research Resources: Where Are Research Resources Found? - Print Resources

Structuring the Research Paper: Formal Research Structure

Structuring the Research Paper: Informal Research Structure

The Nature of Research

The Research Assignment: How Should Research Sources Be Evaluated?

The Research Assignment: When Is Research Needed?

The Research Assignment: Why Perform Research?

Chapter 5: Academic Integrity

Academic Integrity

Giving Credit to Sources

Giving Credit to Sources: Copyright Laws

Giving Credit to Sources: Documentation

Giving Credit to Sources: Style Guides

Integrating Sources

Practicing Academic Integrity

Practicing Academic Integrity: Keeping Accurate Records

Practicing Academic Integrity: Managing Source Material

Practicing Academic Integrity: Managing Source Material - Paraphrasing Your Source

Practicing Academic Integrity: Managing Source Material - Quoting Your Source

Practicing Academic Integrity: Managing Source Material - Summarizing Your Sources

Types of Documentation

Types of Documentation: Bibliographies and Source Lists

Types of Documentation: Citing World Wide Web Sources

Types of Documentation: In-Text or Parenthetical Citations

Types of Documentation: In-Text or Parenthetical Citations - APA Style

Types of Documentation: In-Text or Parenthetical Citations - CSE/CBE Style

Types of Documentation: In-Text or Parenthetical Citations - Chicago Style

Types of Documentation: In-Text or Parenthetical Citations - MLA Style

Types of Documentation: Note Citations

Chapter 6: Using Library Resources

Finding Library Resources

Chapter 7: Assessing Your Writing

How Is Writing Graded?

How Is Writing Graded?: A General Assessment Tool

The Draft Stage

The Draft Stage: The First Draft

The Draft Stage: The Revision Process and the Final Draft

The Draft Stage: Using Feedback

The Research Stage

Using Assessment to Improve Your Writing

Chapter 8: Other Frequently Assigned Papers

Reviews and Reaction Papers: Article and Book Reviews

Reviews and Reaction Papers: Reaction Papers

Writing Arguments

Writing Arguments: Adapting the Argument Structure

Writing Arguments: Purposes of Argument

Writing Arguments: References to Consult for Writing Arguments

Writing Arguments: Steps to Writing an Argument - Anticipate Active Opposition

Writing Arguments: Steps to Writing an Argument - Determine Your Organization

Writing Arguments: Steps to Writing an Argument - Develop Your Argument

Writing Arguments: Steps to Writing an Argument - Introduce Your Argument

Writing Arguments: Steps to Writing an Argument - State Your Thesis or Proposition

Writing Arguments: Steps to Writing an Argument - Write Your Conclusion

Writing Arguments: Types of Argument

Appendix A: Books to Help Improve Your Writing

Dictionaries

General Style Manuals

Researching on the Internet

Special Style Manuals

Writing Handbooks

Appendix B: Collaborative Writing and Peer Reviewing

Collaborative Writing: Assignments to Accompany the Group Project

Collaborative Writing: Informal Progress Report

Collaborative Writing: Issues to Resolve

Collaborative Writing: Methodology

Collaborative Writing: Peer Evaluation

Collaborative Writing: Tasks of Collaborative Writing Group Members

Collaborative Writing: Writing Plan

General Introduction

Peer Reviewing

Appendix C: Developing an Improvement Plan

Working with Your Instructor’s Comments and Grades

Appendix D: Writing Plan and Project Schedule

Devising a Writing Project Plan and Schedule

Reviewing Your Plan with Others

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Drawing Conclusions and Reporting the Results

Rajiv S. Jhangiani; I-Chant A. Chiang; Carrie Cuttler; and Dana C. Leighton

Learning Objectives

• Identify the conclusions researchers can make based on the outcome of their studies.
• Describe why scientists avoid the term “scientific proof.”
• Explain the different ways that scientists share their findings.

Drawing Conclusions

Since statistics are probabilistic in nature and findings can reflect type I or type II errors, we cannot use the results of a single study to conclude with certainty that a theory is true. Rather theories are supported, refuted, or modified based on the results of research.

If the results are statistically significant and consistent with the hypothesis and the theory that was used to generate the hypothesis, then researchers can conclude that the theory is supported. Not only did the theory make an accurate prediction, but there is now a new phenomenon that the theory accounts for. If a hypothesis is disconfirmed in a systematic empirical study, then the theory has been weakened. It made an inaccurate prediction, and there is now a new phenomenon that it does not account for.

Although this seems straightforward, there are some complications. First, confirming a hypothesis can strengthen a theory but it can never prove a theory. In fact, scientists tend to avoid the word “prove” when talking and writing about theories. One reason for this avoidance is that the result may reflect a type I error.  Another reason for this  avoidance  is that there may be other plausible theories that imply the same hypothesis, which means that confirming the hypothesis strengthens all those theories equally. A third reason is that it is always possible that another test of the hypothesis or a test of a new hypothesis derived from the theory will be disconfirmed. This  difficulty  is a version of the famous philosophical “problem of induction.” One cannot definitively prove a general principle (e.g., “All swans are white.”) just by observing confirming cases (e.g., white swans)—no matter how many. It is always possible that a disconfirming case (e.g., a black swan) will eventually come along. For these reasons, scientists tend to think of theories—even highly successful ones—as subject to revision based on new and unexpected observations.

A second complication has to do with what it means when a hypothesis is disconfirmed. According to the strictest version of the hypothetico-deductive method, disconfirming a hypothesis disproves the theory it was derived from. In formal logic, the premises “if  A  then  B ” and “not  B ” necessarily lead to the conclusion “not  A .” If  A  is the theory and  B  is the hypothesis (“if  A  then  B ”), then disconfirming the hypothesis (“not  B ”) must mean that the theory is incorrect (“not  A ”). In practice, however, scientists do not give up on their theories so easily. One reason is that one disconfirmed hypothesis could be a missed opportunity (the result of a type II error) or it could be the result of a faulty research design. Perhaps the researcher did not successfully manipulate the independent variable or measure the dependent variable.

A disconfirmed hypothesis could also mean that some unstated but relatively minor assumption of the theory was not met. For example, if Zajonc had failed to find social facilitation in cockroaches, he could have concluded that drive theory is still correct but it applies only to animals with sufficiently complex nervous systems. That is, the evidence from a study can be used to modify a theory.  This practice does not mean that researchers are free to ignore disconfirmations of their theories. If they cannot improve their research designs or modify their theories to account for repeated disconfirmations, then they eventually must abandon their theories and replace them with ones that are more successful.

The bottom line here is that because statistics are probabilistic in nature and because all research studies have flaws there is no such thing as scientific proof, there is only scientific evidence.

Reporting the Results

The final step in the research process involves reporting the results. As described in the section on Reviewing the Research Literature in this chapter, results are typically reported in peer-reviewed journal articles and at conferences.

The most prestigious way to report one’s findings is by writing a manuscript and having it published in a peer-reviewed scientific journal. Manuscripts published in psychology journals typically must adhere to the writing style of the American Psychological Association (APA style). You will likely be learning the major elements of this writing style in this course.

Another way to report findings is by writing a book chapter that is published in an edited book. Preferably the editor of the book puts the chapter through peer review but this is not always the case and some scientists are invited by editors to write book chapters.

A fun way to disseminate findings is to give a presentation at a conference. This can either be done as an oral presentation or a poster presentation. Oral presentations involve getting up in front of an audience of fellow scientists and giving a talk that might last anywhere from 10 minutes to 1 hour (depending on the conference) and then fielding questions from the audience. Alternatively, poster presentations involve summarizing the study on a large poster that provides a brief overview of the purpose, methods, results, and discussion. The presenter stands by their poster for an hour or two and discusses it with people who pass by. Presenting one’s work at a conference is a great way to get feedback from one’s peers before attempting to undergo the more rigorous peer-review process involved in publishing a journal article.

Drawing Conclusions and Reporting the Results Copyright © by Rajiv S. Jhangiani; I-Chant A. Chiang; Carrie Cuttler; and Dana C. Leighton is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License , except where otherwise noted.

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How to Write a Conclusion for Research Papers (with Examples)

The conclusion of a research paper is a crucial section that plays a significant role in the overall impact and effectiveness of your research paper. However, this is also the section that typically receives less attention compared to the introduction and the body of the paper. The conclusion serves to provide a concise summary of the key findings, their significance, their implications, and a sense of closure to the study. Discussing how can the findings be applied in real-world scenarios or inform policy, practice, or decision-making is especially valuable to practitioners and policymakers. The research paper conclusion also provides researchers with clear insights and valuable information for their own work, which they can then build on and contribute to the advancement of knowledge in the field.

The research paper conclusion should explain the significance of your findings within the broader context of your field. It restates how your results contribute to the existing body of knowledge and whether they confirm or challenge existing theories or hypotheses. Also, by identifying unanswered questions or areas requiring further investigation, your awareness of the broader research landscape can be demonstrated.

Remember to tailor the research paper conclusion to the specific needs and interests of your intended audience, which may include researchers, practitioners, policymakers, or a combination of these.

Table of Contents

What is a conclusion in a research paper, summarizing conclusion, editorial conclusion, externalizing conclusion, importance of a good research paper conclusion, how to write a conclusion for your research paper, research paper conclusion examples.

• How to write a research paper conclusion with Paperpal? 

Frequently Asked Questions

A conclusion in a research paper is the final section where you summarize and wrap up your research, presenting the key findings and insights derived from your study. The research paper conclusion is not the place to introduce new information or data that was not discussed in the main body of the paper. When working on how to conclude a research paper, remember to stick to summarizing and interpreting existing content. The research paper conclusion serves the following purposes: 1

• Warn readers of the possible consequences of not attending to the problem.
• Recommend specific course(s) of action.
• Restate key ideas to drive home the ultimate point of your research paper.
• Provide a “take-home” message that you want the readers to remember about your study.

Types of conclusions for research papers

In research papers, the conclusion provides closure to the reader. The type of research paper conclusion you choose depends on the nature of your study, your goals, and your target audience. I provide you with three common types of conclusions:

A summarizing conclusion is the most common type of conclusion in research papers. It involves summarizing the main points, reiterating the research question, and restating the significance of the findings. This common type of research paper conclusion is used across different disciplines.

An editorial conclusion is less common but can be used in research papers that are focused on proposing or advocating for a particular viewpoint or policy. It involves presenting a strong editorial or opinion based on the research findings and offering recommendations or calls to action.

An externalizing conclusion is a type of conclusion that extends the research beyond the scope of the paper by suggesting potential future research directions or discussing the broader implications of the findings. This type of conclusion is often used in more theoretical or exploratory research papers.

Align your conclusion’s tone with the rest of your research paper. Start Writing with Paperpal Now!  

The conclusion in a research paper serves several important purposes:

• Offers Implications and Recommendations : Your research paper conclusion is an excellent place to discuss the broader implications of your research and suggest potential areas for further study. It’s also an opportunity to offer practical recommendations based on your findings.
• Provides Closure : A good research paper conclusion provides a sense of closure to your paper. It should leave the reader with a feeling that they have reached the end of a well-structured and thought-provoking research project.
• Leaves a Lasting Impression : Writing a well-crafted research paper conclusion leaves a lasting impression on your readers. It’s your final opportunity to leave them with a new idea, a call to action, or a memorable quote.

Writing a strong conclusion for your research paper is essential to leave a lasting impression on your readers. Here’s a step-by-step process to help you create and know what to put in the conclusion of a research paper: 2

• Research Statement : Begin your research paper conclusion by restating your research statement. This reminds the reader of the main point you’ve been trying to prove throughout your paper. Keep it concise and clear.
• Key Points : Summarize the main arguments and key points you’ve made in your paper. Avoid introducing new information in the research paper conclusion. Instead, provide a concise overview of what you’ve discussed in the body of your paper.
• Address the Research Questions : If your research paper is based on specific research questions or hypotheses, briefly address whether you’ve answered them or achieved your research goals. Discuss the significance of your findings in this context.
• Significance : Highlight the importance of your research and its relevance in the broader context. Explain why your findings matter and how they contribute to the existing knowledge in your field.
• Implications : Explore the practical or theoretical implications of your research. How might your findings impact future research, policy, or real-world applications? Consider the “so what?” question.
• Future Research : Offer suggestions for future research in your area. What questions or aspects remain unanswered or warrant further investigation? This shows that your work opens the door for future exploration.
• Closing Thought : Conclude your research paper conclusion with a thought-provoking or memorable statement. This can leave a lasting impression on your readers and wrap up your paper effectively. Avoid introducing new information or arguments here.
• Proofread and Revise : Carefully proofread your conclusion for grammar, spelling, and clarity. Ensure that your ideas flow smoothly and that your conclusion is coherent and well-structured.

Write your research paper conclusion 2x faster with Paperpal. Try it now!

Remember that a well-crafted research paper conclusion is a reflection of the strength of your research and your ability to communicate its significance effectively. It should leave a lasting impression on your readers and tie together all the threads of your paper. Now you know how to start the conclusion of a research paper and what elements to include to make it impactful, let’s look at a research paper conclusion sample.

How to write a research paper conclusion with Paperpal?

A research paper conclusion is not just a summary of your study, but a synthesis of the key findings that ties the research together and places it in a broader context. A research paper conclusion should be concise, typically around one paragraph in length. However, some complex topics may require a longer conclusion to ensure the reader is left with a clear understanding of the study’s significance. Paperpal, an AI writing assistant trusted by over 800,000 academics globally, can help you write a well-structured conclusion for your research paper. 

• Sign Up or Log In: Create a new Paperpal account or login with your details.  
• Navigate to Features : Once logged in, head over to the features’ side navigation pane. Click on Templates and you’ll find a suite of generative AI features to help you write better, faster.  
• Generate an outline: Under Templates, select ‘Outlines’. Choose ‘Research article’ as your document type.  
• Select your section: Since you’re focusing on the conclusion, select this section when prompted.  
• Choose your field of study: Identifying your field of study allows Paperpal to provide more targeted suggestions, ensuring the relevance of your conclusion to your specific area of research. 
• Provide a brief description of your study: Enter details about your research topic and findings. This information helps Paperpal generate a tailored outline that aligns with your paper’s content. 
• Generate the conclusion outline: After entering all necessary details, click on ‘generate’. Paperpal will then create a structured outline for your conclusion, to help you start writing and build upon the outline.  
• Write your conclusion: Use the generated outline to build your conclusion. The outline serves as a guide, ensuring you cover all critical aspects of a strong conclusion, from summarizing key findings to highlighting the research’s implications. 
• Refine and enhance: Paperpal’s ‘Make Academic’ feature can be particularly useful in the final stages. Select any paragraph of your conclusion and use this feature to elevate the academic tone, ensuring your writing is aligned to the academic journal standards. 

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The research paper conclusion is a crucial part of your paper as it provides the final opportunity to leave a strong impression on your readers. In the research paper conclusion, summarize the main points of your research paper by restating your research statement, highlighting the most important findings, addressing the research questions or objectives, explaining the broader context of the study, discussing the significance of your findings, providing recommendations if applicable, and emphasizing the takeaway message. The main purpose of the conclusion is to remind the reader of the main point or argument of your paper and to provide a clear and concise summary of the key findings and their implications. All these elements should feature on your list of what to put in the conclusion of a research paper to create a strong final statement for your work.

A strong conclusion is a critical component of a research paper, as it provides an opportunity to wrap up your arguments, reiterate your main points, and leave a lasting impression on your readers. Here are the key elements of a strong research paper conclusion: 1. Conciseness : A research paper conclusion should be concise and to the point. It should not introduce new information or ideas that were not discussed in the body of the paper. 2. Summarization : The research paper conclusion should be comprehensive enough to give the reader a clear understanding of the research’s main contributions. 3 . Relevance : Ensure that the information included in the research paper conclusion is directly relevant to the research paper’s main topic and objectives; avoid unnecessary details. 4 . Connection to the Introduction : A well-structured research paper conclusion often revisits the key points made in the introduction and shows how the research has addressed the initial questions or objectives. 5. Emphasis : Highlight the significance and implications of your research. Why is your study important? What are the broader implications or applications of your findings? 6 . Call to Action : Include a call to action or a recommendation for future research or action based on your findings.

The length of a research paper conclusion can vary depending on several factors, including the overall length of the paper, the complexity of the research, and the specific journal requirements. While there is no strict rule for the length of a conclusion, but it’s generally advisable to keep it relatively short. A typical research paper conclusion might be around 5-10% of the paper’s total length. For example, if your paper is 10 pages long, the conclusion might be roughly half a page to one page in length.

In general, you do not need to include citations in the research paper conclusion. Citations are typically reserved for the body of the paper to support your arguments and provide evidence for your claims. However, there may be some exceptions to this rule: 1. If you are drawing a direct quote or paraphrasing a specific source in your research paper conclusion, you should include a citation to give proper credit to the original author. 2. If your conclusion refers to or discusses specific research, data, or sources that are crucial to the overall argument, citations can be included to reinforce your conclusion’s validity.

The conclusion of a research paper serves several important purposes: 1. Summarize the Key Points 2. Reinforce the Main Argument 3. Provide Closure 4. Offer Insights or Implications 5. Engage the Reader. 6. Reflect on Limitations

Remember that the primary purpose of the research paper conclusion is to leave a lasting impression on the reader, reinforcing the key points and providing closure to your research. It’s often the last part of the paper that the reader will see, so it should be strong and well-crafted.

• Makar, G., Foltz, C., Lendner, M., & Vaccaro, A. R. (2018). How to write effective discussion and conclusion sections. Clinical spine surgery, 31(8), 345-346.
• Bunton, D. (2005). The structure of PhD conclusion chapters.  Journal of English for academic purposes ,  4 (3), 207-224.

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Cochrane Training

Chapter 15: interpreting results and drawing conclusions.

Holger J Schünemann, Gunn E Vist, Julian PT Higgins, Nancy Santesso, Jonathan J Deeks, Paul Glasziou, Elie A Akl, Gordon H Guyatt; on behalf of the Cochrane GRADEing Methods Group

Key Points:

• This chapter provides guidance on interpreting the results of synthesis in order to communicate the conclusions of the review effectively.
• Methods are presented for computing, presenting and interpreting relative and absolute effects for dichotomous outcome data, including the number needed to treat (NNT).
• For continuous outcome measures, review authors can present summary results for studies using natural units of measurement or as minimal important differences when all studies use the same scale. When studies measure the same construct but with different scales, review authors will need to find a way to interpret the standardized mean difference, or to use an alternative effect measure for the meta-analysis such as the ratio of means.
• Review authors should not describe results as ‘statistically significant’, ‘not statistically significant’ or ‘non-significant’ or unduly rely on thresholds for P values, but report the confidence interval together with the exact P value.
• Review authors should not make recommendations about healthcare decisions, but they can – after describing the certainty of evidence and the balance of benefits and harms – highlight different actions that might be consistent with particular patterns of values and preferences and other factors that determine a decision such as cost.

Cite this chapter as: Schünemann HJ, Vist GE, Higgins JPT, Santesso N, Deeks JJ, Glasziou P, Akl EA, Guyatt GH. Chapter 15: Interpreting results and drawing conclusions [last updated August 2023]. In: Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA (editors). Cochrane Handbook for Systematic Reviews of Interventions version 6.5. Cochrane, 2024. Available from www.training.cochrane.org/handbook .

15.1 Introduction

The purpose of Cochrane Reviews is to facilitate healthcare decisions by patients and the general public, clinicians, guideline developers, administrators and policy makers. They also inform future research. A clear statement of findings, a considered discussion and a clear presentation of the authors’ conclusions are, therefore, important parts of the review. In particular, the following issues can help people make better informed decisions and increase the usability of Cochrane Reviews:

• information on all important outcomes, including adverse outcomes;
• the certainty of the evidence for each of these outcomes, as it applies to specific populations and specific interventions; and
• clarification of the manner in which particular values and preferences may bear on the desirable and undesirable consequences of the intervention.

A ‘Summary of findings’ table, described in Chapter 14 , Section 14.1 , provides key pieces of information about health benefits and harms in a quick and accessible format. It is highly desirable that review authors include a ‘Summary of findings’ table in Cochrane Reviews alongside a sufficient description of the studies and meta-analyses to support its contents. This description includes the rating of the certainty of evidence, also called the quality of the evidence or confidence in the estimates of the effects, which is expected in all Cochrane Reviews.

‘Summary of findings’ tables are usually supported by full evidence profiles which include the detailed ratings of the evidence (Guyatt et al 2011a, Guyatt et al 2013a, Guyatt et al 2013b, Santesso et al 2016). The Discussion section of the text of the review provides space to reflect and consider the implications of these aspects of the review’s findings. Cochrane Reviews include five standard subheadings to ensure the Discussion section places the review in an appropriate context: ‘Summary of main results (benefits and harms)’; ‘Potential biases in the review process’; ‘Overall completeness and applicability of evidence’; ‘Certainty of the evidence’; and ‘Agreements and disagreements with other studies or reviews’. Following the Discussion, the Authors’ conclusions section is divided into two standard subsections: ‘Implications for practice’ and ‘Implications for research’. The assessment of the certainty of evidence facilitates a structured description of the implications for practice and research.

Because Cochrane Reviews have an international audience, the Discussion and Authors’ conclusions should, so far as possible, assume a broad international perspective and provide guidance for how the results could be applied in different settings, rather than being restricted to specific national or local circumstances. Cultural differences and economic differences may both play an important role in determining the best course of action based on the results of a Cochrane Review. Furthermore, individuals within societies have widely varying values and preferences regarding health states, and use of societal resources to achieve particular health states. For all these reasons, and because information that goes beyond that included in a Cochrane Review is required to make fully informed decisions, different people will often make different decisions based on the same evidence presented in a review.

Thus, review authors should avoid specific recommendations that inevitably depend on assumptions about available resources, values and preferences, and other factors such as equity considerations, feasibility and acceptability of an intervention. The purpose of the review should be to present information and aid interpretation rather than to offer recommendations. The discussion and conclusions should help people understand the implications of the evidence in relation to practical decisions and apply the results to their specific situation. Review authors can aid this understanding of the implications by laying out different scenarios that describe certain value structures.

In this chapter, we address first one of the key aspects of interpreting findings that is also fundamental in completing a ‘Summary of findings’ table: the certainty of evidence related to each of the outcomes. We then provide a more detailed consideration of issues around applicability and around interpretation of numerical results, and provide suggestions for presenting authors’ conclusions.

15.2 Issues of indirectness and applicability

15.2.1 the role of the review author.

“A leap of faith is always required when applying any study findings to the population at large” or to a specific person. “In making that jump, one must always strike a balance between making justifiable broad generalizations and being too conservative in one’s conclusions” (Friedman et al 1985). In addition to issues about risk of bias and other domains determining the certainty of evidence, this leap of faith is related to how well the identified body of evidence matches the posed PICO ( Population, Intervention, Comparator(s) and Outcome ) question. As to the population, no individual can be entirely matched to the population included in research studies. At the time of decision, there will always be differences between the study population and the person or population to whom the evidence is applied; sometimes these differences are slight, sometimes large.

The terms applicability, generalizability, external validity and transferability are related, sometimes used interchangeably and have in common that they lack a clear and consistent definition in the classic epidemiological literature (Schünemann et al 2013). However, all of the terms describe one overarching theme: whether or not available research evidence can be directly used to answer the health and healthcare question at hand, ideally supported by a judgement about the degree of confidence in this use (Schünemann et al 2013). GRADE’s certainty domains include a judgement about ‘indirectness’ to describe all of these aspects including the concept of direct versus indirect comparisons of different interventions (Atkins et al 2004, Guyatt et al 2008, Guyatt et al 2011b).

To address adequately the extent to which a review is relevant for the purpose to which it is being put, there are certain things the review author must do, and certain things the user of the review must do to assess the degree of indirectness. Cochrane and the GRADE Working Group suggest using a very structured framework to address indirectness. We discuss here and in Chapter 14 what the review author can do to help the user. Cochrane Review authors must be extremely clear on the population, intervention and outcomes that they intend to address. Chapter 14, Section 14.1.2 , also emphasizes a crucial step: the specification of all patient-important outcomes relevant to the intervention strategies under comparison.

In considering whether the effect of an intervention applies equally to all participants, and whether different variations on the intervention have similar effects, review authors need to make a priori hypotheses about possible effect modifiers, and then examine those hypotheses (see Chapter 10, Section 10.10 and Section 10.11 ). If they find apparent subgroup effects, they must ultimately decide whether or not these effects are credible (Sun et al 2012). Differences between subgroups, particularly those that correspond to differences between studies, should be interpreted cautiously. Some chance variation between subgroups is inevitable so, unless there is good reason to believe that there is an interaction, review authors should not assume that the subgroup effect exists. If, despite due caution, review authors judge subgroup effects in terms of relative effect estimates as credible (i.e. the effects differ credibly), they should conduct separate meta-analyses for the relevant subgroups, and produce separate ‘Summary of findings’ tables for those subgroups.

The user of the review will be challenged with ‘individualization’ of the findings, whether they seek to apply the findings to an individual patient or a policy decision in a specific context. For example, even if relative effects are similar across subgroups, absolute effects will differ according to baseline risk. Review authors can help provide this information by identifying identifiable groups of people with varying baseline risks in the ‘Summary of findings’ tables, as discussed in Chapter 14, Section 14.1.3 . Users can then identify their specific case or population as belonging to a particular risk group, if relevant, and assess their likely magnitude of benefit or harm accordingly. A description of the identifying prognostic or baseline risk factors in a brief scenario (e.g. age or gender) will help users of a review further.

Another decision users must make is whether their individual case or population of interest is so different from those included in the studies that they cannot use the results of the systematic review and meta-analysis at all. Rather than rigidly applying the inclusion and exclusion criteria of studies, it is better to ask whether or not there are compelling reasons why the evidence should not be applied to a particular patient. Review authors can sometimes help decision makers by identifying important variation where divergence might limit the applicability of results (Rothwell 2005, Schünemann et al 2006, Guyatt et al 2011b, Schünemann et al 2013), including biologic and cultural variation, and variation in adherence to an intervention.

In addressing these issues, review authors cannot be aware of, or address, the myriad of differences in circumstances around the world. They can, however, address differences of known importance to many people and, importantly, they should avoid assuming that other people’s circumstances are the same as their own in discussing the results and drawing conclusions.

15.2.2 Biological variation

Issues of biological variation that may affect the applicability of a result to a reader or population include divergence in pathophysiology (e.g. biological differences between women and men that may affect responsiveness to an intervention) and divergence in a causative agent (e.g. for infectious diseases such as malaria, which may be caused by several different parasites). The discussion of the results in the review should make clear whether the included studies addressed all or only some of these groups, and whether any important subgroup effects were found.

15.2.3 Variation in context

Some interventions, particularly non-pharmacological interventions, may work in some contexts but not in others; the situation has been described as program by context interaction (Hawe et al 2004). Contextual factors might pertain to the host organization in which an intervention is offered, such as the expertise, experience and morale of the staff expected to carry out the intervention, the competing priorities for the clinician’s or staff’s attention, the local resources such as service and facilities made available to the program and the status or importance given to the program by the host organization. Broader context issues might include aspects of the system within which the host organization operates, such as the fee or payment structure for healthcare providers and the local insurance system. Some interventions, in particular complex interventions (see Chapter 17 ), can be only partially implemented in some contexts, and this requires judgements about indirectness of the intervention and its components for readers in that context (Schünemann 2013).

Contextual factors may also pertain to the characteristics of the target group or population, such as cultural and linguistic diversity, socio-economic position, rural/urban setting. These factors may mean that a particular style of care or relationship evolves between service providers and consumers that may or may not match the values and technology of the program.

For many years these aspects have been acknowledged when decision makers have argued that results of evidence reviews from other countries do not apply in their own country or setting. Whilst some programmes/interventions have been successfully transferred from one context to another, others have not (Resnicow et al 1993, Lumley et al 2004, Coleman et al 2015). Review authors should be cautious when making generalizations from one context to another. They should report on the presence (or otherwise) of context-related information in intervention studies, where this information is available.

15.2.4 Variation in adherence

Variation in the adherence of the recipients and providers of care can limit the certainty in the applicability of results. Predictable differences in adherence can be due to divergence in how recipients of care perceive the intervention (e.g. the importance of side effects), economic conditions or attitudes that make some forms of care inaccessible in some settings, such as in low-income countries (Dans et al 2007). It should not be assumed that high levels of adherence in closely monitored randomized trials will translate into similar levels of adherence in normal practice.

15.2.5 Variation in values and preferences

Decisions about healthcare management strategies and options involve trading off health benefits and harms. The right choice may differ for people with different values and preferences (i.e. the importance people place on the outcomes and interventions), and it is important that decision makers ensure that decisions are consistent with a patient or population’s values and preferences. The importance placed on outcomes, together with other factors, will influence whether the recipients of care will or will not accept an option that is offered (Alonso-Coello et al 2016) and, thus, can be one factor influencing adherence. In Section 15.6 , we describe how the review author can help this process and the limits of supporting decision making based on intervention reviews.

15.3 Interpreting results of statistical analyses

15.3.1 confidence intervals.

Results for both individual studies and meta-analyses are reported with a point estimate together with an associated confidence interval. For example, ‘The odds ratio was 0.75 with a 95% confidence interval of 0.70 to 0.80’. The point estimate (0.75) is the best estimate of the magnitude and direction of the experimental intervention’s effect compared with the comparator intervention. The confidence interval describes the uncertainty inherent in any estimate, and describes a range of values within which we can be reasonably sure that the true effect actually lies. If the confidence interval is relatively narrow (e.g. 0.70 to 0.80), the effect size is known precisely. If the interval is wider (e.g. 0.60 to 0.93) the uncertainty is greater, although there may still be enough precision to make decisions about the utility of the intervention. Intervals that are very wide (e.g. 0.50 to 1.10) indicate that we have little knowledge about the effect and this imprecision affects our certainty in the evidence, and that further information would be needed before we could draw a more certain conclusion.

A 95% confidence interval is often interpreted as indicating a range within which we can be 95% certain that the true effect lies. This statement is a loose interpretation, but is useful as a rough guide. The strictly correct interpretation of a confidence interval is based on the hypothetical notion of considering the results that would be obtained if the study were repeated many times. If a study were repeated infinitely often, and on each occasion a 95% confidence interval calculated, then 95% of these intervals would contain the true effect (see Section 15.3.3 for further explanation).

The width of the confidence interval for an individual study depends to a large extent on the sample size. Larger studies tend to give more precise estimates of effects (and hence have narrower confidence intervals) than smaller studies. For continuous outcomes, precision depends also on the variability in the outcome measurements (i.e. how widely individual results vary between people in the study, measured as the standard deviation); for dichotomous outcomes it depends on the risk of the event (more frequent events allow more precision, and narrower confidence intervals), and for time-to-event outcomes it also depends on the number of events observed. All these quantities are used in computation of the standard errors of effect estimates from which the confidence interval is derived.

The width of a confidence interval for a meta-analysis depends on the precision of the individual study estimates and on the number of studies combined. In addition, for random-effects models, precision will decrease with increasing heterogeneity and confidence intervals will widen correspondingly (see Chapter 10, Section 10.10.4 ). As more studies are added to a meta-analysis the width of the confidence interval usually decreases. However, if the additional studies increase the heterogeneity in the meta-analysis and a random-effects model is used, it is possible that the confidence interval width will increase.

Confidence intervals and point estimates have different interpretations in fixed-effect and random-effects models. While the fixed-effect estimate and its confidence interval address the question ‘what is the best (single) estimate of the effect?’, the random-effects estimate assumes there to be a distribution of effects, and the estimate and its confidence interval address the question ‘what is the best estimate of the average effect?’ A confidence interval may be reported for any level of confidence (although they are most commonly reported for 95%, and sometimes 90% or 99%). For example, the odds ratio of 0.80 could be reported with an 80% confidence interval of 0.73 to 0.88; a 90% interval of 0.72 to 0.89; and a 95% interval of 0.70 to 0.92. As the confidence level increases, the confidence interval widens.

There is logical correspondence between the confidence interval and the P value (see Section 15.3.3 ). The 95% confidence interval for an effect will exclude the null value (such as an odds ratio of 1.0 or a risk difference of 0) if and only if the test of significance yields a P value of less than 0.05. If the P value is exactly 0.05, then either the upper or lower limit of the 95% confidence interval will be at the null value. Similarly, the 99% confidence interval will exclude the null if and only if the test of significance yields a P value of less than 0.01.

Together, the point estimate and confidence interval provide information to assess the effects of the intervention on the outcome. For example, suppose that we are evaluating an intervention that reduces the risk of an event and we decide that it would be useful only if it reduced the risk of an event from 30% by at least 5 percentage points to 25% (these values will depend on the specific clinical scenario and outcomes, including the anticipated harms). If the meta-analysis yielded an effect estimate of a reduction of 10 percentage points with a tight 95% confidence interval, say, from 7% to 13%, we would be able to conclude that the intervention was useful since both the point estimate and the entire range of the interval exceed our criterion of a reduction of 5% for net health benefit. However, if the meta-analysis reported the same risk reduction of 10% but with a wider interval, say, from 2% to 18%, although we would still conclude that our best estimate of the intervention effect is that it provides net benefit, we could not be so confident as we still entertain the possibility that the effect could be between 2% and 5%. If the confidence interval was wider still, and included the null value of a difference of 0%, we would still consider the possibility that the intervention has no effect on the outcome whatsoever, and would need to be even more sceptical in our conclusions.

Review authors may use the same general approach to conclude that an intervention is not useful. Continuing with the above example where the criterion for an important difference that should be achieved to provide more benefit than harm is a 5% risk difference, an effect estimate of 2% with a 95% confidence interval of 1% to 4% suggests that the intervention does not provide net health benefit.

15.3.2 P values and statistical significance

A P value is the standard result of a statistical test, and is the probability of obtaining the observed effect (or larger) under a ‘null hypothesis’. In the context of Cochrane Reviews there are two commonly used statistical tests. The first is a test of overall effect (a Z-test), and its null hypothesis is that there is no overall effect of the experimental intervention compared with the comparator on the outcome of interest. The second is the (Chi 2 ) test for heterogeneity, and its null hypothesis is that there are no differences in the intervention effects across studies.

A P value that is very small indicates that the observed effect is very unlikely to have arisen purely by chance, and therefore provides evidence against the null hypothesis. It has been common practice to interpret a P value by examining whether it is smaller than particular threshold values. In particular, P values less than 0.05 are often reported as ‘statistically significant’, and interpreted as being small enough to justify rejection of the null hypothesis. However, the 0.05 threshold is an arbitrary one that became commonly used in medical and psychological research largely because P values were determined by comparing the test statistic against tabulations of specific percentage points of statistical distributions. If review authors decide to present a P value with the results of a meta-analysis, they should report a precise P value (as calculated by most statistical software), together with the 95% confidence interval. Review authors should not describe results as ‘statistically significant’, ‘not statistically significant’ or ‘non-significant’ or unduly rely on thresholds for P values , but report the confidence interval together with the exact P value (see MECIR Box 15.3.a ).

We discuss interpretation of the test for heterogeneity in Chapter 10, Section 10.10.2 ; the remainder of this section refers mainly to tests for an overall effect. For tests of an overall effect, the computation of P involves both the effect estimate and precision of the effect estimate (driven largely by sample size). As precision increases, the range of plausible effects that could occur by chance is reduced. Correspondingly, the statistical significance of an effect of a particular magnitude will usually be greater (the P value will be smaller) in a larger study than in a smaller study.

P values are commonly misinterpreted in two ways. First, a moderate or large P value (e.g. greater than 0.05) may be misinterpreted as evidence that the intervention has no effect on the outcome. There is an important difference between this statement and the correct interpretation that there is a high probability that the observed effect on the outcome is due to chance alone. To avoid such a misinterpretation, review authors should always examine the effect estimate and its 95% confidence interval.

The second misinterpretation is to assume that a result with a small P value for the summary effect estimate implies that an experimental intervention has an important benefit. Such a misinterpretation is more likely to occur in large studies and meta-analyses that accumulate data over dozens of studies and thousands of participants. The P value addresses the question of whether the experimental intervention effect is precisely nil; it does not examine whether the effect is of a magnitude of importance to potential recipients of the intervention. In a large study, a small P value may represent the detection of a trivial effect that may not lead to net health benefit when compared with the potential harms (i.e. harmful effects on other important outcomes). Again, inspection of the point estimate and confidence interval helps correct interpretations (see Section 15.3.1 ).

MECIR Box 15.3.a Relevant expectations for conduct of intervention reviews

15.3.3 Relation between confidence intervals, statistical significance and certainty of evidence

The confidence interval (and imprecision) is only one domain that influences overall uncertainty about effect estimates. Uncertainty resulting from imprecision (i.e. statistical uncertainty) may be no less important than uncertainty from indirectness, or any other GRADE domain, in the context of decision making (Schünemann 2016). Thus, the extent to which interpretations of the confidence interval described in Sections 15.3.1 and 15.3.2 correspond to conclusions about overall certainty of the evidence for the outcome of interest depends on these other domains. If there are no concerns about other domains that determine the certainty of the evidence (i.e. risk of bias, inconsistency, indirectness or publication bias), then the interpretation in Sections 15.3.1 and 15.3.2 . about the relation of the confidence interval to the true effect may be carried forward to the overall certainty. However, if there are concerns about the other domains that affect the certainty of the evidence, the interpretation about the true effect needs to be seen in the context of further uncertainty resulting from those concerns.

For example, nine randomized controlled trials in almost 6000 cancer patients indicated that the administration of heparin reduces the risk of venous thromboembolism (VTE), with a risk ratio of 43% (95% CI 19% to 60%) (Akl et al 2011a). For patients with a plausible baseline risk of approximately 4.6% per year, this relative effect suggests that heparin leads to an absolute risk reduction of 20 fewer VTEs (95% CI 9 fewer to 27 fewer) per 1000 people per year (Akl et al 2011a). Now consider that the review authors or those applying the evidence in a guideline have lowered the certainty in the evidence as a result of indirectness. While the confidence intervals would remain unchanged, the certainty in that confidence interval and in the point estimate as reflecting the truth for the question of interest will be lowered. In fact, the certainty range will have unknown width so there will be unknown likelihood of a result within that range because of this indirectness. The lower the certainty in the evidence, the less we know about the width of the certainty range, although methods for quantifying risk of bias and understanding potential direction of bias may offer insight when lowered certainty is due to risk of bias. Nevertheless, decision makers must consider this uncertainty, and must do so in relation to the effect measure that is being evaluated (e.g. a relative or absolute measure). We will describe the impact on interpretations for dichotomous outcomes in Section 15.4 .

15.4 Interpreting results from dichotomous outcomes (including numbers needed to treat)

15.4.1 relative and absolute risk reductions.

Clinicians may be more inclined to prescribe an intervention that reduces the relative risk of death by 25% than one that reduces the risk of death by 1 percentage point, although both presentations of the evidence may relate to the same benefit (i.e. a reduction in risk from 4% to 3%). The former refers to the relative reduction in risk and the latter to the absolute reduction in risk. As described in Chapter 6, Section 6.4.1 , there are several measures for comparing dichotomous outcomes in two groups. Meta-analyses are usually undertaken using risk ratios (RR), odds ratios (OR) or risk differences (RD), but there are several alternative ways of expressing results.

Relative risk reduction (RRR) is a convenient way of re-expressing a risk ratio as a percentage reduction:

For example, a risk ratio of 0.75 translates to a relative risk reduction of 25%, as in the example above.

The risk difference is often referred to as the absolute risk reduction (ARR) or absolute risk increase (ARI), and may be presented as a percentage (e.g. 1%), as a decimal (e.g. 0.01), or as account (e.g. 10 out of 1000). We consider different choices for presenting absolute effects in Section 15.4.3 . We then describe computations for obtaining these numbers from the results of individual studies and of meta-analyses in Section 15.4.4 .

15.4.2 Number needed to treat (NNT)

The number needed to treat (NNT) is a common alternative way of presenting information on the effect of an intervention. The NNT is defined as the expected number of people who need to receive the experimental rather than the comparator intervention for one additional person to either incur or avoid an event (depending on the direction of the result) in a given time frame. Thus, for example, an NNT of 10 can be interpreted as ‘it is expected that one additional (or less) person will incur an event for every 10 participants receiving the experimental intervention rather than comparator over a given time frame’. It is important to be clear that:

• since the NNT is derived from the risk difference, it is still a comparative measure of effect (experimental versus a specific comparator) and not a general property of a single intervention; and
• the NNT gives an ‘expected value’. For example, NNT = 10 does not imply that one additional event will occur in each and every group of 10 people.

NNTs can be computed for both beneficial and detrimental events, and for interventions that cause both improvements and deteriorations in outcomes. In all instances NNTs are expressed as positive whole numbers. Some authors use the term ‘number needed to harm’ (NNH) when an intervention leads to an adverse outcome, or a decrease in a positive outcome, rather than improvement. However, this phrase can be misleading (most notably, it can easily be read to imply the number of people who will experience a harmful outcome if given the intervention), and it is strongly recommended that ‘number needed to harm’ and ‘NNH’ are avoided. The preferred alternative is to use phrases such as ‘number needed to treat for an additional beneficial outcome’ (NNTB) and ‘number needed to treat for an additional harmful outcome’ (NNTH) to indicate direction of effect.

As NNTs refer to events, their interpretation needs to be worded carefully when the binary outcome is a dichotomization of a scale-based outcome. For example, if the outcome is pain measured on a ‘none, mild, moderate or severe’ scale it may have been dichotomized as ‘none or mild’ versus ‘moderate or severe’. It would be inappropriate for an NNT from these data to be referred to as an ‘NNT for pain’. It is an ‘NNT for moderate or severe pain’.

We consider different choices for presenting absolute effects in Section 15.4.3 . We then describe computations for obtaining these numbers from the results of individual studies and of meta-analyses in Section 15.4.4 .

15.4.3 Expressing risk differences

Users of reviews are liable to be influenced by the choice of statistical presentations of the evidence. Hoffrage and colleagues suggest that physicians’ inferences about statistical outcomes are more appropriate when they deal with ‘natural frequencies’ – whole numbers of people, both treated and untreated (e.g. treatment results in a drop from 20 out of 1000 to 10 out of 1000 women having breast cancer) – than when effects are presented as percentages (e.g. 1% absolute reduction in breast cancer risk) (Hoffrage et al 2000). Probabilities may be more difficult to understand than frequencies, particularly when events are rare. While standardization may be important in improving the presentation of research evidence (and participation in healthcare decisions), current evidence suggests that the presentation of natural frequencies for expressing differences in absolute risk is best understood by consumers of healthcare information (Akl et al 2011b). This evidence provides the rationale for presenting absolute risks in ‘Summary of findings’ tables as numbers of people with events per 1000 people receiving the intervention (see Chapter 14 ).

RRs and RRRs remain crucial because relative effects tend to be substantially more stable across risk groups than absolute effects (see Chapter 10, Section 10.4.3 ). Review authors can use their own data to study this consistency (Cates 1999, Smeeth et al 1999). Risk differences from studies are least likely to be consistent across baseline event rates; thus, they are rarely appropriate for computing numbers needed to treat in systematic reviews. If a relative effect measure (OR or RR) is chosen for meta-analysis, then a comparator group risk needs to be specified as part of the calculation of an RD or NNT. In addition, if there are several different groups of participants with different levels of risk, it is crucial to express absolute benefit for each clinically identifiable risk group, clarifying the time period to which this applies. Studies in patients with differing severity of disease, or studies with different lengths of follow-up will almost certainly have different comparator group risks. In these cases, different comparator group risks lead to different RDs and NNTs (except when the intervention has no effect). A recommended approach is to re-express an odds ratio or a risk ratio as a variety of RD or NNTs across a range of assumed comparator risks (ACRs) (McQuay and Moore 1997, Smeeth et al 1999). Review authors should bear these considerations in mind not only when constructing their ‘Summary of findings’ table, but also in the text of their review.

For example, a review of oral anticoagulants to prevent stroke presented information to users by describing absolute benefits for various baseline risks (Aguilar and Hart 2005, Aguilar et al 2007). They presented their principal findings as “The inherent risk of stroke should be considered in the decision to use oral anticoagulants in atrial fibrillation patients, selecting those who stand to benefit most for this therapy” (Aguilar and Hart 2005). Among high-risk atrial fibrillation patients with prior stroke or transient ischaemic attack who have stroke rates of about 12% (120 per 1000) per year, warfarin prevents about 70 strokes yearly per 1000 patients, whereas for low-risk atrial fibrillation patients (with a stroke rate of about 2% per year or 20 per 1000), warfarin prevents only 12 strokes. This presentation helps users to understand the important impact that typical baseline risks have on the absolute benefit that they can expect.

15.4.4 Computations

Direct computation of risk difference (RD) or a number needed to treat (NNT) depends on the summary statistic (odds ratio, risk ratio or risk differences) available from the study or meta-analysis. When expressing results of meta-analyses, review authors should use, in the computations, whatever statistic they determined to be the most appropriate summary for meta-analysis (see Chapter 10, Section 10.4.3 ). Here we present calculations to obtain RD as a reduction in the number of participants per 1000. For example, a risk difference of –0.133 corresponds to 133 fewer participants with the event per 1000.

RDs and NNTs should not be computed from the aggregated total numbers of participants and events across the trials. This approach ignores the randomization within studies, and may produce seriously misleading results if there is unbalanced randomization in any of the studies. Using the pooled result of a meta-analysis is more appropriate. When computing NNTs, the values obtained are by convention always rounded up to the next whole number.

15.4.4.1 Computing NNT from a risk difference (RD)

A NNT may be computed from a risk difference as

where the vertical bars (‘absolute value of’) in the denominator indicate that any minus sign should be ignored. It is convention to round the NNT up to the nearest whole number. For example, if the risk difference is –0.12 the NNT is 9; if the risk difference is –0.22 the NNT is 5. Cochrane Review authors should qualify the NNT as referring to benefit (improvement) or harm by denoting the NNT as NNTB or NNTH. Note that this approach, although feasible, should be used only for the results of a meta-analysis of risk differences. In most cases meta-analyses will be undertaken using a relative measure of effect (RR or OR), and those statistics should be used to calculate the NNT (see Section 15.4.4.2 and 15.4.4.3 ).

15.4.4.2 Computing risk differences or NNT from a risk ratio

To aid interpretation of the results of a meta-analysis of risk ratios, review authors may compute an absolute risk reduction or NNT. In order to do this, an assumed comparator risk (ACR) (otherwise known as a baseline risk, or risk that the outcome of interest would occur with the comparator intervention) is required. It will usually be appropriate to do this for a range of different ACRs. The computation proceeds as follows:

As an example, suppose the risk ratio is RR = 0.92, and an ACR = 0.3 (300 per 1000) is assumed. Then the effect on risk is 24 fewer per 1000:

The NNT is 42:

15.4.4.3 Computing risk differences or NNT from an odds ratio

Review authors may wish to compute a risk difference or NNT from the results of a meta-analysis of odds ratios. In order to do this, an ACR is required. It will usually be appropriate to do this for a range of different ACRs. The computation proceeds as follows:

As an example, suppose the odds ratio is OR = 0.73, and a comparator risk of ACR = 0.3 is assumed. Then the effect on risk is 62 fewer per 1000:

The NNT is 17:

15.4.4.4 Computing risk ratio from an odds ratio

Because risk ratios are easier to interpret than odds ratios, but odds ratios have favourable mathematical properties, a review author may decide to undertake a meta-analysis based on odds ratios, but to express the result as a summary risk ratio (or relative risk reduction). This requires an ACR. Then

It will often be reasonable to perform this transformation using the median comparator group risk from the studies in the meta-analysis.

15.4.4.5 Computing confidence limits

Confidence limits for RDs and NNTs may be calculated by applying the above formulae to the upper and lower confidence limits for the summary statistic (RD, RR or OR) (Altman 1998). Note that this confidence interval does not incorporate uncertainty around the ACR.

If the 95% confidence interval of OR or RR includes the value 1, one of the confidence limits will indicate benefit and the other harm. Thus, appropriate use of the words ‘fewer’ and ‘more’ is required for each limit when presenting results in terms of events. For NNTs, the two confidence limits should be labelled as NNTB and NNTH to indicate the direction of effect in each case. The confidence interval for the NNT will include a ‘discontinuity’, because increasingly smaller risk differences that approach zero will lead to NNTs approaching infinity. Thus, the confidence interval will include both an infinitely large NNTB and an infinitely large NNTH.

15.5 Interpreting results from continuous outcomes (including standardized mean differences)

15.5.1 meta-analyses with continuous outcomes.

Review authors should describe in the study protocol how they plan to interpret results for continuous outcomes. When outcomes are continuous, review authors have a number of options to present summary results. These options differ if studies report the same measure that is familiar to the target audiences, studies report the same or very similar measures that are less familiar to the target audiences, or studies report different measures.

15.5.2 Meta-analyses with continuous outcomes using the same measure

If all studies have used the same familiar units, for instance, results are expressed as durations of events, such as symptoms for conditions including diarrhoea, sore throat, otitis media, influenza or duration of hospitalization, a meta-analysis may generate a summary estimate in those units, as a difference in mean response (see, for instance, the row summarizing results for duration of diarrhoea in Chapter 14, Figure 14.1.b and the row summarizing oedema in Chapter 14, Figure 14.1.a ). For such outcomes, the ‘Summary of findings’ table should include a difference of means between the two interventions. However, when units of such outcomes may be difficult to interpret, particularly when they relate to rating scales (again, see the oedema row of Chapter 14, Figure 14.1.a ). ‘Summary of findings’ tables should include the minimum and maximum of the scale of measurement, and the direction. Knowledge of the smallest change in instrument score that patients perceive is important – the minimal important difference (MID) – and can greatly facilitate the interpretation of results (Guyatt et al 1998, Schünemann and Guyatt 2005). Knowing the MID allows review authors and users to place results in context. Review authors should state the MID – if known – in the Comments column of their ‘Summary of findings’ table. For example, the chronic respiratory questionnaire has possible scores in health-related quality of life ranging from 1 to 7 and 0.5 represents a well-established MID (Jaeschke et al 1989, Schünemann et al 2005).

15.5.3 Meta-analyses with continuous outcomes using different measures

When studies have used different instruments to measure the same construct, a standardized mean difference (SMD) may be used in meta-analysis for combining continuous data. Without guidance, clinicians and patients may have little idea how to interpret results presented as SMDs. Review authors should therefore consider issues of interpretability when planning their analysis at the protocol stage and should consider whether there will be suitable ways to re-express the SMD or whether alternative effect measures, such as a ratio of means, or possibly as minimal important difference units (Guyatt et al 2013b) should be used. Table 15.5.a and the following sections describe these options.

Table 15.5.a Approaches and their implications to presenting results of continuous variables when primary studies have used different instruments to measure the same construct. Adapted from Guyatt et al (2013b)

15.5.3.1 Presenting and interpreting SMDs using generic effect size estimates

The SMD expresses the intervention effect in standard units rather than the original units of measurement. The SMD is the difference in mean effects between the experimental and comparator groups divided by the pooled standard deviation of participants’ outcomes, or external SDs when studies are very small (see Chapter 6, Section 6.5.1.2 ). The value of a SMD thus depends on both the size of the effect (the difference between means) and the standard deviation of the outcomes (the inherent variability among participants or based on an external SD).

If review authors use the SMD, they might choose to present the results directly as SMDs (row 1a, Table 15.5.a and Table 15.5.b ). However, absolute values of the intervention and comparison groups are typically not useful because studies have used different measurement instruments with different units. Guiding rules for interpreting SMDs (or ‘Cohen’s effect sizes’) exist, and have arisen mainly from researchers in the social sciences (Cohen 1988). One example is as follows: 0.2 represents a small effect, 0.5 a moderate effect and 0.8 a large effect (Cohen 1988). Variations exist (e.g. <0.40=small, 0.40 to 0.70=moderate, >0.70=large). Review authors might consider including such a guiding rule in interpreting the SMD in the text of the review, and in summary versions such as the Comments column of a ‘Summary of findings’ table. However, some methodologists believe that such interpretations are problematic because patient importance of a finding is context-dependent and not amenable to generic statements.

15.5.3.2 Re-expressing SMDs using a familiar instrument

The second possibility for interpreting the SMD is to express it in the units of one or more of the specific measurement instruments used by the included studies (row 1b, Table 15.5.a and Table 15.5.b ). The approach is to calculate an absolute difference in means by multiplying the SMD by an estimate of the SD associated with the most familiar instrument. To obtain this SD, a reasonable option is to calculate a weighted average across all intervention groups of all studies that used the selected instrument (preferably a pre-intervention or post-intervention SD as discussed in Chapter 10, Section 10.5.2 ). To better reflect among-person variation in practice, or to use an instrument not represented in the meta-analysis, it may be preferable to use a standard deviation from a representative observational study. The summary effect is thus re-expressed in the original units of that particular instrument and the clinical relevance and impact of the intervention effect can be interpreted using that familiar instrument.

The same approach of re-expressing the results for a familiar instrument can also be used for other standardized effect measures such as when standardizing by MIDs (Guyatt et al 2013b): see Section 15.5.3.5 .

Table 15.5.b Application of approaches when studies have used different measures: effects of dexamethasone for pain after laparoscopic cholecystectomy (Karanicolas et al 2008). Reproduced with permission of Wolters Kluwer

1 Certainty rated according to GRADE from very low to high certainty. 2 Substantial unexplained heterogeneity in study results. 3 Imprecision due to wide confidence intervals. 4 The 20% comes from the proportion in the control group requiring rescue analgesia. 5 Crude (arithmetic) means of the post-operative pain mean responses across all five trials when transformed to a 100-point scale.

15.5.3.3 Re-expressing SMDs through dichotomization and transformation to relative and absolute measures

A third approach (row 1c, Table 15.5.a and Table 15.5.b ) relies on converting the continuous measure into a dichotomy and thus allows calculation of relative and absolute effects on a binary scale. A transformation of a SMD to a (log) odds ratio is available, based on the assumption that an underlying continuous variable has a logistic distribution with equal standard deviation in the two intervention groups, as discussed in Chapter 10, Section 10.6  (Furukawa 1999, Guyatt et al 2013b). The assumption is unlikely to hold exactly and the results must be regarded as an approximation. The log odds ratio is estimated as

(or approximately 1.81✕SMD). The resulting odds ratio can then be presented as normal, and in a ‘Summary of findings’ table, combined with an assumed comparator group risk to be expressed as an absolute risk difference. The comparator group risk in this case would refer to the proportion of people who have achieved a specific value of the continuous outcome. In randomized trials this can be interpreted as the proportion who have improved by some (specified) amount (responders), for instance by 5 points on a 0 to 100 scale. Table 15.5.c shows some illustrative results from this method. The risk differences can then be converted to NNTs or to people per thousand using methods described in Section 15.4.4 .

Table 15.5.c Risk difference derived for specific SMDs for various given ‘proportions improved’ in the comparator group (Furukawa 1999, Guyatt et al 2013b). Reproduced with permission of Elsevier 

15.5.3.4 Ratio of means

A more frequently used approach is based on calculation of a ratio of means between the intervention and comparator groups (Friedrich et al 2008) as discussed in Chapter 6, Section 6.5.1.3 . Interpretational advantages of this approach include the ability to pool studies with outcomes expressed in different units directly, to avoid the vulnerability of heterogeneous populations that limits approaches that rely on SD units, and for ease of clinical interpretation (row 2, Table 15.5.a and Table 15.5.b ). This method is currently designed for post-intervention scores only. However, it is possible to calculate a ratio of change scores if both intervention and comparator groups change in the same direction in each relevant study, and this ratio may sometimes be informative.

Limitations to this approach include its limited applicability to change scores (since it is unlikely that both intervention and comparator group changes are in the same direction in all studies) and the possibility of misleading results if the comparator group mean is very small, in which case even a modest difference from the intervention group will yield a large and therefore misleading ratio of means. It also requires that separate ratios of means be calculated for each included study, and then entered into a generic inverse variance meta-analysis (see Chapter 10, Section 10.3 ).

The ratio of means approach illustrated in Table 15.5.b suggests a relative reduction in pain of only 13%, meaning that those receiving steroids have a pain severity 87% of those in the comparator group, an effect that might be considered modest.

15.5.3.5 Presenting continuous results as minimally important difference units

To express results in MID units, review authors have two options. First, they can be combined across studies in the same way as the SMD, but instead of dividing the mean difference of each study by its SD, review authors divide by the MID associated with that outcome (Johnston et al 2010, Guyatt et al 2013b). Instead of SD units, the pooled results represent MID units (row 3, Table 15.5.a and Table 15.5.b ), and may be more easily interpretable. This approach avoids the problem of varying SDs across studies that may distort estimates of effect in approaches that rely on the SMD. The approach, however, relies on having well-established MIDs. The approach is also risky in that a difference less than the MID may be interpreted as trivial when a substantial proportion of patients may have achieved an important benefit.

The other approach makes a simple conversion (not shown in Table 15.5.b ), before undertaking the meta-analysis, of the means and SDs from each study to means and SDs on the scale of a particular familiar instrument whose MID is known. For example, one can rescale the mean and SD of other chronic respiratory disease instruments (e.g. rescaling a 0 to 100 score of an instrument) to a the 1 to 7 score in Chronic Respiratory Disease Questionnaire (CRQ) units (by assuming 0 equals 1 and 100 equals 7 on the CRQ). Given the MID of the CRQ of 0.5, a mean difference in change of 0.71 after rescaling of all studies suggests a substantial effect of the intervention (Guyatt et al 2013b). This approach, presenting in units of the most familiar instrument, may be the most desirable when the target audiences have extensive experience with that instrument, particularly if the MID is well established.

15.6 Drawing conclusions

15.6.1 conclusions sections of a cochrane review.

Authors’ conclusions in a Cochrane Review are divided into implications for practice and implications for research. While Cochrane Reviews about interventions can provide meaningful information and guidance for practice, decisions about the desirable and undesirable consequences of healthcare options require evidence and judgements for criteria that most Cochrane Reviews do not provide (Alonso-Coello et al 2016). In describing the implications for practice and the development of recommendations, however, review authors may consider the certainty of the evidence, the balance of benefits and harms, and assumed values and preferences.

15.6.2 Implications for practice

Drawing conclusions about the practical usefulness of an intervention entails making trade-offs, either implicitly or explicitly, between the estimated benefits, harms and the values and preferences. Making such trade-offs, and thus making specific recommendations for an action in a specific context, goes beyond a Cochrane Review and requires additional evidence and informed judgements that most Cochrane Reviews do not provide (Alonso-Coello et al 2016). Such judgements are typically the domain of clinical practice guideline developers for which Cochrane Reviews will provide crucial information (Graham et al 2011, Schünemann et al 2014, Zhang et al 2018a). Thus, authors of Cochrane Reviews should not make recommendations.

If review authors feel compelled to lay out actions that clinicians and patients could take, they should – after describing the certainty of evidence and the balance of benefits and harms – highlight different actions that might be consistent with particular patterns of values and preferences. Other factors that might influence a decision should also be highlighted, including any known factors that would be expected to modify the effects of the intervention, the baseline risk or status of the patient, costs and who bears those costs, and the availability of resources. Review authors should ensure they consider all patient-important outcomes, including those for which limited data may be available. In the context of public health reviews the focus may be on population-important outcomes as the target may be an entire (non-diseased) population and include outcomes that are not measured in the population receiving an intervention (e.g. a reduction of transmission of infections from those receiving an intervention). This process implies a high level of explicitness in judgements about values or preferences attached to different outcomes and the certainty of the related evidence (Zhang et al 2018b, Zhang et al 2018c); this and a full cost-effectiveness analysis is beyond the scope of most Cochrane Reviews (although they might well be used for such analyses; see Chapter 20 ).

A review on the use of anticoagulation in cancer patients to increase survival (Akl et al 2011a) provides an example for laying out clinical implications for situations where there are important trade-offs between desirable and undesirable effects of the intervention: “The decision for a patient with cancer to start heparin therapy for survival benefit should balance the benefits and downsides and integrate the patient’s values and preferences. Patients with a high preference for a potential survival prolongation, limited aversion to potential bleeding, and who do not consider heparin (both UFH or LMWH) therapy a burden may opt to use heparin, while those with aversion to bleeding may not.”

15.6.3 Implications for research

The second category for authors’ conclusions in a Cochrane Review is implications for research. To help people make well-informed decisions about future healthcare research, the ‘Implications for research’ section should comment on the need for further research, and the nature of the further research that would be most desirable. It is helpful to consider the population, intervention, comparison and outcomes that could be addressed, or addressed more effectively in the future, in the context of the certainty of the evidence in the current review (Brown et al 2006):

• P (Population): diagnosis, disease stage, comorbidity, risk factor, sex, age, ethnic group, specific inclusion or exclusion criteria, clinical setting;
• I (Intervention): type, frequency, dose, duration, prognostic factor;
• C (Comparison): placebo, routine care, alternative treatment/management;
• O (Outcome): which clinical or patient-related outcomes will the researcher need to measure, improve, influence or accomplish? Which methods of measurement should be used?

While Cochrane Review authors will find the PICO domains helpful, the domains of the GRADE certainty framework further support understanding and describing what additional research will improve the certainty in the available evidence. Note that as the certainty of the evidence is likely to vary by outcome, these implications will be specific to certain outcomes in the review. Table 15.6.a shows how review authors may be aided in their interpretation of the body of evidence and drawing conclusions about future research and practice.

Table 15.6.a Implications for research and practice suggested by individual GRADE domains

The review of compression stockings for prevention of deep vein thrombosis (DVT) in airline passengers described in Chapter 14 provides an example where there is some convincing evidence of a benefit of the intervention: “This review shows that the question of the effects on symptomless DVT of wearing versus not wearing compression stockings in the types of people studied in these trials should now be regarded as answered. Further research may be justified to investigate the relative effects of different strengths of stockings or of stockings compared to other preventative strategies. Further randomised trials to address the remaining uncertainty about the effects of wearing versus not wearing compression stockings on outcomes such as death, pulmonary embolism and symptomatic DVT would need to be large.” (Clarke et al 2016).

A review of therapeutic touch for anxiety disorder provides an example of the implications for research when no eligible studies had been found: “This review highlights the need for randomized controlled trials to evaluate the effectiveness of therapeutic touch in reducing anxiety symptoms in people diagnosed with anxiety disorders. Future trials need to be rigorous in design and delivery, with subsequent reporting to include high quality descriptions of all aspects of methodology to enable appraisal and interpretation of results.” (Robinson et al 2007).

15.6.4 Reaching conclusions

A common mistake is to confuse ‘no evidence of an effect’ with ‘evidence of no effect’. When the confidence intervals are too wide (e.g. including no effect), it is wrong to claim that the experimental intervention has ‘no effect’ or is ‘no different’ from the comparator intervention. Review authors may also incorrectly ‘positively’ frame results for some effects but not others. For example, when the effect estimate is positive for a beneficial outcome but confidence intervals are wide, review authors may describe the effect as promising. However, when the effect estimate is negative for an outcome that is considered harmful but the confidence intervals include no effect, review authors report no effect. Another mistake is to frame the conclusion in wishful terms. For example, review authors might write, “there were too few people in the analysis to detect a reduction in mortality” when the included studies showed a reduction or even increase in mortality that was not ‘statistically significant’. One way of avoiding errors such as these is to consider the results blinded; that is, consider how the results would be presented and framed in the conclusions if the direction of the results was reversed. If the confidence interval for the estimate of the difference in the effects of the interventions overlaps with no effect, the analysis is compatible with both a true beneficial effect and a true harmful effect. If one of the possibilities is mentioned in the conclusion, the other possibility should be mentioned as well. Table 15.6.b suggests narrative statements for drawing conclusions based on the effect estimate from the meta-analysis and the certainty of the evidence.

Table 15.6.b Suggested narrative statements for phrasing conclusions

Another common mistake is to reach conclusions that go beyond the evidence. Often this is done implicitly, without referring to the additional information or judgements that are used in reaching conclusions about the implications of a review for practice. Even when additional information and explicit judgements support conclusions about the implications of a review for practice, review authors rarely conduct systematic reviews of the additional information. Furthermore, implications for practice are often dependent on specific circumstances and values that must be taken into consideration. As we have noted, review authors should always be cautious when drawing conclusions about implications for practice and they should not make recommendations.

15.7 Chapter information

Authors: Holger J Schünemann, Gunn E Vist, Julian PT Higgins, Nancy Santesso, Jonathan J Deeks, Paul Glasziou, Elie Akl, Gordon H Guyatt; on behalf of the Cochrane GRADEing Methods Group

Acknowledgements: Andrew Oxman, Jonathan Sterne, Michael Borenstein and Rob Scholten contributed text to earlier versions of this chapter.

Funding: This work was in part supported by funding from the Michael G DeGroote Cochrane Canada Centre and the Ontario Ministry of Health. JJD receives support from the National Institute for Health Research (NIHR) Birmingham Biomedical Research Centre at the University Hospitals Birmingham NHS Foundation Trust and the University of Birmingham. JPTH receives support from the NIHR Biomedical Research Centre at University Hospitals Bristol NHS Foundation Trust and the University of Bristol. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.

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Santesso N, Carrasco-Labra A, Langendam M, Brignardello-Petersen R, Mustafa RA, Heus P, Lasserson T, Opiyo N, Kunnamo I, Sinclair D, Garner P, Treweek S, Tovey D, Akl EA, Tugwell P, Brozek JL, Guyatt G, Schünemann HJ. Improving GRADE evidence tables part 3: detailed guidance for explanatory footnotes supports creating and understanding GRADE certainty in the evidence judgments. Journal of Clinical Epidemiology 2016; 74 : 28-39.

Schünemann HJ, Puhan M, Goldstein R, Jaeschke R, Guyatt GH. Measurement properties and interpretability of the Chronic respiratory disease questionnaire (CRQ). COPD: Journal of Chronic Obstructive Pulmonary Disease 2005; 2 : 81-89.

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Schünemann HJ. Methodological idiosyncracies, frameworks and challenges of non-pharmaceutical and non-technical treatment interventions. Zeitschrift für Evidenz, Fortbildung und Qualität im Gesundheitswesen 2013; 107 : 214-220.

Schünemann HJ, Tugwell P, Reeves BC, Akl EA, Santesso N, Spencer FA, Shea B, Wells G, Helfand M. Non-randomized studies as a source of complementary, sequential or replacement evidence for randomized controlled trials in systematic reviews on the effects of interventions. Research Synthesis Methods 2013; 4 : 49-62.

Schünemann HJ, Wiercioch W, Etxeandia I, Falavigna M, Santesso N, Mustafa R, Ventresca M, Brignardello-Petersen R, Laisaar KT, Kowalski S, Baldeh T, Zhang Y, Raid U, Neumann I, Norris SL, Thornton J, Harbour R, Treweek S, Guyatt G, Alonso-Coello P, Reinap M, Brozek J, Oxman A, Akl EA. Guidelines 2.0: systematic development of a comprehensive checklist for a successful guideline enterprise. CMAJ: Canadian Medical Association Journal 2014; 186 : E123-142.

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Overview of the Scientific Method

13 Drawing Conclusions and Reporting the Results

Learning objectives.

• Identify the conclusions researchers can make based on the outcome of their studies.
• Describe why scientists avoid the term “scientific proof.”
• Explain the different ways that scientists share their findings.

Drawing Conclusions

Since statistics are probabilistic in nature and findings can reflect type I or type II errors, we cannot use the results of a single study to conclude with certainty that a theory is true. Rather theories are supported, refuted, or modified based on the results of research.

If the results are statistically significant and consistent with the hypothesis and the theory that was used to generate the hypothesis, then researchers can conclude that the theory is supported. Not only did the theory make an accurate prediction, but there is now a new phenomenon that the theory accounts for. If a hypothesis is disconfirmed in a systematic empirical study, then the theory has been weakened. It made an inaccurate prediction, and there is now a new phenomenon that it does not account for.

Although this seems straightforward, there are some complications. First, confirming a hypothesis can strengthen a theory but it can never prove a theory. In fact, scientists tend to avoid the word “prove” when talking and writing about theories. One reason for this avoidance is that the result may reflect a type I error.  Another reason for this  avoidance  is that there may be other plausible theories that imply the same hypothesis, which means that confirming the hypothesis strengthens all those theories equally. A third reason is that it is always possible that another test of the hypothesis or a test of a new hypothesis derived from the theory will be disconfirmed. This  difficulty  is a version of the famous philosophical “problem of induction.” One cannot definitively prove a general principle (e.g., “All swans are white.”) just by observing confirming cases (e.g., white swans)—no matter how many. It is always possible that a disconfirming case (e.g., a black swan) will eventually come along. For these reasons, scientists tend to think of theories—even highly successful ones—as subject to revision based on new and unexpected observations.

A second complication has to do with what it means when a hypothesis is disconfirmed. According to the strictest version of the hypothetico-deductive method, disconfirming a hypothesis disproves the theory it was derived from. In formal logic, the premises “if  A  then  B ” and “not  B ” necessarily lead to the conclusion “not  A .” If  A  is the theory and  B  is the hypothesis (“if  A  then  B ”), then disconfirming the hypothesis (“not  B ”) must mean that the theory is incorrect (“not  A ”). In practice, however, scientists do not give up on their theories so easily. One reason is that one disconfirmed hypothesis could be a missed opportunity (the result of a type II error) or it could be the result of a faulty research design. Perhaps the researcher did not successfully manipulate the independent variable or measure the dependent variable.

A disconfirmed hypothesis could also mean that some unstated but relatively minor assumption of the theory was not met. For example, if Zajonc had failed to find social facilitation in cockroaches, he could have concluded that drive theory is still correct but it applies only to animals with sufficiently complex nervous systems. That is, the evidence from a study can be used to modify a theory.  This practice does not mean that researchers are free to ignore disconfirmations of their theories. If they cannot improve their research designs or modify their theories to account for repeated disconfirmations, then they eventually must abandon their theories and replace them with ones that are more successful.

The bottom line here is that because statistics are probabilistic in nature and because all research studies have flaws there is no such thing as scientific proof, there is only scientific evidence.

Reporting the Results

The final step in the research process involves reporting the results. As described in the section on Reviewing the Research Literature in this chapter, results are typically reported in peer-reviewed journal articles and at conferences.

The most prestigious way to report one’s findings is by writing a manuscript and having it published in a peer-reviewed scientific journal. Manuscripts published in psychology journals typically must adhere to the writing style of the American Psychological Association (APA style). You will likely be learning the major elements of this writing style in this course.

Another way to report findings is by writing a book chapter that is published in an edited book. Preferably the editor of the book puts the chapter through peer review but this is not always the case and some scientists are invited by editors to write book chapters.

A fun way to disseminate findings is to give a presentation at a conference. This can either be done as an oral presentation or a poster presentation. Oral presentations involve getting up in front of an audience of fellow scientists and giving a talk that might last anywhere from 10 minutes to 1 hour (depending on the conference) and then fielding questions from the audience. Alternatively, poster presentations involve summarizing the study on a large poster that provides a brief overview of the purpose, methods, results, and discussion. The presenter stands by their poster for an hour or two and discusses it with people who pass by. Presenting one’s work at a conference is a great way to get feedback from one’s peers before attempting to undergo the more rigorous peer-review process involved in publishing a journal article.

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Research Paper Conclusion – Writing Guide and Examples

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Research Paper Conclusion

Definition:

A research paper conclusion is the final section of a research paper that summarizes the key findings, significance, and implications of the research. It is the writer’s opportunity to synthesize the information presented in the paper, draw conclusions, and make recommendations for future research or actions.

The conclusion should provide a clear and concise summary of the research paper, reiterating the research question or problem, the main results, and the significance of the findings. It should also discuss the limitations of the study and suggest areas for further research.

Parts of Research Paper Conclusion

The parts of a research paper conclusion typically include:

Restatement of the Thesis

The conclusion should begin by restating the thesis statement from the introduction in a different way. This helps to remind the reader of the main argument or purpose of the research.

Summary of Key Findings

The conclusion should summarize the main findings of the research, highlighting the most important results and conclusions. This section should be brief and to the point.

Implications and Significance

In this section, the researcher should explain the implications and significance of the research findings. This may include discussing the potential impact on the field or industry, highlighting new insights or knowledge gained, or pointing out areas for future research.

Limitations and Recommendations

It is important to acknowledge any limitations or weaknesses of the research and to make recommendations for how these could be addressed in future studies. This shows that the researcher is aware of the potential limitations of their work and is committed to improving the quality of research in their field.

Concluding Statement

The conclusion should end with a strong concluding statement that leaves a lasting impression on the reader. This could be a call to action, a recommendation for further research, or a final thought on the topic.

How to Write Research Paper Conclusion

Here are some steps you can follow to write an effective research paper conclusion:

• Restate the research problem or question: Begin by restating the research problem or question that you aimed to answer in your research. This will remind the reader of the purpose of your study.
• Summarize the main points: Summarize the key findings and results of your research. This can be done by highlighting the most important aspects of your research and the evidence that supports them.
• Discuss the implications: Discuss the implications of your findings for the research area and any potential applications of your research. You should also mention any limitations of your research that may affect the interpretation of your findings.
• Provide a conclusion : Provide a concise conclusion that summarizes the main points of your paper and emphasizes the significance of your research. This should be a strong and clear statement that leaves a lasting impression on the reader.
• Offer suggestions for future research: Lastly, offer suggestions for future research that could build on your findings and contribute to further advancements in the field.

Remember that the conclusion should be brief and to the point, while still effectively summarizing the key findings and implications of your research.

Example of Research Paper Conclusion

Here’s an example of a research paper conclusion:

Conclusion :

In conclusion, our study aimed to investigate the relationship between social media use and mental health among college students. Our findings suggest that there is a significant association between social media use and increased levels of anxiety and depression among college students. This highlights the need for increased awareness and education about the potential negative effects of social media use on mental health, particularly among college students.

Despite the limitations of our study, such as the small sample size and self-reported data, our findings have important implications for future research and practice. Future studies should aim to replicate our findings in larger, more diverse samples, and investigate the potential mechanisms underlying the association between social media use and mental health. In addition, interventions should be developed to promote healthy social media use among college students, such as mindfulness-based approaches and social media detox programs.

Overall, our study contributes to the growing body of research on the impact of social media on mental health, and highlights the importance of addressing this issue in the context of higher education. By raising awareness and promoting healthy social media use among college students, we can help to reduce the negative impact of social media on mental health and improve the well-being of young adults.

Purpose of Research Paper Conclusion

The purpose of a research paper conclusion is to provide a summary and synthesis of the key findings, significance, and implications of the research presented in the paper. The conclusion serves as the final opportunity for the writer to convey their message and leave a lasting impression on the reader.

The conclusion should restate the research problem or question, summarize the main results of the research, and explain their significance. It should also acknowledge the limitations of the study and suggest areas for future research or action.

Overall, the purpose of the conclusion is to provide a sense of closure to the research paper and to emphasize the importance of the research and its potential impact. It should leave the reader with a clear understanding of the main findings and why they matter. The conclusion serves as the writer’s opportunity to showcase their contribution to the field and to inspire further research and action.

When to Write Research Paper Conclusion

The conclusion of a research paper should be written after the body of the paper has been completed. It should not be written until the writer has thoroughly analyzed and interpreted their findings and has written a complete and cohesive discussion of the research.

Before writing the conclusion, the writer should review their research paper and consider the key points that they want to convey to the reader. They should also review the research question, hypotheses, and methodology to ensure that they have addressed all of the necessary components of the research.

Once the writer has a clear understanding of the main findings and their significance, they can begin writing the conclusion. The conclusion should be written in a clear and concise manner, and should reiterate the main points of the research while also providing insights and recommendations for future research or action.

Characteristics of Research Paper Conclusion

The characteristics of a research paper conclusion include:

• Clear and concise: The conclusion should be written in a clear and concise manner, summarizing the key findings and their significance.
• Comprehensive: The conclusion should address all of the main points of the research paper, including the research question or problem, the methodology, the main results, and their implications.
• Future-oriented : The conclusion should provide insights and recommendations for future research or action, based on the findings of the research.
• Impressive : The conclusion should leave a lasting impression on the reader, emphasizing the importance of the research and its potential impact.
• Objective : The conclusion should be based on the evidence presented in the research paper, and should avoid personal biases or opinions.
• Unique : The conclusion should be unique to the research paper and should not simply repeat information from the introduction or body of the paper.

Advantages of Research Paper Conclusion

The advantages of a research paper conclusion include:

• Summarizing the key findings : The conclusion provides a summary of the main findings of the research, making it easier for the reader to understand the key points of the study.
• Emphasizing the significance of the research: The conclusion emphasizes the importance of the research and its potential impact, making it more likely that readers will take the research seriously and consider its implications.
• Providing recommendations for future research or action : The conclusion suggests practical recommendations for future research or action, based on the findings of the study.
• Providing closure to the research paper : The conclusion provides a sense of closure to the research paper, tying together the different sections of the paper and leaving a lasting impression on the reader.
• Demonstrating the writer’s contribution to the field : The conclusion provides the writer with an opportunity to showcase their contribution to the field and to inspire further research and action.

Limitations of Research Paper Conclusion

While the conclusion of a research paper has many advantages, it also has some limitations that should be considered, including:

• I nability to address all aspects of the research: Due to the limited space available in the conclusion, it may not be possible to address all aspects of the research in detail.
• Subjectivity : While the conclusion should be objective, it may be influenced by the writer’s personal biases or opinions.
• Lack of new information: The conclusion should not introduce new information that has not been discussed in the body of the research paper.
• Lack of generalizability: The conclusions drawn from the research may not be applicable to other contexts or populations, limiting the generalizability of the study.
• Misinterpretation by the reader: The reader may misinterpret the conclusions drawn from the research, leading to a misunderstanding of the findings.

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Drawing Conclusions

For any research project and any scientific discipline, drawing conclusions is the final, and most important, part of the process.

This article is a part of the guide:

• Null Hypothesis
• Research Hypothesis
• Defining a Research Problem
• Selecting Method

Browse Full Outline

• 1 Scientific Method
• 2.1.1 Null Hypothesis
• 2.1.2 Research Hypothesis
• 2.2 Prediction
• 2.3 Conceptual Variable
• 3.1 Operationalization
• 3.2 Selecting Method
• 3.3 Measurements
• 3.4 Scientific Observation
• 4.1 Empirical Evidence
• 5.1 Generalization
• 5.2 Errors in Conclusion

Whichever reasoning processes and research methods were used, the final conclusion is critical, determining success or failure. If an otherwise excellent experiment is summarized by a weak conclusion, the results will not be taken seriously.

Success or failure is not a measure of whether a hypothesis is accepted or refuted, because both results still advance scientific knowledge.

Failure lies in poor experimental design, or flaws in the reasoning processes, which invalidate the results. As long as the research process is robust and well designed, then the findings are sound, and the process of drawing conclusions begins.

The key is to establish what the results mean. How are they applied to the world?

What Has Been Learned?

Generally, a researcher will summarize what they believe has been learned from the research, and will try to assess the strength of the hypothesis.

Even if the null hypothesis is accepted, a strong conclusion will analyze why the results were not as predicted. 

Theoretical physicist Wolfgang Pauli was known to have criticized another physicist’s work by saying, “it’s not only not right; it is not even wrong.”

While this is certainly a humorous put-down, it also points to the value of the null hypothesis in science, i.e. the value of being “wrong.” Both accepting or rejecting the null hypothesis provides useful information – it is only when the research provides no illumination on the phenomenon at all that it is truly a failure.

In observational research , with no hypothesis, the researcher will analyze the findings, and establish if any valuable new information has been uncovered. The conclusions from this type of research may well inspire the development of a new hypothesis for further experiments. 

Generating Leads for Future Research

However, very few experiments give clear-cut results, and most research uncovers more questions than answers.

The researcher can use these to suggest interesting directions for further study. If, for example, the null hypothesis was accepted, there may still have been trends apparent within the results. These could form the basis of further study, or experimental refinement and redesign.

Question: Let’s say a researcher is interested in whether people who are ambidextrous (can write with either hand) are more likely to have ADHD. She may have three groups – left-handed, right-handed and ambidextrous, and ask each of them to complete an ADHD screening.

She hypothesizes that the ambidextrous people will in fact be more prone to symptoms of ADHD. While she doesn’t find a significant difference when she compares the mean scores of the groups, she does notice another trend: the ambidextrous people seem to score lower overall on tests of verbal acuity. She accepts the null hypothesis, but wishes to continue with her research. Can you think of a direction her research could take, given what she has already learnt?

Answer: She may decide to look more closely at that trend. She may design another experiment to isolate the variable of verbal acuity, by controlling for everything else. This may eventually help her arrive at a new hypothesis: ambidextrous people have lower verbal acuity.

Evaluating Flaws in the Research Process

The researcher will then evaluate any apparent problems with the experiment. This involves critically evaluating any weaknesses and errors in the design, which may have influenced the results .

Even strict, ' true experimental ,' designs have to make compromises, and the researcher must be thorough in pointing these out, justifying the methodology and reasoning.

For example, when drawing conclusions, the researcher may think that another causal effect influenced the results, and that this variable was not eliminated during the experimental process . A refined version of the experiment may help to achieve better results, if the new effect is included in the design process.

In the global warming example, the researcher might establish that carbon dioxide emission alone cannot be responsible for global warming. They may decide that another effect is contributing, so propose that methane may also be a factor in global warming. A new study would incorporate methane into the model.

What are the Benefits of the Research?

The next stage is to evaluate the advantages and benefits of the research.

In medicine and psychology, for example, the results may throw out a new way of treating a medical problem, so the advantages are obvious.

In some fields, certain kinds of research may not typically be seen as beneficial, regardless of the results obtained. Ideally, researchers will consider the implications of their research beforehand, as well as any ethical considerations. In fields such as psychology, social sciences or sociology, it’s important to think about who the research serves and what will ultimately be done with the results.

For example, the study regarding ambidexterity and verbal acuity may be interesting, but what would be the effect of accepting that hypothesis? Would it really benefit anyone to know that the ambidextrous are less likely to have a high verbal acuity?

However, all well-constructed research is useful, even if it only strengthens or supports a more tentative conclusion made by prior research.

Suggestions Based Upon the Conclusions

The final stage is the researcher's recommendations based on the results, depending on the field of study. This area of the research process is informed by the researcher's judgement, and will integrate previous studies.

For example, a researcher interested in schizophrenia may recommend a more effective treatment based on what has been learnt from a study. A physicist might propose that our picture of the structure of the atom should be changed. A researcher could make suggestions for refinement of the experimental design, or highlight interesting areas for further study. This final piece of the paper is the most critical, and pulls together all of the findings into a coherent agrument.

The area in a research paper that causes intense and heated debate amongst scientists is often when drawing conclusions .

Sharing and presenting findings to the scientific community is a vital part of the scientific process. It is here that the researcher justifies the research, synthesizes the results and offers them up for scrutiny by their peers.

As the store of scientific knowledge increases and deepens, it is incumbent on researchers to work together. Long ago, a single scientist could discover and publish work that alone could have a profound impact on the course of history. Today, however, such impact can only be achieved in concert with fellow scientists.

Summary - The Strength of the Results

The key to drawing a valid conclusion is to ensure that the deductive and inductive processes are correctly used, and that all steps of the scientific method were followed.

Even the best-planned research can go awry, however. Part of interpreting results also includes the researchers putting aside their ego to appraise what, if anything went wrong. Has anything occurred to warrant a more cautious interpretation of results?

If your research had a robust design, questioning and scrutiny will be devoted to the experiment conclusion, rather than the methods.

Question: Researchers are interested in identifying new microbial species that are capable of breaking down cellulose for possible application in biofuel production. They collect soil samples from a particular forest and create laboratory cultures of every microbial species they discover there. They then “feed” each species a cellulose compound and observe that in all the species tested, there was no decrease in cellulose after 24 hours.

Read the following conclusions below and decide which of them is the most sound:

They conclude that there are no microbes that can break down cellulose.

They conclude that the sampled microbes are not capable of breaking down cellulose in a lab environment within 24 hours.

They conclude that all the species are related somehow.

They conclude that these microbes are not useful in the biofuel industry.

They conclude that microbes from forests don’t break down cellulose.

Answer: The most appropriate conclusion is number 2. As you can see, sound conclusions are often a question of not extrapolating too widely, or making assumptions that are not supported by the data obtained. Even conclusion number 2 will likely be presented as tentative, and only provides evidence given the limits of the methods used.

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How Do I Write the Conclusion?

Final Conclusions, Putting Your Work in Context and Considering Further Research

• First Online: 19 October 2023

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The conclusion is one of the shortest parts of the dissertation. In this chapter, we focus on the meaning and purpose of the conclusion, its components, and the sources of information that you should use to draw your conclusions. We will also point out the connection between the conclusion and the aim of the study, and things to avoid when writing the conclusion.

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Cottrell S (2017) Critical thinking skills: effective analysis, argument and reflection, 3rd edn. Palgrave, London

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McGregor SLT (2018) Understanding and evaluating research: a critical guide. SAGE Publications, Los Angeles, CA

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