Show that you understand the current state of research on your topic.
The length of a research proposal can vary quite a bit. A bachelor’s or master’s thesis proposal can be just a few pages, while proposals for PhD dissertations or research funding are usually much longer and more detailed. Your supervisor can help you determine the best length for your work.
One trick to get started is to think of your proposal’s structure as a shorter version of your thesis or dissertation , only without the results , conclusion and discussion sections.
Download our research proposal template
Discover proofreading & editing
Writing a research proposal can be quite challenging, but a good starting point could be to look at some examples. We’ve included a few for you below.
Like your dissertation or thesis, the proposal will usually have a title page that includes:
The first part of your proposal is the initial pitch for your project. Make sure it succinctly explains what you want to do and why.
Your introduction should:
To guide your introduction , include information about:
As you get started, it’s important to demonstrate that you’re familiar with the most important research on your topic. A strong literature review shows your reader that your project has a solid foundation in existing knowledge or theory. It also shows that you’re not simply repeating what other people have already done or said, but rather using existing research as a jumping-off point for your own.
In this section, share exactly how your project will contribute to ongoing conversations in the field by:
Following the literature review, restate your main objectives . This brings the focus back to your own project. Next, your research design or methodology section will describe your overall approach, and the practical steps you will take to answer your research questions.
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To finish your proposal on a strong note, explore the potential implications of your research for your field. Emphasize again what you aim to contribute and why it matters.
For example, your results might have implications for:
Last but not least, your research proposal must include correct citations for every source you have used, compiled in a reference list . To create citations quickly and easily, you can use our free APA citation generator .
Some institutions or funders require a detailed timeline of the project, asking you to forecast what you will do at each stage and how long it may take. While not always required, be sure to check the requirements of your project.
Here’s an example schedule to help you get started. You can also download a template at the button below.
Download our research schedule template
Research phase | Objectives | Deadline |
---|---|---|
1. Background research and literature review | 20th January | |
2. Research design planning | and data analysis methods | 13th February |
3. Data collection and preparation | with selected participants and code interviews | 24th March |
4. Data analysis | of interview transcripts | 22nd April |
5. Writing | 17th June | |
6. Revision | final work | 28th July |
If you are applying for research funding, chances are you will have to include a detailed budget. This shows your estimates of how much each part of your project will cost.
Make sure to check what type of costs the funding body will agree to cover. For each item, include:
To determine your budget, think about:
If you want to know more about the research process , methodology , research bias , or statistics , make sure to check out some of our other articles with explanations and examples.
Methodology
Statistics
Research bias
Once you’ve decided on your research objectives , you need to explain them in your paper, at the end of your problem statement .
Keep your research objectives clear and concise, and use appropriate verbs to accurately convey the work that you will carry out for each one.
I will compare …
A research aim is a broad statement indicating the general purpose of your research project. It should appear in your introduction at the end of your problem statement , before your research objectives.
Research objectives are more specific than your research aim. They indicate the specific ways you’ll address the overarching aim.
A PhD, which is short for philosophiae doctor (doctor of philosophy in Latin), is the highest university degree that can be obtained. In a PhD, students spend 3–5 years writing a dissertation , which aims to make a significant, original contribution to current knowledge.
A PhD is intended to prepare students for a career as a researcher, whether that be in academia, the public sector, or the private sector.
A master’s is a 1- or 2-year graduate degree that can prepare you for a variety of careers.
All master’s involve graduate-level coursework. Some are research-intensive and intend to prepare students for further study in a PhD; these usually require their students to write a master’s thesis . Others focus on professional training for a specific career.
Critical thinking refers to the ability to evaluate information and to be aware of biases or assumptions, including your own.
Like information literacy , it involves evaluating arguments, identifying and solving problems in an objective and systematic way, and clearly communicating your ideas.
The best way to remember the difference between a research plan and a research proposal is that they have fundamentally different audiences. A research plan helps you, the researcher, organize your thoughts. On the other hand, a dissertation proposal or research proposal aims to convince others (e.g., a supervisor, a funding body, or a dissertation committee) that your research topic is relevant and worthy of being conducted.
If you want to cite this source, you can copy and paste the citation or click the “Cite this Scribbr article” button to automatically add the citation to our free Citation Generator.
McCombes, S. & George, T. (2023, November 21). How to Write a Research Proposal | Examples & Templates. Scribbr. Retrieved June 18, 2024, from https://www.scribbr.com/research-process/research-proposal/
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Home » Research Proposal – Types, Template and Example
Table of Contents
Research proposal is a document that outlines a proposed research project . It is typically written by researchers, scholars, or students who intend to conduct research to address a specific research question or problem.
Research proposals can vary depending on the nature of the research project and the specific requirements of the funding agency, academic institution, or research program. Here are some common types of research proposals:
This is the most common type of research proposal, which is prepared by students, scholars, or researchers to seek approval and funding for an academic research project. It includes all the essential components mentioned earlier, such as the introduction, literature review , methodology , and expected outcomes.
A grant proposal is specifically designed to secure funding from external sources, such as government agencies, foundations, or private organizations. It typically includes additional sections, such as a detailed budget, project timeline, evaluation plan, and a description of the project’s alignment with the funding agency’s priorities and objectives.
Students pursuing a master’s or doctoral degree often need to submit a proposal outlining their intended research for their dissertation or thesis. These proposals are usually more extensive and comprehensive, including an in-depth literature review, theoretical framework, research questions or hypotheses, and a detailed methodology.
This type of proposal is often prepared by researchers or research teams within an organization or institution. It outlines a specific research project that aims to address a particular problem, explore a specific area of interest, or provide insights for decision-making. Research project proposals may include sections on project management, collaboration, and dissemination of results.
Researchers or scholars applying for research fellowships may be required to submit a proposal outlining their proposed research project. These proposals often emphasize the novelty and significance of the research and its alignment with the goals and objectives of the fellowship program.
In cases where researchers from multiple institutions or disciplines collaborate on a research project, a collaborative research proposal is prepared. This proposal highlights the objectives, responsibilities, and contributions of each collaborator, as well as the overall research plan and coordination mechanisms.
A research proposal typically follows a standard outline that helps structure the document and ensure all essential components are included. While the specific headings and subheadings may vary slightly depending on the requirements of your institution or funding agency, the following outline provides a general structure for a research proposal:
———————————————————————————————–
Here’s an example of a research proposal to give you an idea of how it can be structured:
Title: The Impact of Social Media on Adolescent Well-being: A Mixed-Methods Study
This research proposal aims to investigate the impact of social media on the well-being of adolescents. The study will employ a mixed-methods approach, combining quantitative surveys and qualitative interviews to gather comprehensive data. The research objectives include examining the relationship between social media use and mental health, exploring the role of peer influence in shaping online behaviors, and identifying strategies for promoting healthy social media use among adolescents. The findings of this study will contribute to the understanding of the effects of social media on adolescent well-being and inform the development of targeted interventions.
1. Introduction
1.1 Background and Context:
Adolescents today are immersed in social media platforms, which have become integral to their daily lives. However, concerns have been raised about the potential negative impact of social media on their well-being, including increased rates of depression, anxiety, and body dissatisfaction. It is crucial to investigate this phenomenon further and understand the underlying mechanisms to develop effective strategies for promoting healthy social media use among adolescents.
1.2 Research Objectives:
The main objectives of this study are:
2. Literature Review
Extensive research has been conducted on the impact of social media on adolescents. Existing literature suggests that excessive social media use can contribute to negative outcomes, such as low self-esteem, cyberbullying, and addictive behaviors. However, some studies have also highlighted the positive aspects of social media, such as providing opportunities for self-expression and social support. This study will build upon this literature by incorporating both quantitative and qualitative approaches to gain a more nuanced understanding of the relationship between social media and adolescent well-being.
3. Methodology
3.1 Research Design:
This study will adopt a mixed-methods approach, combining quantitative surveys and qualitative interviews. The quantitative phase will involve administering standardized questionnaires to a representative sample of adolescents to assess their social media use, mental health indicators, and perceived social support. The qualitative phase will include in-depth interviews with a subset of participants to explore their experiences, motivations, and perceptions related to social media use.
3.2 Data Collection Methods:
Quantitative data will be collected through an online survey distributed to schools in the target region. The survey will include validated scales to measure social media use, mental health outcomes, and perceived social support. Qualitative data will be collected through semi-structured interviews with a purposive sample of participants. The interviews will be audio-recorded and transcribed for thematic analysis.
3.3 Data Analysis:
Quantitative data will be analyzed using descriptive statistics and regression analysis to examine the relationships between variables. Qualitative data will be analyzed thematically to identify common themes and patterns within participants’ narratives. Integration of quantitative and qualitative findings will provide a comprehensive understanding of the research questions.
4. Timeline
The research project will be conducted over a period of 12 months, divided into specific phases, including literature review, study design, data collection, analysis, and report writing. A detailed timeline outlining the key milestones and activities is provided in Appendix A.
5. Expected Outcomes and Significance
This study aims to contribute to the existing literature on the impact of social media on adolescent well-being by employing a mixed-methods approach. The findings will inform the development of evidence-based interventions and guidelines to promote healthy social media use among adolescents. This research has the potential to benefit adolescents, parents, educators, and policymakers by providing insights into the complex relationship between social media and well-being and offering strategies for fostering positive online experiences.
6. Resources
The resources required for this research include access to a representative sample of adolescents, research assistants for data collection, statistical software for data analysis, and funding to cover survey administration and participant incentives. Ethical considerations will be taken into account, ensuring participant confidentiality and obtaining informed consent.
7. References
Writing a research proposal can be a complex task, but with proper guidance and organization, you can create a compelling and well-structured proposal. Here’s a step-by-step guide to help you through the process:
The length of a research proposal can vary depending on the specific guidelines provided by your institution or funding agency. However, research proposals typically range from 1,500 to 3,000 words, excluding references and any additional supporting documents.
The purpose of a research proposal is to outline and communicate your research project to others, such as academic institutions, funding agencies, or potential collaborators. It serves several important purposes:
The research proposal holds significant importance in the research process. Here are some key reasons why research proposals are important:
The timing of when to write a research proposal can vary depending on the specific requirements and circumstances. However, here are a few common situations when it is appropriate to write a research proposal:
Researcher, Academic Writer, Web developer
Bad management habits, even if they are small, are amplified in hybrid work.
Hybrid work is here to stay, and while many organizations are deciding how many days a week people can be remote and protocols for Microsoft Teams calls, they are forgetting to train staff on what human interactions should look like.
As a result, workers describe a "perceived frenzy." Meetings are canceled without clear explanations. Managers are multi-tasking during calls, and workers detect that they are distracted.
While these are certainly not malicious acts, they create a "heads down, get your work done" culture where workers are at best hesitant and at worst afraid to express concerns, questions and ideas. In other words, there is less "psychological safety" for workers, according to research conducted last year by Peggy Kendall, professor of communication studies, and Triston Thomas, a student, at Bethel University in Arden Hills.
The research started after surveys showed managers saw less creativity from their teams when workers were remote.
More than 36 million employees will work remotely by 2025, according to research. While most love it, nearly a quarter of managers find their teams are less creative when they work from home.
In Minnesota, the Federal Reserve estimates one-third of workers are remote at least part-time. Other surveys show workers would quit if forced to work in the office 100% of the time.
So managers need to figure out how to make the arrangement work.
Blue Cross and Blue Shield of Minnesota, ranked 34th on the Star Tribune's Top Workplaces list of large companies, has shifted the culture of achievement to be outcome-based instead of activity-based.
"You have to be very intentional when you have a remote workforce to understand what they need to deliver and being clear and setting expectations with that," said Lisa Kramer Rodacker, senior director of organization development and enterprise learning. "You're really focusing on: What do I expect out of them in terms of those outcomes and then holding individuals accountable to that. And that's a mindset shift, for some of our leaders."
Before the pandemic, 20% of BlueCross workers were fully remote. Now, two-thirds of the workforce is.
That reality means the organization's commitment to flexibility requires managers to know their employees on a deeper level, Kramer Rodacker said.
"What may work for somebody who's twenty-something is different than somebody who has little kids and something different maybe than empty nesters," Kramer Rodacker said.
That type of relationship needs to be built, said Kendall, who suggests managers make time during one-on-one meetings to ask about employees' well-being and build that relationship.
If you need to cancel the meeting, give a clear reason why and be fully present during it, she said. That means no background work or checking messages.
"If you're going to be an online manager, you have to give your employees enough information and check in often enough that they're not making up their own stories, like, 'My manager is too busy for me,' or, 'Nobody else really cares. I've got to figure this out on my own.' You have to interrupt the story," Kendall said.
To fully engage virtual participants in a meeting and show them their ideas are important, BlueCross teaches leaders to let those who are hybrid go first. Everyone also must have cameras on, so everyone's faces are seen, Kramer Rodacker said.
"If you're not actively including, you could be accidentally excluding," she said. "You can have a tendency of kind of 'out of sight, out of mind.' You've got to be really purposeful and intentional about making sure that you're engaging remote employees."
"Over-communicating" also can counter misperceptions, Kendall said. "Let's not assume that everything is OK."
In a physical workplace, employees can see when a manager or co-worker is intensely concentrating or busy, so during a lull, they can ask a process question.
But workers in the Bethel study said they were worried about seeming unprofessional, rude or disrespectful by expressing concerns through on-screen messaging because they didn't know their co-workers well, Thomas said during a presentation of the research at Bethel.
This meant that, at times, they went online to try to figure something out instead of asking a colleague. This resulted in a feeling of loneliness and being disconnected, he said.
So being intentional about communicating expectations and feedback on work, and asking regularly if workers need help or have questions can add to workers' comfort levels, Kendall said. Trust is essential in any work, but especially in a remote relationship.
"It takes longer to build; it has to be more intentional [with remote employees]," Kendall said. "It's going to take longer to build, and it can be destroyed much faster online as well."
About 30% of Field Nation's workers are remote, up from 10% before the pandemic.
Engagement scores at the company for remote U.S. employees were "very positive," which Teri Calderon, executive vice president for people and marketplace operations, attributes to a long-established corporate culture where cross-functional team members work together to solve problems.
Field Nation, which was 21st among midsize companies on the Top Workplaces list, brings all its U.S.-based workers to its Minneapolis corporate office twice a year for "Field Week." The event combines in-person learning and community building, which Calderon said is another important part of the culture for the company that matches information technology workers with companies.
The company also stresses regular one-on-one meetings with managers and remote employees and hybrid team meetings and town halls.
Field Nation also is intentional about helping employees build their internal networks, starting during the onboarding process. New employees are given a list of workers they should meet, Calderon said.
Another lesson: Training works better when employees in a session are all on site or all virtual, she said.
"Doing hybrid learning is really difficult because somebody feels left out of a conversation," Calderon said.
Employees also must feel connected to their employer's mission, said Dan Schiappa, chief product and services officer at Arctic Wolf, a cybersecurity firm based in Eden Prairie that ranks 11th among large companies on this year's Top Workplaces list.
"Great companies are built around employees who are empowered to take ownership of their individual mission, not just clock in for a paycheck," Schiappa wrote in an email. "That means granting all employees, especially those who are remote, the opportunity to speak their mind, share new ideas and influence those around them, regardless of their job title."
Strong leadership from managers is the only way to achieve that goal, though, Kendall said. Over-communicating and non-distracted talks are good techniques no matter who you manage but are key with remote workers.
"You have to be intentional about community," Kendall said.
Todd Nelson is a freelance writer in Lake Elmo. His email is [email protected] .
Politician who pushed philippines natural gas boom is behind firm that planned to profit, california workplace safety board approves heat protections for indoor workers, excluding prisons, how nvidia became an ai giant, federal officials are investigating a southwest airlines low flight over oklahoma city suburbs.
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Home > Conferences > AMCIS > AMCIS 2024 Proceedings > IS in Educ, IS Curriculum, and Teaching Cases (SIG ED) > 12
Proposal - Security Certifications, Degrees, & Work Experience: Which is better?
Garry White , Texas State Univeristy Follow
In this document we describe the formatting requirements for the Proceedings of the AMCIS Conference. Please review this document carefully. You can use this document as a template and copy/paste your paper content here (this might be the best or easiest way). Please be sure to adhere to the formatting requirements as this will be your camera-ready version, and a PDF format will be generated directly from your submitted final Word version. Please note several limitations on length: (1) your abstract should be no more than 150 words, as the abstract will also be used for the conference program, (2) your completed research paper should be no more than 10 pages (approx. 5,000 words, including figures, tables, references, and appendices). Emergent Research Forum papers are limited to 5 pages (approx. 2,500 words, including figures, tables, references, and appendices.) This paper length is intended to encourage authors to publish full-length papers in journals or other outlets later.
Recommended citation.
White, Garry, "Proposal - Security Certifications, Degrees, & Work Experience: Which is better?" (2024). AMCIS 2024 Proceedings . 12. https://aisel.aisnet.org/amcis2024/is_education/is_education/12
Since June 13, 2024
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Today, the U.S. National Science Foundation, in partnership with the American Association of Community Colleges (AACC), announced the three winning teams of the 2024 Community College Innovation Challenge (CCIC) .
The annual competition seeks to strengthen entrepreneurial thinking among community college students by challenging them to develop STEM-based solutions to real-world problems. It also enables students to discover and demonstrate their ability to translate knowledge into action and initiate real-world change.
"Year after year, I am thrilled to witness the promising talent that the Community College Innovation Challenge brings together," said James L. Moore III, assistant director for STEM Education. "The student participants represent both the present and future of STEM by addressing some of the most pressing challenges of our times. NSF is proud to co-sponsor CCIC and to congratulate the students for doing an outstanding job translating their knowledge into action."
The first, second and third-place winning teams and their innovations are listed below.
First Place Winner Perimeter College at Georgia State University, Georgia: The Perimeter College team seeks to redesign cervical cancer screening by offering a noninvasive alternative to the speculum. By making screening more accessible, this alternative has the potential to impact cervical cancer mortality rates, especially in low-income countries.
Second Place Winner Dallas College, Texas: Autonomous Monitoring for Blaze Emergency Response (AMBER) is an early detection system that uses infrared cameras and sensors to alert farmers and local authorities to fire risks. With a third-party drone provider, AMBER can quickly track and mobilize a rapid-fire response and preserve agricultural land.
Third Place Winner County College of Morris, New Jersey: The County College of Morris team proposes to safely and efficiently increase the world's energy supply through a molecular solar thermal system. This system is nontoxic, cost-efficient and can capture light energy as heat, converting stored heat into usable energy.
This week, 12 community colleges selected as finalists in a national competition attended an innovation boot camp, where they learned from entrepreneurs and experts in business planning, stakeholder engagement, strategic communication and marketplace dynamics. The boot camp culminated in a student poster session with STEM leaders and congressional stakeholders and a 5-minute pitch presentation to a panel of industry and entrepreneurial professionals determining the winning teams.
"Truly inspiring," said Walter G. Bumphus, president and CEO of AACC. "We are so proud to be afforded the opportunity to provide these resources for community college students to showcase their innovative and creative solutions to real-world issues. The projects featured show the amazing potential these students have to make meaningful economic and societal impact. Congratulations to the team from Georgia Perimeter College at Georgia State University and to all of the finalists."
This year, the 12 finalist teams presented solutions that addressed clean water, renewable energy and energy storage, HIV treatment, women's health care, fire prevention, combating plastic waste, and accessibility for people with disabilities.
8 common (and costly) mistakes to avoid 🤦.
By: Derek Jansen (MBA) & David Phair (PhD) . Reviewed By: Dr Eunice Rautenbach | June 2021
At Grad Coach, we review a lot of research proposals , including dissertation proposals and thesis proposals. Some are pretty good, while others are, well, not fantastic. Sadly, many students only approach us after their proposal has been rejected , meaning they’ve wasted a lot of time and effort.
We’ll look at 8 common mistakes and issues we see cropping up in research proposals so that you can craft your proposal with confidence and maximise the chances of it being approved.
One of the most common issues we see in dissertation and thesis proposals is that the research topic is simply too broad . In other words, the focus of the research is not ringfenced tightly enough (or just not defined clearly enough), resulting in a proposal that has an unclear direction or attempts to take on too much.
For example, a research project that aims to “investigate trust in the workplace” would be considered very broad. This topic has no specific focus and leaves many questions unanswered, for example:
As a general rule of thumb, you should aim for a fairly narrow focus when you craft your research topic. Doing this will allow you to go deep and investigate the topic in-depth , which is what the markers want to see. Quality beats quantity – or rather, depth beats breadth – when it comes to defining and refining your research topic.
A related problem is that oftentimes, students have a more refined topic within their mind, but they don’t articulate it well in their proposal. This often results in the proposal being rejected because the topic is perceived as being too broad. In other words, it’s important to ensure you not only have a clear, sharp focus for your research, but that you communicate that well in your dissertation or thesis proposal. Make sure that you address the who , what , were and when, so that your topic is well defined.
Let’s look at an example.
Sticking with the topic I mentioned earlier, a more refined and well-articulated research aim could be something along the lines of:
“To investigate the factors that cultivate organisational trust (i.e. a customer trusting an organisation) within the UK life insurance industry.”
As you can see, this is a lot more specific and ringfences the topic into a more manageable scope . So, when it comes to your research topic, remember to keep it tight .
Another common issue that we see with weaker research proposals is misalignment between the research aims and objectives , as well as with the research questions . Sometimes all three are misaligned , and sometimes there’s only one misfit. Whatever the case, it’s a problem that can lead to proposal rejection, as these three elements need to link together tightly.
Let’s look at an example of a misaligned trio.
Research Aim:
To identify factors that cultivate organisational trust in British insurance brokers.
Research Objectives:
To measure organisational trust levels across different demographic groups within the UK.
To investigate the causes of differences in organisational trust levels between groups.
Research Question:
What factors influence organisational trust between customers and insurance brokers within the UK?
As you can see, the research aim and research question are reasonably aligned (they are both focused on the factors that cultivate trust). However, the research objectives are misaligned, as they focus on measuring trust levels across different groups, rather than identifying what factors stimulate trust. This will result in a study that’s pulling in different directions – not good.
A related issue we see is that students don’t really understand the difference between research aims (the broader goal), research objectives (how you’ll achieve that goal) and research questions (the specific questions you’ll answer within your study). So, when you’re preparing your proposal, make sure that you clearly understand how these differ and make sure they’re all tightly aligned with each other.
A good research topic – in other words, a good set of research aims, research objectives and research questions – needs to be well justified to convince your university to approve your research. Poor justification of the research topic is a common reason for proposals to be rejected.
So, how do you justify your research?
For a research topic to be well justified, you need to demonstrate both originality and importance .
Originality means that your proposed research is novel , or at least that it’s novel within its context (for example, within a specific country or industry). While the extent of this novelty will vary depending on your institution, programme and level of study (e.g. Masters vs Doctorate), your research will always need to have some level of originality. In other words, you can’t research something that’s been researched ad nauseam before.
Simply put, your research needs to emerge from a gap in the existing literature . To do this, you need to figure out what’s missing from the current body of knowledge (by undertaking a review of the literature) and carve out your own research to fill that gap. We explain this process in more detail here .
Importance is the second factor. Just because a topic is unique doesn’t mean it’s important . You need to be able to explain what the benefits of undertaking your proposed research would be. Who would benefit? How would they benefit? How could the newly developed knowledge be used in the world, whether in academia or industry?
So, when you’re writing up your research proposal, make sure that you clearly articulate both the originality and importance of your proposed research, or you’ll risk submitting an unconvincing proposal.
As I mentioned in the previous point, your research topic needs to emerge from the existing research . In other words, your research needs to fill a clear gap in the literature – something that hasn’t been adequately researched, or that lacks research in a specific context.
To convince your university that your topic will fill a gap in the research, your proposal needs to have a strong theoretical foundation . In other words, you need to show that you’ve done the necessary reading and are familiar with the existing research. To do this, you need to provide an integrated summary of the existing research and highlight (very clearly) the theoretical gap that exists.
Some common signs of a weak theoretical foundation that we’ve encountered include:
While it’s generally not expected that you undertake a comprehensive literature review at the proposal stage, you do still need to justify your topic by demonstrating a need for your study (i.e. the literature gap). So, make sure that you put in the time to develop a sound understanding of the current state of knowledge in your space, and make sure that you communicate that understanding in your proposal by building your topic justification on a solid base of credible literature.
Once you’ve made a strong argument regarding the value of your research (i.e., you’ve justified it), the next matter that your research proposal needs to address is the “how” – in other words, your intended research design and methodology .
A common issue we see is that students don’t provide enough detail in this section. This is often because they don’t really know exactly what they’re going to do and plan to just “figure it out later” (which is not good enough). But sometimes it’s just a case of poor articulation – in other words, they have a clear design worked out in their minds, but they haven’t put their plan to paper.
Whatever the reason, a dissertation or thesis proposal that lacks detail regarding the research design runs a major risk of being rejected. This is because universities want to see that you have a clearly defined, practical plan to achieve your research aims and objectives and answer your research questions.
At a minimum, you should provide detail regarding the following:
For more information about each of these design decisions, check out our post detailing the Research Onion.
Of course, your research design can (and most likely will) evolve along the way , but you still need a starting point. Also, your proposed research design needs to be practical, given your constraints. A brilliant design is pointless if you don’t have the resources (e.g. money, equipment, expertise, etc.) to pull it off. So, get detailed in this section of your proposal and keep it realistic to maximise your chances of approval.
As with any document, poor writing and sloppy presentation can heavily detract from your research proposal, even if you tick all the other boxes. While poor writing and presentation alone probably won’t result in your proposal being rejected, it will definitely put you at a disadvantage , as it gives a negative impression regarding the overall quality of your work.
The main issues we see here are:
The good news is that many of these can be resolved by editing and proofreading your proposal beforehand, so it’s always a good idea to take the time to do this. It’s also a good idea to ask a friend to review your document, as you will invariably suffer from blindspots when editing your own work. If your budget allows, having your work reviewed by an academic editor will ensure you cover all bases and submit a high-quality document.
While different universities will have varying requirements, there is usually a requirement (or at least an expectation) for a project plan of sorts. As I mentioned earlier, a strong research proposal needs to be practical and manageable, given your constraints. Therefore, a well-articulated project plan that considers all the practicalities (and risks) is an important part of a strong research proposal.
We generally recommend that students draw up a fairly detailed Gantt chart , detailing each major task involved in the dissertation writing process. For example, you can break it down into the various chapters ( introduction , literature review, etc.) and the key tasks involved in completing each chapter (research, planning, writing, etc). What’s most important here is to be realistic – things almost always take longer than you expect, especially if you’re a first-time researcher.
We also recommend including some sort of risk management plan . For this, you could make use of a basic risk register , listing all the potential risks you foresee, as well as your mitigation and response actions, should they occur. For example, the risk of data collection taking longer than anticipated, the risk of not getting enough survey responses , etc.
What’s most important is to demonstrate that you have thought your research through and have a clear plan of action . Of course, as with your research design, plans can (and likely will) change – and that’s okay. However, you still need to have an initial plan, and that plan needs to be realistic and manageable, or you’ll risk your proposal getting rejected.
While research proposals are fairly generic in terms of contents and style, and tend to follow a reasonably standardised structure, each university has its nuances in terms of what they want to be included in the dissertation or thesis proposal.
Some universities want more or less detail in certain sections, some want extra sections, and some want a very specific structure and format (down to the font type and size!). So, you need to pay very close attention to whatever institution-specific criteria your university has set out.
Typically, your university will provide some sort of brief or guidance document to direct your proposal efforts, so be sure to study this document thoroughly and ask the faculty for clarity if you’re uncertain about anything. Some universities will also provide a proposal template . Pay careful attention to any specific structure they recommend as well as formatting requirements (such as font, line spacing, margin sizes, referencing format, etc.).
If your university provides an assessment criteria matrix , you’ve hit the jackpot, as that document will detail exactly what you need to achieve in each section of the proposal. Study that matrix inside out and make sure that your research proposal tightly aligns with the assessment criteria.
We’ve covered a lot here – let’s recap on the 8 common mistakes that can hurt your research proposal or even get it rejected:
If you have any questions about these common mistakes, leave a comment below and we’ll do our best to answer. You may also want to have a look at some examples of successful proposals here . If you’d like to get 1-on-1 help with your research proposal , book a free initial consultation with a friendly coach to discuss how we can move you forward.
This post is an extract from our bestselling short course, Research Proposal Bootcamp . If you want to work smart, you don't want to miss this .
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FDA regulates sunscreens, which are nonprescription drugs, to help make sure that consumers have access to safe and effective sun protection products. There have been several developments involving sunscreen regulation in the past few years. Today, there are two more: FDA is posting the deemed final order for over-the-counter (OTC) sunscreens and is issuing a proposed order for sunscreens.
In this CDER Conversation, Theresa Michele, M.D., director of the Office of Nonprescription Drugs, explains today’s activities and what the orders mean for consumers, health care providers, industry, and other stakeholders.
Sunscreens have been regulated by FDA since the 1970s, but they have garnered a lot of attention recently. In 2019, FDA issued a proposed rule on sunscreens , which proposed to revise the requirements for sunscreen active ingredients; maximum sun protection factor (SPF) levels ; broad spectrum requirements (protection against both ultraviolet A and B rays); and dosage forms (for example, cream, lotion, or spray), among other things. The proposed rule also included updates on how sunscreens are labeled to make it easier for consumers to identify key information.
The 2019 proposal aimed to bring sunscreens up to date with the latest science, including new information showing that certain sunscreen ingredients can be absorbed through the skin into the body. For more information on this issue, I co-authored two FDA Voices articles, one in 2019 and an update in 2020 , explaining sunscreen absorption studies.
Then came the 2020 Coronavirus Aid, Relief, and Economic Security Act, also known as the CARES Act , which Congress enacted in March 2020 in response to COVID-19. Most of its provisions focus on economic relief to individuals, families, businesses, and other groups. However, the CARES Act also reformed and modernized the way FDA regulates certain OTC monograph drugs, including sunscreen. As background, an OTC monograph is a “rule book” for each therapeutic category that establishes conditions, such as active ingredients, uses (indications), doses, labeling, and testing, under which an OTC drug is “generally recognized as safe and effective” (“GRASE” for short) and can be marketed without a new drug application and FDA pre-market approval.
The CARES Act replaced the rulemaking process for OTC monograph drugs with an administrative order process for issuing, revising, and amending the OTC monographs. The administrative order process gives FDA new tools to help revise the OTC monographs as science changes, innovation progresses, new data become available, or emerging safety signals arise.
In addition, the CARES Act established deemed final orders for certain OTC monograph therapeutic categories, which became effective in March 2020. The deemed final orders establish a baseline of current GRASE conditions for the therapeutic categories. To learn more about OTC monograph reform, please see this FDA Voices article I wrote in 2020 on the topic.
For sunscreens specifically, in addition to establishing a deemed final order, the CARES Act requires FDA to issue a proposed order to amend and revise the deemed final order for sunscreens.
It is important to remember that the proposed order is a proposal, and any new sunscreen requirements will not take effect until after the agency issues a final order. A 45-day public comment period began when FDA issued the proposed order. After reviewing and considering the comments, FDA will issue a final order with an effective date, which, by law, will not be earlier than one year after the agency issues the final order.
The requirements of the sunscreen deemed final order essentially keep the status quo.
The deemed final order for sunscreens includes certain requirements about active ingredients from the 1999 final monograph regulation for OTC sunscreen products , which never took effect, and the labeling and effectiveness requirements from a final 2011 labeling and effectiveness testing rule .
In addition to incorporating requirements already in effect under the final 2011 regulation, the deemed final order largely corresponds to the approach of an FDA sunscreen enforcement policy guidance, which had been in place before the CARES Act because the sunscreen monograph was not in effect.
Meanwhile, the proposed order proposes changes to these requirements to bring them up to date with the current science. When finalized, the proposed order will fully replace the deemed final order with new requirements for sunscreens.
FDA first articulated its proposed changes to the sunscreen OTC monograph in the 2019 proposed rule. We are now using this proposed order to efficiently transition our ongoing consideration of the appropriate requirements for OTC sunscreens from the previous rulemaking process to the new order process that the CARES Act created.
The CARES Act did not change the scientific standard for making a GRASE determination. For that reason, the proposed requirements in the proposed order are substantively the same as those in the 2019 proposed rule.
There are notable differences between the sunscreen deemed final order and the proposed order. Below are a few key examples and short explanations. For more information, please visit this webpage .
The deemed final order does not impose an upper limit on SPF values.
The proposed order, in contrast, proposes a maximum labeled SPF of 60+ and also proposes a maximum on the formulated SPF value of a sunscreen.
The deemed final order makes sunscreens containing 16 specified sunscreen active ingredients GRASE by incorporating the ingredients from the (not in effect) 1999 sunscreen monograph.
However, the proposed order proposes GRASE status for sunscreens containing zinc oxide and titanium dioxide; not GRASE status for sunscreens containing aminobenzoic acid and trolamine salicylate because of data showing safety issues; and not GRASE status for sunscreens containing cinoxate, dioxybenzone, ensulizole, homosalate, meradimate, octinoxate, octisalate, octocrylene, padimate O, sulisobenzone, oxybenzone, and avobenzone because of inadequate data to support a safety finding.
Consistent with the requirements in the labeling and effectiveness rule for sunscreens issued in 2011, the deemed final order does not require broad spectrum testing, but it creates an optional broad spectrum labeling claim and broad spectrum testing that is required to include this claim on labeling.
To address the growing evidence of significant harms associated with UVA exposure, the proposed order proposes a requirement that all sunscreens with SPF values of 15 and above satisfy broad spectrum requirements.
FDA will consider the on-time comments we received on the 2019 proposed rule as comments submitted on this proposed order. For this reason, FDA is asking people not to resubmit the same comments, or rewrites of the same comments, to the proposed order if they submitted those comments during the comment period for the 2019 proposed rule. This will make things easier for both the commenters and for FDA and will help keep the process moving quickly. In addition, this proposed order gives the public an opportunity to submit new information that has become available since the comment period closed on the 2019 proposed rule.
If at any time, sufficient evidence becomes available to answer the outstanding questions about whether a sunscreen containing any of these eight ingredients is GRASE, FDA plans to proceed to a final order reflecting our conclusion about that ingredient’s status. However, if there is not sufficient data to resolve the questions about each of these ingredients at the end of the proposed order comment period, FDA could consider deferring further action on the GRASE status of sunscreens containing the particular ingredient(s) to allow additional time for data to be developed and submitted. This would be the case if the agency has received adequate indication that the party seeking the deferral had made timely and diligent progress in trying to obtain that safety information.
In addition, if FDA initially defers further action regarding sunscreens containing a specific active ingredient, FDA plans to re-evaluate the progress of studies periodically. If FDA later decides that the studies are not progressing or otherwise are not productive, we expect we would move forward with a final order on sunscreens containing this ingredient. Moving forward, to make decisions on the GRASE status for OTC sunscreen products with certain active ingredients, the agency will use the administrative order process as established by the CARES Act. The statute gives FDA the authority to use the order process to add, remove or change conditions for an OTC monograph drug.
One thing — please protect yourself from the sun! Incidence rates for both melanoma and non-melanoma skin cancers have been rising for the past quarter century. The relationship between skin cancers and overexposure to the sun is well-documented.
Sun safety is important for everyone, including people of all skin tones. Consumers should continue to use sun protection measures, including using broad spectrum sunscreen of SPF 15 or higher, as we gather more safety data on sunscreen ingredients.
However, sunscreen is only one part of the solution. People should engage in sun protective behaviors, such as wearing protective clothing; wearing sunglasses and a hat that provides adequate shade; and finding shade whenever possible during periods of peak sunlight. Also, consumers should use adequate protection and appropriate precaution with sunlamps and tanning beds/booths. Both are sources of UV radiation that have been linked to skin cancer, skin burns, premature skin aging, and both short-term and long-term eye damage. More about sun protection and sunscreens is available on the FDA website . Check out these resources and stay safe in the sun.
The European Union (EU) aims for a tobacco use prevalence of less than 5% by 2040 with its Tobacco-Free Generation goal, aligning with the tobacco endgame approach. In the Joint Action on Tobacco Control 2 (JATC-2) -project, we examined adopted and planned endgame goals and measures as well as preparedness to counter tobacco industry interference in the process. We surveyed key informants in 24 out of 50 countries in the WHO European Region (19 of the 27 EU Member States, MS). Altogether, eight countries (7 EU MS) had official governmental endgame goals, and an additional six EU MS had similar proposals from government, civil society or research entities. Movement towards tobacco endgame was most evident in retail-oriented and consumer-oriented policies. These include restricting the sales of tobacco and related products and raising the age limit above 18 years. Product standards were used especially to regulate flavours but no measures to substantially reduce addictiveness were reported. Market-oriented measures that tap into industry profits were predominantly missing, and countries often lacked concrete tools to prevent industry interference. Respondents’ concerns around tobacco endgame were related to high smoking prevalence in some population groups, non-combustible and new nicotine products, cross-border marketing, political will, challenges with the existing regulations and industry interference. Results indicate both momentum and challenges in adopting and disseminating measures that facilitate achieving tobacco endgame goals. The EU goal can be used to advocate for national endgame goals and measures, and for the strengthened implementation of the WHO Framework Convention on Tobacco Control.
This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/ .
https://doi.org/10.1136/tc-2024-058606
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In the tobacco endgame approach, the focus is shifted from controlling the tobacco epidemic to ending it by reducing use to a minimal level in the population with structural, political and social changes. In the European Union, this is supported by the recently launched Tobacco-Free Generation goal.
Tobacco endgame is well aligned with the WHO Framework Convention on Tobacco Control, which encourages parties to implement measures beyond the convention to better protect human health and obliges them to adopt effective measures to prevent and reduce nicotine addiction besides tobacco consumption.
While several European countries already have governmental tobacco endgame goals or proposals towards these, there is substantial variation in their definitions, timelines and coverage of tobacco and nicotine products.
Adopted and planned tobacco endgame measures centre around product-oriented, retail-oriented and consumer-oriented policies, such as product standards to reduce appeal, restricting sales and increasing the age limit above 18 years.
Knowledge sharing facilitates the dissemination of tobacco endgame approach.
More focus is needed on measures that can be expected to have a substantial impact on product availability, appeal and addictiveness.
Concrete tools to prevent and counter tobacco industry interference are needed, as it is seen as a clear challenge in tobacco endgame.
In the WHO European Region, encompassing 53 countries including 27 European Union (EU) Member States, 25% of adults use tobacco. 1 This prevalence ranks second highest among the WHO regions, with a relatively slow decline compared with other regions. In 2021, as part of Europe’s Beating Cancer Plan, the EU announced a ‘Tobacco-Free Generation’ goal for the region. 2 While the concept of tobacco-free generation originates in a proposal to limit tobacco sales by year born, 3 the EU goal is defined as less than 5% of the population using tobacco by 2040. The EU goal aligns with the tobacco endgame approach, where the focus shifts from controlling the tobacco epidemic to ending it by reducing use to a minimal level in the population with structural, political and social changes. 4 The EU goal is well justified under the WHO Framework Convention on Tobacco Control (WHO FCTC), which encourages parties to implement measures beyond the convention to better protect human health (Article 2.1) and obliges them to adopt effective measures and cooperate in developing appropriate policies to prevent and reduce tobacco consumption, nicotine addiction and exposure to tobacco smoke (Article 5.2b). 5 Several European countries have already set their national tobacco endgame goals prior to the EU goal. 6 We examine the current status of adopted and planned national goals and measures in the WHO European region, and how these reflect the EU goal among the Member States. We also examine how experts perceive the likelihood of adopting or achieving the endgame goal in their own country, and countries’ preparedness to counter tobacco industry interference in the process.
In the Joint Action on Tobacco Control 2 (JATC-2) project, 7 Work Package 9 (WP9) is tasked to identify national tobacco endgame strategies and forward-looking tobacco control policies, to explore and exchange best practices in the development, implementation and evaluation of these strategies and policies, and to facilitate their development in the European region. The WP9 involves 21 partner organisations from 15 European countries (Belgium, Cyprus, Denmark, Finland, France, Greece, Hungary, Ireland, Italy, Lithuania, Norway, Portugal, Serbia, Slovenia and Spain), with the Netherlands collaborating. As part of this work, we surveyed key tobacco control informants in the WHO European region between 15 September 2022 and 13 January 2023.
Key informants consisted primarily of national WHO FCTC focal points, who are nominated by their country to participate in the official treaty reporting. Contacting them was made possible through assistance from the WHO FCTC Knowledge Hub on Surveillance and Convention Secretariat. In the absence of a functional contact with the focal point (eg, due to personnel changes), other national tobacco control experts were identified with assistance from JATC-2 partners and the WHO European Office for the Prevention and Control of Noncommunicable Diseases. We excluded Switzerland and Monaco due to lack of contacts, and the Russian Federation due to the suspension of research collaboration because of the war in Ukraine. From each country, one coordinated response was requested if the respondent engaged other stakeholders. The questionnaire gathered information and expert opinions on national-level policies and was, therefore, not subjected to an ethics approval. Respondents gave an informed consent on their participation.
Responses were received from 24 of 50 countries (19 of 27 EU Member states), with response rates of 48% across the region and 70% within the EU. The respondents were from Austria, Azerbaijan, Belgium, Cyprus, Czechia, Denmark, Estonia, Germany, Finland, France, Hungary, Ireland, Italy, Lithuania, Luxembourg, the Netherlands, North Macedonia, Norway, Portugal, Serbia, Slovenia, Spain, Sweden and Uzbekistan. The majority of the respondents were officials from health ministries/departments/directorates in the government. One respondent was from the interior ministry, two from national authorities specialised in addictions or substance use and one from a public health institute. Respondents were contacted back in March 2023 for potential updates, which were received from Uzbekistan. The JATC-2 partners could further update the information on new national policies up to May 2024. Partner updates were provided by Belgium, Finland, France, Ireland, the Netherlands, Norway, Slovenia and Spain.
The questionnaire assessed the existence of national tobacco endgame goals, their definition, the selected time frame, tobacco or nicotine products covered by the goals and the perceived likelihood of adopting/achieving these goals (from 0=very unlikely to 10=very likely). The reason for the selected response was asked. Furthermore, we inquired about adopted or planned endgame measures and measures to prevent industry interference ( table 1 ). The endgame measures for the questionnaire were identified from earlier reviews. 4 8 In WP9, harm reduction measures are outside the scope of work and were, therefore, not included in the questionnaire. The measures on tobacco industry interference were derived from screening the recommendations of the WHO FCTC Article 5.3 guidelines. Some additional measures of interest to WP9 partners were also added (marked with * in table 1 ). The questionnaire and more details of its development are available in the WP9 indicator compendium at www.jaotc.eu . 9
Measures included in the JATC-2 WP9 questionnaire
We describe adopted goals and measures based on respondent-provided details supplemented with publicly available information on the goals and measures (from, eg, governmental and EU websites). For plans or proposals, we disclose country names only if the information is publicly available to prevent industry interference. We present quotes from the experts’ open-ended responses. This article does not seek to present an exhaustive list of endgame goals and measures in Europe but provides examples and experiences, which can help draw an overview of their status and future directions.
Official goals adopted or acknowledged by governments.
Altogether eight countries reported official tobacco endgame goals ( table 2 ). These were divided into general population goals without subgroup targets and goals including certain generations or subgroups. Most of the countries are aiming for less than 5% prevalence of use, but three countries aim at no use at all in certain subgroups addressing children or pregnant women. Three countries define their prevalence goals specifically as daily use. All countries except Norway have set a target year between 2025 and 2040. The official definitions focus on smoking or tobacco use, except for three countries that also mention nicotine products or tobacco-related products. Some countries extend the scope of endgame compared with the main definition: Belgium and the Netherlands reported including all tobacco and non-pharmaceutical nicotine products, while France and Norway also reported including heated tobacco products (HTPs) under their smoking targets. Finland and Norway have integrated the endgame goal into the objective of the tobacco control law.
Official tobacco endgame goals among the countries responding to the JATC-2 WP9 questionnaire
Altogether seven countries reported endgame proposals from their countries. In Denmark, the former government introduced a Nicotine-Free Generation goal where no one born since 2010 should start smoking or using nicotine products, 10 but this proposal has not progressed. A strategy for tobacco-free Germany by the German Cancer Research Center, supported by several NGOs and research entities, aims for <5% adult and <2% adolescent prevalence in tobacco and non-pharmaceutical nicotine use by 2040. 11 Additionally, the German government’s strategy for the Sustainable Development Goals contains a goal close to the common endgame prevalence level, namely, of 7% smoking prevalence among youth by 2030. 12 In Italy, scientific societies and independent scientists have allied to advocate for the development of a national tobacco endgame strategy. 13 In Spain, a new comprehensive plan for the prevention and control of tobacco for years 2024–2027 includes a goal to achieve <5% prevalence of daily use among 14–18-year olds. 14 Previously, public health organisations and civil society associations published an endgame declaration calling for a goal of <5% smoking prevalence by 2030 and 2% by 2040 in Spain. 15 Two other countries reported that an endgame proposal exists but is not yet publicly available. One was part of national health strategy discussions, where a goal in line with the EU goal has been proposed. From the second, no details were provided.
Among the respondents from eight countries with official endgame goals, six provided a score for the likelihood of achieving their goal. On a scale of 0–10, the responses were either 6 (three countries) or 7 (three countries), reflecting moderately positive expectations. Concerns were expressed in relation to non-combustible and new nicotine products, differences between population groups, industry interference, cross-border marketing and sales, sustaining the political will and challenges in estimating the impact of the measures ( table 3 ).
Respondents’ reflections on the perceived likelihood of achieving their official governmental tobacco endgame goals (six countries, panel A), and on the perceived likelihood of adopting such goals in their country (12 countries, panel B).
Among 12 of the 16 countries without an endgame goal who provided a score, the expectations of adopting such a goal in their own country varied greatly: from very negative 0–2 (five countries) and somewhat unsure 5 (three countries) to rather positive 7–8 (two countries). Two countries perceived the adoption very likely, scoring 10. Concerns among these countries related to lack of political will, industry interference and problems in current tobacco control processes, shifting the focus to the COVID-19 pandemic, and the current high use of tobacco and related products ( table 3 ). Some countries reported a preference for general addiction or non-communicable disease (NCD) prevention strategies over tobacco control strategies. Having previously established governmental prevalence reduction goals in a cross-cutting way was seen as a strength for moving towards an endgame approach.
Independently of whether a national tobacco endgame goal exists, a few measures that can contribute to such a goal were already implemented to some extent. These are presented in table 4 according to the taxonomy set in table 1 and summarised below.
Adopted and planned tobacco endgame measures and forward-looking tobacco control measures among the countries responding to the JATC-2 WP9 questionnaire
The EU Tobacco Products Directive (TPD) and the delegated directive 2022/2100 prohibit characterising flavours in cigarettes, roll-your-own and HTPs, but some countries go beyond this to reduce product appeal with different product standards. Five countries had fully prohibited menthol as an additive that facilitates inhalation in combustibles, and seven countries had prohibited all or most flavours in e-cigarette liquids ( table 4 ). These measures were also planned in some countries, and Finland was processing regulation on nicotine pouch flavours. Plain packaging had been extended from tobacco products to e-cigarette packaging in three countries and was also considered for nicotine pouch packaging in two. Some countries had standardised or were standardising the appearance of individual cigarettes, nicotine e-liquids, e-cigarette refill containers and/or nicotine pouches. Health warnings on individual cigarette sticks were considered in Norway, which had also prohibited imports and sales of waterpipe tobacco, therefore partially addressing a ban on combustibles.
The TPD allows Member States to prohibit a certain category of tobacco or related products if the Commission approves it after considering whether national provisions are justified, necessary and proportionate, and whether they constitute a disguised barrier to trade. Belgium has received approval to prohibit disposable e-cigarettes, and two other countries also have proposals to introduce such a ban. Two countries reported an authorisation scheme for novel tobacco products, where the government authorises or rejects market entry applications. Non-pharmaceutical nicotine products (other than e-cigarettes) are not under TPD and countries regulate their market entry independently. An authorisation scheme for novel nicotine products was reported by two countries. Two countries have prohibited nicotine pouches. One country reported considering a ban on products that do not fall into existing product categories or are placed on the market after a certain date, but no specification was available.
Some countries reported prohibiting or restricting tobacco or related product sales in retail types or locations related to minors, and Cyprus was planning to restrict points of sales near schools ( table 4 ). Broader restrictions were still rare. New stepwise sales reductions were adopted in two countries, and a substantial reduction in retailers was set to the strategy in Norway but without concrete proposals. Two countries limited tobacco sales to specialist shops, and one country was considering including also e-cigarette sales to these. Hungary has set numerical limits to the density of the specialist tobacco shops. Finland introduced high annual supervisory fees to retail license holders and has had a proposal to prohibit the granting of a retail license to temporary and mobile sales places. France supported the transition of tobacco retailers into other local shops and no longer selling tobacco.
Most of the proposed endgame measures in these categories were not in place or planned. Plans focused on consumer-oriented measures, mainly age limits of 20 or 21 years, where altogether six countries have had proposals to raise the age of sale above 18. Of these, Ireland already approved in May 2024 a proposal for legislation that will increase the age of sale of tobacco to 21, aiming to be the first EU country to do so. 16 In Norway, a tobacco-free and nicotine-free generation to those born in 2010 is envisaged in a national strategy, but decisions and details on its implementation are awaited. In Denmark, the new prevention agreement proposes prohibiting the import, purchase and possession of nicotine products that are illegal to market in the country. Sweden is utilising excise duty for curtailing industry to set its own retail prices. Five countries have a regulated market model where the state has a monopoly on tobacco sales.
While many respondents referred to implementing Article 5.3 of the WHO FCTC, concrete tools to prevent industry interference were often missing. However, some examples of adopted measures were shared. These addressed legislative measures, lobbying registers, a code of conduct/procedure, public disclosure of necessary correspondences, disclosure of lobbying expenses, plans to better regulate production and industry reporting obligations, and ethical guidelines preventing state investments in the tobacco industry ( table 5 ). As for planned measures, three countries were developing guidelines on contact between the industry and governmental organisations, one country was planning to develop a transparency register of contacts between the tobacco industry and government, and another country for the disclosure of the records from necessary interactions.
Regulations and measures to prevent tobacco industry interference among the countries responding to the JATC-2 WP9 questionnaire
Our results indicate both momentum and challenges in adopting and disseminating measures that facilitate achieving the EU Tobacco-Free Generation goal of less than 5% tobacco use by 2040. Almost half of the 27 EU Member States either have already adopted a national tobacco endgame goal or have a proposal for such a goal from the government, civil society or research entities. Outside the EU in the WHO European Region, Norway reported an official tobacco endgame goal. While most of the countries with an official goal aim for a similar <5% prevalence level as the EU goal, the definitions of goals and their specifications in the government documents vary considerably. For some countries, this can also pose challenges in measuring the progress. In Ireland and Sweden, the target year of 2025 is approaching soon, calling for the first comprehensive evaluations of national tobacco endgame strategies in the region. Including tobacco endgame as an objective of tobacco control legislation—like in Finland and Norway—may provide sustainability behind changing governmental programmes or strategies and political will.
In the EU, the Member States have benefitted from common minimum product standards set in the TPD. While several countries already go beyond the TPD to address attractiveness and appeal, no measures that would substantially reduce addictiveness were adopted or planned. To meet the <5% prevalence level by 2040, the TPD should be developed from this perspective in a forward-looking way. The EU has invested substantial effort and resources into the advisory mechanism for the prohibition of characterising flavours. 17 Yet a simplified, effective approach would be to follow the WHO FCTC Article 9 and 10 guidelines to prohibit the use of all ingredients that make tobacco products attractive, including flavouring agents. Furthermore, the EU-level nicotine limits for cigarettes could be lowered to make them less or non-addictive, leading to their gradual phase-out from the market. Based on the evidence, reducing nicotine content in cigarettes to very low levels could improve public health and have benefits across different population groups by decreasing the uptake of regular smoking, decreasing the amount smoked and increasing smoking cessation. 18 Introducing very low nicotine cigarettes on the EU level could be a balanced and justified measure considering the increased product supply caused by the continuous entrance of novel tobacco or nicotine products to the market. These novel products were mainly seen as challenges in tobacco endgame by the respondents, and several countries are already covering nicotine products such as e-cigarettes and nicotine pouches in their endgame goals or measures. This can be seen as a forward-looking approach to respond to tobacco industry strategies, which aim to increase product portfolio and profit, attract new customers and delay and distract from effective control policies. 19 Clear separation between measures to only reduce harm and measures to end the tobacco epidemic may help regulators and policymakers to understand and identify measures that are feasible and likely to produce substantial impact in their local context.
The reported retail-oriented and consumer-oriented measures tended to focus on reducing the sales points by limiting sales to certain retailers and raising the age limit of sales above 18 years. For example, substantial stepwise reductions in retail outlets are beginning to be implemented in the Netherlands and in Belgium. Yet, most countries in the region would still need to introduce retail licensing to effectively control and reduce retail density. 20 In Finland, the licensing with high annual costs has gradually reduced the number of tobacco retailers to approximately a half. However, the number remains high and unequally distributed to more socioeconomically disadvantaged areas—reminding of the continued need to consider the impact of tobacco endgame measures in different population groups. 21 In Hungary, the introduction of state-owned specialist tobacco shops has decreased the density of tobacco shops by 85%, concurring with declining adolescent smoking. 22 The age limits that were under consideration focused on 20 or 21 years. In the European context, where no country yet has implemented an age limit above 18 years for tobacco, this measure could have a substantial impact considering most of the initiation occurs by the age of 20. 23 24 In Europe, Norway was first to publish in March 2023 a goal that children born since 2010 do not use tobacco and nicotine products, but its practical implementation is undecided. 25 The United Kingdom has then moved ahead by announcing in October 2023 that it will become an offence to sell tobacco products to anyone born on or after 1 January 2009. 26 Based on the evidence, the retail- and consumer-oriented measures, especially if combined, can be expected to have a notable impact on tobacco use prevalence and lead to health gains over time. 23 27
The EU goal can be used to support the development of similar national goals. Additionally, it can be used to bring the need for better implementation of the WHO FCTC to the political agenda, connected to the national work for NCD prevention and sustainable development goals. This can be beneficial especially in countries where adopting an endgame goal is not yet seen as feasible in the current tobacco control context. The implementation of the WHO FCTC as well as the capacity for tobacco control needs to be strengthened in Europe. 28 As part of this, countries should look into measures that tap into tobacco industry profits, which are mostly not even planned in the region. Together with the lack of concrete tools to prevent and counter industry interference, this enables the industry to mobilise resources for lobbying and distracting policymaking away from timely and effective measures. Industry interference was identified as a challenge both in adopting and achieving tobacco endgame goals. Better protection is needed even on the EU level, as shown in the recent European Ombudsman investigations. 29 Besides national actions, the EU-level investment and support for the enforcement of tobacco control, together with the regular revision of key directives and recommendations, are essential for achieving the EU goal. An interesting comparison can be found in food safety where the EU audits the application and effectiveness of the laws and controls and provides training to the responsible authorities. 30
Finally, the EU goal can be used to raise awareness of the tobacco endgame approach, leveraging support from civil society and the public. For instance, a study from Ireland showed low awareness but broad support for the local tobacco endgame goal. 31 In the Netherlands, key factors in accelerating tobacco control have been the genesis of a ‘Smoke-free Generation’ movement in the wider society, initiated by the three main national charities, combined with stricter adherence to Article 5.3 of the WHO FCTC and a comprehensive marketing ban. 32 In 2022, several European civil society associations launched a joint European Citizen’s Initiative calling for a broad range of measures including tobacco-free environments and ending the sale of tobacco and nicotine products to citizens born since 2010, but it did not reach enough signatories. 33 To facilitate the dissemination of measures that are likely to have a substantial impact within a reasonable timeframe, knowledge sharing between countries with different tobacco control contexts and approaches is needed. Multinational collaborations such as the JATC-2 can serve as platforms to share best practices and act as vehicles to overcome the barriers of lack of knowledge or political will. A great global opportunity for information exchange presents in the 11th session of the Conference of the Parties of the WHO FCTC in 2025, where an expert group established by the COP10 will present its report on Article 2.1 and forward-looking tobacco control measures. 34 The possibility of shifting the focus from controlling to ending the tobacco epidemic is an important message to convey to policymakers.
Patient consent for publication.
Not applicable.
This study gathered only information on national-level policies and expert opinions related to these and was therefore not subject to ethics approval. Participants gave informed consent to participate in the study before taking part.
The authors want to thank all the respondents of the questionnaire. The authors are grateful for the support and contributions from all JATC-2 WP9 partners in the development of the questionnaire and provision of feedback to the analysis and reporting of the results as part of the project reporting and deliverable drafting. Further, the authors are grateful for the support from the WHO FCTC Knowledge Hub on Surveillance, the Secretariat of the WHO FCTC and the WHO NCD Office in identifying the contacts for the questionnaire.
Collaborators Co-authors of the Work Package 9 of the Joint Action on Tobacco Control 2 (JATC-2) -project: Adrián González-Marrón (Group of Evaluation of Health Determinants and Health Policies, Department of Basic Sciences, Universitat Internacional de Catalunya, Sant Cugat del Vallès, Spain), Alessandra Lugo (Department of Medical Epidemiology; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy), Angeliki Lambrou (Directorate of Epidemiology and Prevention of Non-Communicable Diseases and Injuries, National Public Health Organization (NPHO), Athens, Greece), Anna Mar Lopez Luque (Grupo de Investigación en Control del Tabaco, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, (CIBERES), Madrid, Spain; Programa de Prevenció i Control del Càncer, Institut Català d'Oncologia, L'Hospitalet de Llobregat, Barcelona, Spain), Armando Peruga (Grupo de Investigación en Control del Tabaco, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain, Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, (CIBERES), Madrid, Spain; Centro de Epidemiología y Políticas de Salud, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago, Chile), Biljana Kilibarda,(Institute of Public Health of Serbia “Dr Milan Jovanovic Batut”, Belgrade, Serbia), Cristina Lidón-Moyan (Group of Evaluation of Health Determinants and Health Policies, Department of Basic Sciences, Universitat Internacional de Catalunya, Sant Cugat del Vallès, Spain), Daniela Alejandra Blanco-Escauriaza (Group of Evaluation of Health Determinants and Health Policies, Department of Basic Sciences, Universitat Internacional de Catalunya, Sant Cugat del Vallès, Spain), Dolors Carnicer-Pont (Grupo de Investigación en Control del Tabaco, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, (CIBERES), Madrid, Spain; Programa de Prevenció i Control del Càncer, Institut Català d'Oncologia, L'Hospitalet de Llobregat, Barcelona, Spain), Efstathios Papachristou (Directorate of Epidemiology and Prevention of Non-Communicable Diseases and Injuries, National Public Health Organization (NPHO), Athens, Greece), Elena Demosthenous (Cyprus National Addictions Authority, Nicosia, Cyprus), Emilia Nunes (General Directorate of Health, Ministry of Health, Lisbon, Portugal), Esteve Fernández (Grupo de Investigación en Control del Tabaco, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Respiratorias, (CIBERES), Madrid, Spain; Programa de Prevenció i Control del Càncer, Institut Català d'Oncologia, L'Hospitalet de Llobregat, Barcelona, Spain; School of Medicine and Health Sciences, Campus de Bellvitge, Universitat de Barcelona, L’Hospitalet de Llobregat, Spain), Giulia Carreras (Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy), Giuseppe Gorini (Institute for Cancer Research, Prevention and Clinical Network (ISPRO), Florence, Italy), Helma Slingerland (Ministry of Health, Welfare and Sport, the Hague, the Netherlands), Judit Tisza (National Korányi Institute of Pulmonology, Budapest, Hungary), Lorenzo Spizzichino (Ministry of Health, Rome, Italy), Maria-Alejandra Cardenas (Ministry of Health and Prevention, Paris, France), Maria Karekla (University of Cyprus, Nicosia, Cyprus), Maurice Mulcahy (National Environmental Health Service, Health Service Executive (HSE), Galway Business Park, Dangan, Ireland), Milena Vasic (Institute of Public Health of Serbia “Dr Milan Jovanovic Batut”, Belgrade, Serbia), Salla-Maaria Pätsi (Department of Public Health and Welfare, Finnish Institute for Health and Welfare, Helsinki, Finland), Silvano Gallus (Department of Medical Epidemiology; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy), Sotiria Schoretsaniti (Directorate of Epidemiology and Prevention of Non-Communicable Diseases and Injuries, National Public Health Organization (NPHO), Athens, Greece), Zsuzsa Cselkó (National Korányi Institute of Pulmonology, Budapest, Hungary).
Contributors Salla-Maaria Pätsi conducted initial analyses from the data. HO analysed the data for this manuscript and wrote the first draft. OR, TL and HK reviewed the first draft. HO developed and revised the following drafts as per the review and contributions from all other authors. All authors approved the final version of the paper. HO is responsible for the overall conduct of the study and the contents of this manuscript.
Funding This work was supported by the European Union’s Health Program (2014-2020) under grant agreement N°101035968. The content of this document represents the views of the authors only and is their sole responsibility; it cannot be considered to reflect the views of the European Commission and/or the European Health and Digital Executive Agency (HaDEA) or any other body of the European Union. The European Commission and the Agency do not accept any responsibility for use that may be made of the information it contains. DCP, AML and EF are partly supported by the Ministry of Universities and Research, Government of Catalonia (grant number: 2021SGR00906) and thank the CERCA programme for institutional support to IDIBELL.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer-reviewed.
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Common types of limitations and their ramifications include: Theoretical: limits the scope, depth, or applicability of a study. Methodological: limits the quality, quantity, or diversity of the data. Empirical: limits the representativeness, validity, or reliability of the data. Analytical: limits the accuracy, completeness, or significance of ...
Limitations in Research. Limitations in research refer to the factors that may affect the results, conclusions, and generalizability of a study. These limitations can arise from various sources, such as the design of the study, the sampling methods used, the measurement tools employed, and the limitations of the data analysis techniques.
Research limitations are one of those things that students tend to avoid digging into, and understandably so. No one likes to critique their own study and point out weaknesses. Nevertheless, being able to understand the limitations of your study - and, just as importantly, the implications thereof - a is a critically important skill. In this post, we'll unpack some of the most common ...
Methodology limitations. Not having access to data or reliable information can impact the methods used to facilitate your research. A lack of data or reliability may limit the parameters of your study area and the extent of your exploration. Your sample size may also be affected because you won't have any direction on how big or small it ...
The limitations of the study are those characteristics of design or methodology that impacted or influenced the interpretation of the findings from your research. Study limitations are the constraints placed on the ability to generalize from the results, to further describe applications to practice, and/or related to the utility of findings ...
The ideal way is to divide your limitations section into three steps: 1. Identify the research constraints; 2. Describe in great detail how they affect your research; 3. Mention the opportunity for future investigations and give possibilities. By following this method while addressing the constraints of your research, you will be able to ...
First and foremost, they navigate informational limitations, work around knowledge gaps when designing studies, formulating hypotheses, and analyzing data. They also handle technical limitations, making the most of what their hands, equipment, and instruments can achieve. Finally, researchers must also manage logistical limitations.
In research, studies can have limitations such as limited scope, researcher subjectivity, and lack of available research tools. Acknowledging the limitations of your study should be seen as a strength. It demonstrates your willingness for transparency, humility, and submission to the scientific method and can bolster the integrity of the study.
3. Identify your limitations of research and explain their importance. 4. Provide the necessary depth, explain their nature, and justify your study choices. 5. Write how you are suggesting that it is possible to overcome them in the future. Limitations can help structure the research study better.
Research Limitations. Research limitations are, at the simplest level, the weaknesses of the study, based on factors that are often outside of your control as the researcher. These factors could include things like time, access to funding, equipment, data or participants.For example, if you weren't able to access a random sample of participants for your study and had to adopt a convenience ...
Answer: The limitations of a study are its flaws or shortcomings which could be the result of unavailability of resources, small sample size, flawed methodology, etc. No study is completely flawless or inclusive of all possible aspects. Therefore, listing the limitations of your study reflects honesty and transparency and also shows that you ...
Limitations. Limitations of a dissertation are potential weaknesses in your study that are mostly out of your control, given limited funding, choice of research design, statistical model constraints, or other factors. In addition, a limitation is a restriction on your study that cannot be reasonably dismissed and can affect your design and results.
build reviewers' trust in you and your research, discussing every drawback, no matter how small, can give the impression that the study is irreparably flawed. For each limitation you identify, provide a sentence that refutes the limitation or that provides information to counterbalance or otherwise minimize the limitation's perceived impact.
Abstract. Study limitations represent weaknesses within a research design that may influence outcomes and conclusions of the research. Researchers have an obligation to the academic community to present complete and honest limitations of a presented study. Too often, authors use generic descriptions to describe study limitations.
Research limitations in a typical dissertation may relate to the following points: 1. Formulation of research aims and objectives. You might have formulated research aims and objectives too broadly. You can specify in which ways the formulation of research aims and objectives could be narrowed so that the level of focus of the study could be ...
dangerous than limitations that cause a bias away from the null. On the other hand, limitations that lead to a conclusion that your exposure impacts your outcome when it does not (i.e., a bias away from the null) are often considered more dangerous. Imagine a proposal to conduct a prospective study of postmenopausal
Writing a Research Proposal; Acknowledgements; Definition. ... A Note about Sample Size Limitations in Qualitative Research. Sample sizes are typically smaller in qualitative research because, as the study goes on, acquiring more data does not necessarily lead to more information. This is because one occurrence of a piece of data, or a code, is ...
The purpose of the research proposal (its job, so to speak) is to convince your research supervisor, committee or university that your research is suitable (for the requirements of the degree program) and manageable (given the time and resource constraints you will face). The most important word here is "convince" - in other words, your ...
Writing the limitations of the research papers is often assumed to require lots of effort. However, identifying the limitations of the study can help structure the research better. Therefore, do not underestimate the importance of research study limitations. 3. Opportunity to make suggestions for further research.
Research proposal examples. Writing a research proposal can be quite challenging, but a good starting point could be to look at some examples. We've included a few for you below. Example research proposal #1: "A Conceptual Framework for Scheduling Constraint Management".
1 Answer to this question. Answer: In a proposal, limitations are the constraints of the study, that is, aspects of the study not covered for various reasons. These could pertain to subjects, geography, data, and so on. For instance, one limitation could be that the study will only look at people of a certain age group or income level.
Delimitations refer to the specific boundaries or limitations that are set in a research study in order to narrow its scope and focus. Delimitations may be related to a variety of factors, including the population being studied, the geographical location, the time period, the research design, and the methods or tools being used to collect data.
Research proposals can vary depending on the nature of the research project and the specific requirements of the funding agency, academic institution, or research program. ... Address any potential limitations or challenges that may be encountered. Resources: Identify the resources required to conduct the research, such as funding, equipment ...
The research started after surveys showed managers saw less creativity from their teams when workers were remote. More than 36 million employees will work remotely by 2025, according to research.
Please note several limitations on length: (1) your abstract should be no more than 150 words, as the abstract will also be used for the conference program, (2) your completed research paper should be no more than 10 pages (approx. 5,000 words, including figures, tables, references, and appendices).
Today, the U.S. National Science Foundation, in partnership with the American Association of Community Colleges (AACC), announced the three winning teams of the 2024 Community College Innovation Challenge (CCIC). The annual competition seeks to strengthen entrepreneurial thinking among community college students by challenging them to develop STEM-based solutions to real-world problems.
Overview: 8 Research Proposal Killers. The research topic is too broad (or just poorly articulated). The research aims, objectives and questions don't align. The research topic is not well justified. The study has a weak theoretical foundation. The research design is not well articulated well enough. Poor writing and sloppy presentation.
The deemed final order does not impose an upper limit on SPF values. The proposed order, in contrast, proposes a maximum labeled SPF of 60+ and also proposes a maximum on the formulated SPF value ...
In 2021, as part of Europe's Beating Cancer Plan, the EU announced a 'Tobacco-Free Generation' goal for the region.2 While the concept of tobacco-free generation originates in a proposal to limit tobacco sales by year born,3 the EU goal is defined as less than 5% of the population using tobacco by 2040.