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Please ensure that anything you submit to The BMJ conforms to the International Committee of Medical Journal Editors’ Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly work in Medical Journals uniform recommendations for manuscripts submitted to biomedical journals.
Before submitting an article, please ensure that you have followed all guidelines below. We recommend learning about our house style and ways to incorporate images into your submission .
The title should be informative and, for research papers, a subtitle with the study design (for example, "a phase III clinical trial" or "a systematic review and meta-analysis").
In this page, please provide for each author his or her name, affiliation (job title) at the time the paper was written, email and, for the corresponding author, the best contact address. All authors must fulfill the ICMJE criteria for authorship . If the number of authors is very large we may ask for confirmation that everyone listed met the ICMJE criteria for authorship . We also offer the option of joint first authorship when two authors meet criteria for such a designation. We reserve the right to require that authors form a group whose name will appear in the article byline. MEDLINE guidance explains that group authorship is acceptable, stating "When a group name for a specific consortium, committee, study group, or the like appears in an article byline, the personal names of the members of that group may be published in the article text. Such names are entered as collaborator names for the MEDLINE citation."
Further details about The BMJ 's stance on authorship, contributorship, and group authorship can be found on our Authorship and contributorship page.
Please note that from 30 November 2018 The BMJ is mandating ORCiD iDs for corresponding authors for all research articles if accepted, and this information will be required alongside submitted manuscripts. Co-authors and reviewers are strongly encouraged to also connect their ScholarOne accounts to ORCiD. We firmly believe that the increased use and integration of ORCiD iDs will be beneficial for the whole research community. For those who do not currently have an iD they will be required to register but this is free and takes a matter of seconds - we strongly encourage all authors to register for an ORCiD profile .
To learn more about ORCiD, please visit http://orcid.org/content/initiative
If article describes a study please include the study design | |
Separate with commas. No full stops after initials. If there is a very large number of authors we may suggest that they form a group whose name will appear in the article byline. List ORCiD iD alongside respective authors | Ingela Radestad (0000-0000-0000-0000), Gunnar Steineck, C Nordin, B Sjogren |
Separate each part of address with a comma (don't use a separate line for each part) Please include postcodes Use same style of name as below title Please give one job position for each author, (under the relevant address) on separate line from author's name | Centre for Caring Sciences, Karolinska Institute, S-171 76 Stockholm, Sweden Ingela Radestad midwife Unit of Cancer Epidemiology, Radiumhemmet, Karolinska Institute Gunnar Steinbeck associate professor Department of Womens Health, Karolinska Institute B Sjogren associate professor Department of Psychiatry, University Hospital, Linkoping, Sweden C Nordin associate professor |
Give the name, full address and email address of the corresponding author. Please note, there can only be one corresponding author per article. | Correspondence to: I Radestad iradestad@....... |
Each contributorship statement should make clear who has contributed what to the planning, conduct, and reporting of the work described in the article, and should identify one, or occasionally more, contributor(s) as being responsible for the overall content as guarantor(s). The guarantor accepts full responsibility for the work and/or the conduct of the study, had access to the data, and controlled the decision to publish. The following line should also be included - "The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted."
For articles in The BMJ that do not report original research - such as editorials, clinical reviews, and education and debate - please state who had the idea for the article, who performed the literature search, who wrote the article, and who is the guarantor (the contributor who accepts full responsibility for the finished article, had access to any data, and controlled the decision to publish). For non-research articles that include case reports such as lessons of the week, drug points, and interactive case reports, please also state who identified and/or managed the case(s). We encourage authors to fully acknowledge the contribution of patients and the public to their research where appropriate.
Since January 2000, The BMJ has not asked authors of journal articles to assign us their copyright and authors (or their employers) retain their copyright in the article. All we require from authors is an exclusive licence (or, from government employees who cannot grant this, a non-exclusive licence) that allows us to publish the article in The BMJ (including any derivative products) and any other BMJ products (such as the Student BMJ or overseas editions), and allows us to sublicense such rights and exploit all subsidiary rights.
We ask the corresponding author to grant this exclusive licence (or non-exclusive for government employees) on behalf of all authors by reading our licence and inserting in the manuscript on submission the following statement:
“The Corresponding Author has the right to grant on behalf of all authors and does grant on behalf of all authors, a worldwide licence to the Publishers and its licensees in perpetuity, in all forms, formats and media (whether known now or created in the future), to i) publish, reproduce, distribute, display and store the Contribution, ii) translate the Contribution into other languages, create adaptations, reprints, include within collections and create summaries, extracts and/or, abstracts of the Contribution, iii) create any other derivative work(s) based on the Contribution, iv) to exploit all subsidiary rights in the Contribution, v) the inclusion of electronic links from the Contribution to third party material where-ever it may be located; and, vi) licence any third party to do any or all of the above."
This licence allows authors to use their own articles for their own non-commercial purposes without seeking permission from us. Only if the use is commercial do we need to know about it. In addition, we will pay authors a royalty on certain commercial uses that we negotiate.
Information on permissions for authors and third parties for reuse can be found here .
Manuscripts authored or co-authored by one or more NIH employees must be submitted with a completed and signed NIH Publishing Agreement and Manuscript Cover Sheet according to NIH’s Employee Procedures .
Publication of any personal information about a patient in The BMJ - for example, in a case report or clinical photograph - will normally require the signed consent of the patient. If this is the case, please include a statement that any identifiable patients have provided their signed consent to publication and submit, as a supplemental file, The BMJ 's patient consent form that is available in several languages .
A competing interest - often called a conflict of interest - exists when professional judgment concerning a primary interest (such as patients' welfare or the validity of research) may be influenced by a secondary interest (such as financial gain, academic promotion, or personal rivalry). It may arise for the authors of an article in The BMJ when they have a financial interest that may influence, probably without their knowing, their interpretation of their results or those of others.
We believe that, to make the best decision on how to deal with an article, we should know about any competing interests that authors may have, and that if we publish the article readers should know about them too. We are not aiming to eradicate such interests across all article types in The BMJ . However, certain articles (see below) fall under a stricter policy announced in 2014 . This means that authors whose financial conflicts of interest are judged to be relevant by the BMJ team are not permitted to write these articles. We also ask our staff and reviewers to declare any competing interests.
A declaration of interests for all authors must be received before an article can be reviewed and accepted for publication. It should take one of two forms, depending on what type of article you are submitting. The links to the relevant forms are provided at the end of this section.
Since 2014, The BMJ requires that such articles must be written by authors without relevant financial ties to industry . By "industry" we mean companies producing drugs, medical foods, nutraceuticals, devices, apps or tests; medical education companies; or other companies with a financial or reputational interest in the topic of the article. We consider the following relationships with industry to be relevant, making it unlikely that we would be able to publish your work: employment; ownership of stocks and shares (this excludes mutual funds or other situations in which the person is not in a position to control investment decisions) ; travel and accommodation expenses; paid consultancy or directorship; patent ownership; aid membership of speakers' panels or bureaus and advisory board; acting as an expert witness ; being in receipt of a fellowship, equipment, writing, or administrative support; writing or consulting for a medical education promotional or communications company. If you are in doubt about the relevance of any potential conflict of interest please discuss with the editor of the appropriate section before submission.
All authors must review the updated COI policy and complete The BMJ 's Education Declaration of Interests form . If the article is accepted for publication these completed forms will be stored and made available on request. The corresponding author should insert within their manuscript a summary statement derived from the information provided in the COI forms (link below): " I/We have read and understood BMJ policy on declaration of interests and declare the following interests: [list them or state that you have none]."
Examples of different sorts of summary statements:
No competing interests : "We have read and understood BMJ policy on declaration of interests and declare that we have no competing interests."
Competing interests disclosed: " We have read and understood BMJ policy on declaration of interests and declare the following interests: AA is an unpaid member of XX group developing guidelines for ZZ."
We ask authors of research papers to use a revised version of the ICMJE’s unified disclosure form . The unified form can be used for several journals. Each journal, will, however, integrate the form into its processes in different ways.
Authors must disclose three types of information:
Associations with commercial entities that provided support for the work reported in the submitted manuscript (the timeframe for disclosure in this section of the form is the lifespan of the work being reported).
Associations with commercial entities that could be viewed as having an interest in the general area of the submitted manuscript (in the three years before submission of the manuscript).
Non-financial associations that may be relevant or seen as relevant to the submitted manuscript.
All authors must complete the disclosure form and send it to the corresponding author who will use the information in the forms to craft the COI statement for the paper (examples provided below). The statement but not the forms must be included with the submission. and that must be included with the initial submission. If the paper is accepted, these forms will be required and will be published alongside the article.
The statement in the manuscript should take the following format:
"Competing interests: All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/disclosure-of-interest/ and declare: no support from any organisation for the submitted work [or describe if any]; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years [or describe if any]; no other relationships or activities that could appear to have influenced the submitted work [or describe if any].”
Examples of statements:
No competing interests: "All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/disclosure-of-interest/ and declare: no support from any organisation for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work."
Grant funding for research but no other competing interest: "All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/disclosure-of-interest/ and declare: all authors had financial support from ABC Company for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work."
Mixed competing interests: "All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/disclosure-of-interest/ and declare: no support from any organisation for the submitted work; AB has received research grants and honorariums from XYZ company, BF has been paid for developing and delivering educational presentations for BBB foundation, DF does consultancy for HHH and VVV companies; no other relationships or activities that could appear to have influenced the submitted work."
Complete The BMJ 's Disclosure form . We do not need to receive signed copies of the statements regarding competing interests or the licence to publication: these are for information only. When submitting your article (or a revised version of it) you will be prompted at our online editorial office to tick two boxes , confirming that you have read and complied with our policies on competing interests and licence to publication. Please also ensure that your manuscript, whether in original or revised form, also includes your written statements of competing interests and licence to publication.
In addition to the above, all of our articles have additional requirements which should be fulfilled before submitting. For more information on any of the requirements below, please contact [email protected] .
We have produced a checklist to help authors decide whether The BMJ is the right journal for their research. If the work does not seem to fit in The BMJ , it may be better sent straight to another journal with a more specialist or local readership or a higher acceptance rate.
To learn more about the kind of research articles we give priority to, and what services we offer to authors of research, please read the editorial "Publishing your research study in the BMJ ?" . Please note that we welcome studies - even with "negative" results - as long as their research questions are important, new, and relevant to general readers and their designs are appropriate and robust.
To encourage full and transparent reporting of research we do not set fixed word count limits for research articles. Nonetheless, we ask you to make your article concise and make every word count. You will be prompted to provide the word count for the main text (excluding the abstract, references, tables, boxes, or figures) when you submit your manuscript.
Original research articles should follow the IMRaD style (introduction, methods, results, and discussion) and should include a structured abstract (see below), a structured discussion, and a succinct introduction that focuses - in no more than three paragraphs - on the background to the research question.
For an intervention study, the manuscript should include enough information about the intervention(s) and comparator(s) (even if this was usual care) for reviewers and readers to understand fully what happened in the study. To enable readers to replicate your work or implement the interventions in their own practice, please also provide any relevant detailed descriptions and materials (uploaded as one or more supplemental files, including video and audio files where appropriate). Alternatively, please provide in the manuscript URLs to openly accessible websites where these materials can be found.
Please ensure that the discussion section of your article comprises no more than a page and a half and follows this overall structure, although you do not need to signpost these elements with subheadings:
• Statement of principal findings • Strengths and weaknesses of the study • Strengths and weaknesses in relation to other studies, discussing important differences in results • Meaning of the study: possible explanations and implications for clinicians and policymakers • Unanswered questions and future research
This video gives more detailed advice on writing each section of a research paper for The BMJ .
Please ensure that the structured abstract is as complete, accurate, and clear as possible and has been approved by all authors. We may screen original research articles by reading only the abstract.
Abstracts should be 250- 300 words long: you may need up to 400 words, however, for a CONSORT or PRISMA style abstract. MEDLINE can now handle up to 600 words. Abstracts should include the following headings, but they may be modified for abstracts of clinical trials or systematic reviews and meta-analyses according to the requirements on the the CONSORT extension for abstracts and the PRISMA extension for abstracts , respectively.
• Objectives - a clear statement of the main aim of the study and the major hypothesis tested or research question posed • Design - including factors such as prospective, randomisation, blinding, placebo control, case control, crossover, criterion standards for diagnostic tests, etc. • Setting - include the level of care, eg primary, secondary; number of participating centres. Be general rather than give the name of the specific centre, but give the geographical location if this is important • Participants (instead of patients or subjects) - numbers entering and completing the study, sex, and ethnic group if appropriate. Give clear definitions of how selected, entry and exclusion criteria. • Interventions - what, how, when and for how long. This heading can be deleted if there were no interventions but should normally be included for randomised controlled trials, crossover trials, and before and after studies. • Main outcome measures - those planned in the protocol, those finally measured (if different, explain why). • Results - main results with (for quantitative studies) 95% confidence intervals and, where appropriate, the exact level of statistical significance and the number need to treat/harm. Whenever possible, state absolute rather than relative risks. • Conclusions - primary conclusions and their implications, suggesting areas for further research if appropriate. Do not go beyond the data in the article. Conclusions are important because this is often the only part that readers look at. • Trial registration - registry and number (for clinical trials and, if available, for observational studies and systematic reviews).
When writing your abstract, use the active voice but avoid "we did" or "we found". Numbers over 10 do not need spelling out at the start of sentences. p-values should always be accompanied by supporting data, and denominators should be given for percentages. Confidence intervals should be written in the format (15 to 27) within parentheses, using the word "to" rather than a hyphen. Abstracts do not need references.
We want your piece to be easy to read but also as scientifically accurate as possible. We encourage authors to review the "Statistical Analyses and Methods in the Published Literature or The SAMPL Guidelines" while preparing their manuscript.
Whenever possible, state absolute rather than relative risks. Please include in the results section of your structured abstract (and in the article's results section) the following terms, as appropriate:
For a clinical trial:
• Absolute event rates among experimental and control groups. • RRR (relative risk reduction). • NNT or NNH (number needed to treat or harm) and its 95% confidence interval (or, if the trial is of a public health intervention, number helped per 1000 or 100,000).
For a cohort study:
• Absolute event rates over time (eg 10 years) among exposed and non-exposed groups • RRR (relative risk reduction)
For a case control study:
• OR (odds ratio) for strength of association between exposure and outcome
For a study of a diagnostic test:
• Sensitivity and specificity • PPV and NPV (positive and negative predictive values)
The box stating 'what is known' and 'what this study adds' should also reflect accurately the above information. Under what this study adds, please give the one most useful summary statistic eg NNT.
Please do not use the term 'negative' to describe studies that have not found statistically significant differences, perhaps because they were too small. There will always be some uncertainty, and we hope you will be as explicit as possible in reporting what you have found in your study. Using wording such as "our results are compatible with a decrease of this much or an increase of this much" or 'this study found no effect' is more accurate and helpful to readers than "there was no effect/no difference." Please use such wording throughout the article, including the structured abstract and the box stating what the paper adds.
Provide one or more references for the statistical package(s) used to analyse the data - for example, RevMan for a systematic review. There is no need to provide a formal reference for a very widely used package that will be familiar to general readers - for example, Stata - but please say in the text which version you used.
Reporting guidelines promote clear reporting of methods and results to allow critical appraisal of the manuscript. We ask that all manuscripts be written in accordance with the appropriate reporting guideline. Please submit as supplemental material the appropriate reporting guideline checklist showing on which page of your manuscript each checklist item appears. A complete list of guidelines can be found in the website of the Equator Network . Below is the list of most often used checklists but others may apply.
For a clinical trials , use the CONSORT checklist and also include a structured abstract that follows the CONSORT extension for abstract checklist, the CONSORT flowchart and, where applicable, the appropriate CONSORT extension statements (for example, for cluster RCTs, pragmatic trials, etc.). A completed TIDieR checklist is also helpful as this helps to ensure that trial interventions are fully described in ways that are reproducible, usable by other clinicians, and clear enough for systematic reviewers and guideline writers.
For systematic reviews or meta-analysis of randomised trials and other evaluation studies, use the PRISMA checklist and flowchart and use the PRISMA structured abstract checklist when writing the structured abstract.
For studies of diagnostic accuracy , use the STARD checklist and flowchart.
For observational studies , use the STROBE checklist and any appropriate extension STROBE extensions.
For genetic risk prediction studies, use GRIPS .
For economic evaluation studies , use CHEERS .
For studies developing, validating or updating a prediction model , use TRIPOD .
For articles that include explicit statements of the quality of evidence and strength of recommendations, we prefer reporting using the GRADE system.
For studies using data from electronic health records, please use CODE-EHR .
A cover letter is your opportunity to introduce your study to the editor, highlighting the most important findings and novelty. Please also include in the letter the following information:
The BMJ is encouraging active patient and public involvement in clinical research as part of its patient partnership strategy . This is research which is "co produced" with patients, carers, or members of the public. Patient involvement in this context is not about being a research participant, answering surveys, or being an interviewee. It encompasses setting research priorities, defining research questions and outcome measures, providing input into study design and conduct, dissemination of results, and evaluation.
To support co production of research we request that authors provide a short paragraph as a subsection within the methods section of their papers entitled Patient and Public Involvement detailing how they involved the patients and the public in their research. We request this to both encourage the movement and ensure that BMJ readers can easily see whether, and if so how, patients and the public were involved in the research. If they were not involved in any way this information should be formally documented in the Patient and Public Involvement section.
As co production of research with patients and the public is relatively new we appreciate that not all authors will have involved them in their studies. We also appreciate that patient / public involvement may not be feasible or appropriate for all papers. We therefore continue to consider papers where they were not involved.
The Patient and Public Involvement section should provide a brief response to the following questions, tailored as appropriate for the study design reported:
• At what stage in the research process were patients/public first involved in the research and how? • How were the research question(s) and outcome measures developed and informed by their priorities, experience, and preferences? • How were patients/public involved in the design of this study? • How were they involved in the recruitment to and conduct of the study? • Were they asked to assess the burden of the intervention and time required to participate in the research? • How were (or will) patients and the public be involved in choosing the methods and agreeing plans for dissemination of the study results to participants and wider relevant communities? You may find this link helpful.
In addition to considering the points above we advise authors to look at guidance for best reporting of patient and public involvement as set out in the GRIPP2 reporting checklist.
If information detailing whether there was patient and public involvement, or not, is missing in the submitted manuscript we will request authors to provide it.
Where they have been involved we consider it good practice for authors to name and thank them in the contributorship statement after seeking their permission to do so; and to clearly identify them as patient/public contributors. When they have contributed substantially and meet authorship criteria they should be invited to coauthor the manuscript.
Links to selected examples of Patient and Public Involvement statements in published BMJ research papers showing patient and carer involvement at various stages of the research process.
Comparison of the two most commonly used treatments for pyoderma gangrenosum: results of the STOP GAP randomised controlled trial
Evidence based community mobilization for dengue prevention in Nicaragua and Mexico
Computerised cognitive behaviour therapy (cCBT) as treatment for depression in primary care (REEACT trial): large scale pragmatic randomised controlled trial .
Real world effectiveness of warfarin among ischemic stroke patients with atrial fibrillation: observational analysis from Patient-Centered Research into Outcomes Stroke Patients Prefer and Effectiveness Research (PROSPER) study.
Example PPI statements to adapt for use in a paper
Examples to guide the wording for PPI statements
We require a data sharing statement for all research papers. For papers that do not report a trial, we do not require that the authors agree to share the data, just that they say whether they will.
For reports of clinical trials, we ask that the authors commit to making the relevant anonymised patient level data available on reasonable request (see editorial ). This policy applies to any research article that reports the main endpoints of a randomised controlled trial of one or more drugs or medical devices in current use, whether or not the trial was funded by industry.
"Relevant data" encompasses all anonymised data on individual patients on which the analysis, results, and conclusions reported in the paper are based. As for "reasonable request," The BMJ is not in a position to adjudicate, but we will expect requesters to submit a protocol for their re-analysis to the authors and to commit to making their results public. We will encourage those requesting data to send a rapid response to thebmj.com, describing what they are looking for. If the request is refused we will ask the authors of the paper to explain why.
In addition, we will follow the new ICMJE data sharing policy that goes into place on July 1, 2018 (see editorial ): manuscripts submitted to ICMJE journals that report the results of clinical trials must contain a data sharing statement that indicates whether individual de-identified participant data (including data dictionaries) will be shared; what data in particular will be shared; whether additional, related documents will be available (study protocol, statistical analysis plan, etc); when the data will become available and for how long; by what access criteria data will be shared (including with whom, for what types of analyses, and by what mechanism). Clinical trials that begin enrolling participants on or after January 1, 2019 must also include a data sharing plan in the trial’s registration. If the data sharing plan changes after registration this should be reflected in the statement submitted and published with the manuscript, and updated in the registry record.
We encourage authors of all research articles in The BMJ to link their articles to the raw data from their studies. For clinical trials, we require data sharing on request as a minimum and- if authors of such trials are willing to go further and share the data openly, so much the better. The BMJ has partnered with the Dryad digital repository datadryad.org to make open deposition easy and to allow direct linkage by doi from the dataset to The BMJ 's article and back (for The BMJ 's articles' datasets see here ).
Data requesters should do the following: • Submit a rapid response to the paper and email the corresponding author for the paper to request the relevant data. • Be prepared to provide the authors of the paper a detailed protocol for your proposed study, and to supply information about the funding and resources you have to carry out the study. • If appropriate, invite the original author[s] to participate in the re-analysis. • If a month elapses without a response from the authors, please email the head of research for The BMJ (presently [email protected] ) and cc [email protected] . • The BMJ will assess the request and if appropriate we will encourage the authors or their institution to share the data, although we are not in a position to compel data release or broker agreements. Our role is limited to making the request process public, and all correspondence related to the request may be made public through rapid responses to the paper.
The BMJ requires that research data be disaggregated by sex and gender. If that is not possible, please include a detailed explanation of the reasons for this, and mention it as a limitation in the discussion section.
Ethics approval
All research studies published in The BMJ should be morally acceptable, and must follow the World Medical Association's Declaration of Helsinki . To ensure this, we aim to appraise the ethical aspects of any submitted work that involves human participants, whatever descriptive label is given to that work including research, audit, and sometimes debate. This policy also applies on the very rare occasions that we publish work done with animal participants. The manuscript must include a statement that the study obtained ethics approval (or a statement that it was not required), including the name of the ethics committee(s) or institutional review board(s), the number/ID of the approval(s), and a statement that participants gave informed consent before taking part.
Transparency statement
Please include in your manuscript a transparency declaration : a statement that the lead author (the manuscript's guarantor) affirms that the manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as originally planned (and, if relevant, registered) have been explained.
The BMJ is committed to making the editorial process transparent and ethical. The BMJ ’s transparency policies are accessible from this link .
Role of the funding source
Please include in the manuscript a statement giving the details of all sources of funding for the study. As appropriate, the statement must include a description of the role of the study sponsor(s) or funder(s), if any, in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; and in the decision to submit the article for publication. In addition, the statement must confirm the independence of researchers from funders and that all authors, external and internal, had full access to all of the data (including statistical reports and tables) in the study and can take responsibility for the integrity of the data and the accuracy of the data analysis is also required.
If you are submitting an original article reporting an industry sponsored clinical trial, postmarketing study, or other observational study please follow the guidelines on good publication practice (GPP2) and on properly reporting the role of professional medical writers. Another resource, the Authors' Submission Toolkit: A practical guide to getting your research published summarises general tips and best practices to increase awareness of journals' editorial requirements, how to choose the right journal, submission processes, publication ethics, peer review, and effective communication with editors - much of which has traditionally been seen as mysterious to authors.
The BMJ will not consider for publication any study that is partly or wholly funded by the tobacco industry, as explained in this editorial .
Patient and Public Involvement statement
Within the Methods section of your paper, please state if and how patients and the public were involved in the research you are describing. For more information, please see the specific guidance on mandatory reporting of patient and public involvement above. If patients and the public were not involved this information should be formally documented in the Patient and Public Involvement statement.
Dissemination to participants and related patient and public communities
For accepted papers we will ask you to confirm when and how the results of your study were (or will be) sent to research participants and whether they are also being sent to relevant patient and public communities, as applicable. If you have not disseminated and have no plans to do so, please state why.
Please produce a box offering a thumbnail sketch of what your article adds to the literature. The box should be divided into two short sections, each with 1-3 short sentences.
In two or three single sentence bullet points, please summarise the state of scientific knowledge on this topicbefore you did your study, and why this study needed to be done. Be clear and specific, not vague.
In one or two single sentence bullet points, give a simple answer to the question “What do we now know as a result of this study that we did not know before?” Be brief, succinct, specific, and accurate. For example: "Our study suggests that tea drinking has no overall benefit in depression." You might use the last sentence to summarise any implications for practice, research, policy, or public health. For example, your study might have asked and answered a new question (one whose relevance has only recently become clear); contradicted a belief, dogma, or previous evidence provided a new perspective on something that is already known in general; or provided evidence of higher methodological quality for a message that is already known. DO not make statements that are not directly supported by your data.
Trial registration
In accordance with the International Committee of Medical Journal Editors' Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals , The BMJ will not consider reports of clinical trials unless they were registered prospectively before recruitment of any participants. This policy on prospective registration applies to trials that started after 1 July 2005; for older trials retrospective registration will be acceptable, but only if completed before submission of the manuscript to the journal. The trial registration number and name of register should be included as the last line of the structured abstract. The BMJ accepts registration in any registry that is a primary register of the WHO International Clinical Trials Registry Platform (ICTRP) or in ClinicalTrials.gov , which is a data provider to the WHO ICTRP.
In your submission, please include details about registration: registry, date registered, affirmation that registration was prospective before enrolling the first patient (if applicable) and registry number. The BMJ relies on information contained in trial registries. If authors believe that information in the registry is incorrect they should make their case to registry officials.
Eligible trials have been defined by ICMJE since 1 July 2008 as trials "where human participants are prospectively assigned to one or more health-related interventions (including health services and behavioural interventions) to evaluate the effects on health outcomes," and before that were defined more narrowly as trials "where human participants are prospectively assigned to investigate the cause and effect relationship between a medical intervention and health outcome." The ICMJE further states that, "Some trials assign healthcare providers, rather than patients, to intervention and comparison/control groups. If the purpose of the trial is to examine the effect of the provider intervention on the health outcomes of the providers' patients, then investigators should register the trial. If the purpose is to examine the effect only on the providers (for example, provider knowledge or attitudes), then registration is not necessary." We will take these definitions into account when evaluating if trials were adequately registered.
The BMJ does not consider posting of protocols and results in clinical trial registries to be prior publication. We also will consider research articles that have been posted on preprint servers, provided this is clearly disclosed on submission of the paper.
The BMJ encourages but does not require registration of protocols and posting of results in publicly accessible registries for studies that are not clinical trials if they involve human participants, particularly observational studies . If the study was registered, please provide the registration details, explaining whether the study was registered before data acquisition or analysis began.
The BMJ expects authors of clinical trials to report their findings in accordance with the outcomes listed in the trial registry. Outcomes that were not pre-specified in the registration should be identified as such in the text of the paper and in any tables. All registered outcomes should be described in the BMJ paper. If results for any outcomes will be or have been reported in another publication this should be made clear to readers. The timing and reasons for any changes in registered outcomes should also be disclosed.
The BMJ requires authors of clinical trials to upload a protocol for their study. This protocol will be published alongside other materials if the article is accepted. Any discrepancies between the protocol-specified outcomes and those listed in the trial registry or reported in the paper should be explained in the paper. In cases where pre-specified outcomes differ between the trial registration and the protocol, our policy is to consider the outcomes listed in the registry as pre-specified. Outcomes listed in the protocol but not the trial registry can be reported in the paper, but should be identified as post-hoc outcomes. Protocols vary in completeness and content. There are often multiple versions of a protocol and the timing of decisions about outcomes in relation to the onset of a trial cannot easily be determined. This is in contrast to trial registries, where date stamps are reliable and can be easily verified by readers.Trial registry entries should be updated if new outcomes are added or existing ones deleted, promoted, or demoted.
The BMJ requires authors of clinical trials to upload a statistical analysis plan (SAP) for their study. The SAP will be published alongside other materials if the article is accepted. A SAP provides more detailed information about statistical analysis than a protocol, including detailed descriptions of procedures used to execute the analyses. Please follow the guidance on producing a SAP contained in the table of this document: https://jamanetwork.com/journals/jama/fullarticle/2666509
Research papers in The BMJ are published with open access. Moreover, The BMJ immediately fulfils the requirements of the US National Institutes of Health, the UK Medical Research Council, the Wellcome Trust, and other funding bodies by making the full text of publicly funded research freely available to all on bmj.com and sending it directly to PubMed Central, the National Library of Medicine's full text archive. The BMJ occasionally publishes as open access other types of (non-research) articles arising from work funded by a funder who mandates open access publication.
Open access articles may be reused according to the relevant Creative Commons licence. The BMJ 's default licence for open access publication of research is the Creative Commons Attribution Non Commercial licence (CC BY-NC 4.0) . But where the funder requires it the author can select the Creative Commons Attribution (CC BY 4.0) licence during the submission process (funders who mandate CC BY include the Wellcome Trust, RCUK, and MRC).
To support this, we ask authors to pay an open access article processing charge - you can find our author charges for open access here . We can offer discounts and waivers for authors who cannot pay. Consideration of the paper is not related to whether authors can or cannot pay the fee. We will ask for the fee only once we have accepted a paper, and we will send an invoice only once authors tell us (via [email protected] ) they can claim the fee. Seeking and processing fees will not delay editing or publication. Please do not contact editors about open access fees: neither editors nor reviewers will know whether a fee is payable, and administrative staff will handle payments and all associated correspondence. For non-research articles published with open access we will ask authors to pay the open access fee. We do not offer refunds for Open Access once articles have been published. For further information, contact [email protected] .
A number of institutions have open access institutional memberships with BMJ (the publishing group), which either cover the whole cost of open access publishing for authors at participating institutions or allow authors to receive a discount on the article processing charge. For a list of member institutions and their policies on how to receive a discount or to publish free of charge, please visit http://journals.bmj.com/site/authors/openaccess.xhtml
For articles not published with open access, The BMJ 's publication licence allows each author to post their article's URL (provided above) on either their own or their employer's website, thereby giving users free access to the full text of the article on bmj.com. Authors will need to use the toll free link to ensure visitors have free access to the article. Alternatively, authors can post the full text of their published article on their own website or their employer's website.
For additional information, please see the section of instructions to authors on copyright, open access, and permission to reuse .
The BMJ will pilot a small number of living systematic reviews
Duration : We will typically host a living systematic review which is live for up to 2 years after initial publication. The triggers for updates, and their frequency, will be decided with authors on a case by case basis. Communication : The title will reflect the living nature of the review and the most recent update will become the default publication on bmj.com. Reviews will have a single digital object identifier (DOI) to keep the information in one place. However, previous versions will remain available as data supplements. An updates table will be included in the review to make tracking the history of the review easier and to signal planned changes. Updates will be flagged on bmj.com, including in rapid responses. They will also be communicated to third parties including PubMed and PubMedCentral. Updates : Updates should be submitted as a “track changes” version of the final MIcrosoft Word version of the previous iteration of the review. A clean version should also be submitted via the ScholarOne manuscript system. Subsequent internal or external peer review reports will be added to the pre-publication history tab on bmj.com with each version of the paper. The approach to any authorship changes should be negotiated before the first version of the paper is published. Resources : The usual BMJ article open access processing fee will be charged for the initial version of the review and an additional fee will be added to cover the cost of up to three updates per year (£2000 per update). After the first year the price may be revised based on the scope of the revisions and the work done on each one.
Preliminary reporting guidance for living reviews
COVER LETTER: This should explain and defend the need for the review to be “living.” Briefly describe other extant reviews, in particular any other living systematic reviews that have recently been published. The cover letter should acknowledge the authors’ acceptance of the following special conditions that apply to living reviews: 1) the need to provide current conflict of interest declarations or updates for all authors at each revision; 2) the single DOI for the paper and updates; agreement that open access fees cannot be waived for living reviews and that additional fees apply to cover the extra work of producing and maintaining living reviews.
TITLE: The phrase “living systematic review” should appear in the title. If additional terms apply, those may be included as appropriate (e.g. “network meta-analysis,” “meta-analysis,” “critical appraisal,” etc.).
ABSTRACT: The abstract should include: 1) A statement of the research question or objective, including a statement that one objective is to provide regular updates and keep the review live. 2) The rationale for a living systematic review should be described, e.g. rapidly evolving evidence base, anticipated impact on policy or practice, etc. 3) A “Readers’ note” at the end of the abstract that provides information about the version of the paper, the date it went live, and gives notice of planned updates. For example: “Readers’ note: This article is a living systematic review that will be updated periodically over the next 2 years to reflect emerging evidence. This version is update XXX of the original article published XXXXXX (give BMJ DOI), and previous updates can be found as data supplements (give link). When citing this paper please consider adding the version number and date of access for clarity.”
MAIN PAPER: Please address the following matters in the appropriate section of the paper: Introduction: -- Include the information required in the abstract (see above paragraph) at the end of the introduction section. -- In updates, consider including a short paragraph that describes how the living review has evolved. For example, what are the key developments since the previous version of the review, and what developments might be expected? Methods -- Mention and include a reference to any published or publicly available protocol for this review. If not registered, consider registering the review. -- Describe the methods that will be used to keep the review living, including the processes that will be used to search for new evidence, anticipated triggers for updates, and the circumstances under which the review might end before the 2 year time limit for BMJ Living Reviews. -- In updated versions of the review, make clear when and why any methods have evolved over time. If these descriptions are lengthy or complex, consider doing this in a table that can be included in an appendix or supplemental file. Such a table will ideally describe important changes to the review protocol, statistical analyses, or other aspects of the review, along with the dates of these changes. -- A table at the end of the discussion section might be used to highlight new evidence that was not included in the review. Results -- Clearly state the updated dates of the search. Discussion -- Consider additional subheadings to separate, e.g. What remain the important findings so far? Versus what are the main new findings to highlight? -- Consider additional table updates to this article. This will make clear historical and anticipated change. Columns trigger, date and action. Declaration of competing interests -- All authors must complete the ICMJE Competing Interests form with the initial submission. At each revision, we will ask the corresponding author to state whether there have been any changes to competing interests among any of the existing authors. If there are changes or if new authors have been added, the corresponding author is responsible for ensuring the this information is up to date. Otherwise there will be no change to the declaration of interests. Supplementary files -- Previous versions of the paper
Please contact Dr. Elizabeth Loder ( [email protected] ) with any questions.
You may submit the following materials as supplemental files if you think they will help the authors and reviewers make a decision or readers better understand your study:
Original raw data if you think they will help our reviewers (and maybe readers), or if we specifically request them. Please note our policy on data sharing, explained above.
Video and audio files that will add educational value to your article, for example by explaining the intervention in a trial.
A video abstract that summarizes your findings and that will be posted on bmj.com with your paper. You can find additional information about video abstracts here and here .
Public and patient involvement materials used in your research.
Copies of any non-standard questionnaires and assessment schedules used in the research.
Copies of patient information sheets used to obtain informed consent for the study or to comprise or deliver the intervention in a clinical trial.
Copies of closely related articles you have published (this is particularly important when details of the study methods are published elsewhere).
Copies of any previous reviewers' reports on this article . We appreciate that authors may have tried other journals before sending their work to The BMJ , and find it helpful if you let us know how you have responded to previous reviewers' comments.
We are willing to consider papers that present new or updated research reporting guidelines, but only if the guideline pertains to a study type that we publish in The BMJ. The checklist itself must be included as part of the paper. We prefer to be the only journal publishing the guideline, but under some circumstances we will consider co-publication with up to two other journals. For an example of how to format a reporting guideline to appear in our research methods and reporting section, see http://www.bmj.com/content/346/bmj.f1049.full.pdf+html .
Word count We do not set fixed word count limits for RMR articles. Nonetheless, we ask you to make your article concise and make every word count. For some submissions this might be published in full on bmj.com with a shorter version in the print BMJ
Overall structure Research Methods and Reporting should have the following elements:
Title and standfirst A short title is followed by an 100-150 word italicised single sentence (the standfirst) which encapsulates the article’s central message.
Introduction Articles should begin with a brief paragraph that captures readers’ attention and explains the aim of the piece.
Text The body of the text should be broken up under subheadings that provide a logical narrative structure. Avoid acronyms and abbreviations unless they are universally recognised e.g. DNA. The evidence on which key statements are based should be explicit and referenced, and the strength of the evidence (published trials, systematic reviews, observational studies, expert opinion etc.) addressed.
Boxes, tables and figures Include tables, boxes, or illustrations (clinical photographs, imaging, line drawings, and figures) to enhance the text and add to or substantiate key points made in the body of the article. Figures may be in color. Worked out examples that use specific methods under discussion can be included as additional boxes. If appropriate, include a box of linked information such as website urls for those who want to pursue the subject in more depth.
Web extras We may be able to publish on bmj.com some additional boxes, figures, and references (in a separate reference list numbered w1, w2,w3, etc. and marked as such in the main text of the article). Also may include suggestions for linked podcasts or video clips, as appropriate.
Contributors and sources We ask for a 100-150 word supplementary paragraph (excluded from word count) to explain the article’s provenance. It should include the relevant experience and expertise of each author, his or her contribution to the paper, and the sources of information used to prepare it. One author must be nominated as the guarantor of the article. Include a statement of sources and selection criteria.
Summary points Include up to four sentences, in the form of bullet points, highlighting the article's main points.
References Must be in Vancouver style and should be kept to a minimum; ideally no more than 20.
“Analysis” is a distinct article type at The BMJ , and differs from other sections such as research, education, editorials, and opinion. A great analysis article makes an argument and supports it with data. It has academic heft yet is a journalistic read. Academic heft means the argument is scholarly, evidence-based, and supported by data. Journalistic read means the article is written in clear, active language, avoids technical jargon, and is pitched to our international audience of general medical readers.
We receive many manuscripts that are not a good fit for the analysis section. We generally do not consider:
• Case studies or articles mostly concerning the author’s writing about their own work • Manuscripts containing primary research data (such papers should be submitted as research) • Narrative reviews • Articles presenting a new hypothesis
If you are unsure if your work is suitable for The BMJ 's analysis section we are willing to consider succinct pre-submission inquiries, please complete the form in this link and await a response from Jocalyn Clark, Head of Scholarly Comment, or one of the analysis editors.
We recommend looking at this Analysis article template and using it as a basis for your work before considering submission.
Word count and style The BMJ has an international readership that includes policy makers, health professionals, and doctors of all disciplines. Authors are advised to keep this readership in mind and to write their article for the non-expert. It’s important to avoid jargon. Specialised terminology and references to organisations or practices that are specific to one country need to be explained. Clear writing and active language are essential. Analysis papers should be 2000 words with 20 references and up to 3 non-text items (box, figure, or table).
Overall structure The manuscript should have the following elements:
Title and standfirst A short title is followed by an italicised single sentence (the standfirst), which encapsulates the article’s central message.
Introduction Articles should begin with a brief paragraph that captures readers’ attention and explains the aim of the piece and “why now”.
Text The body of the text should be broken up under sub-headings that provide a logical narrative structure. Avoid acronyms and abbreviations unless they are universally recognised e.g. DNA. The evidence on which key statements are based should be explicit and referenced, and the strength of the evidence (published trials, systematic reviews, observational studies, expert opinion, etc.) made clear. Articles should present a balanced, even-handed look at the evidence rather than selectively citing evidence that supports a particular view.
Boxes, tables and figures These should extend and substantiate points made in the body of the paper. Words in boxes and tables are excluded from the word count of the body of the text but the additional material should be concise.
Key messages box This should be at the end of the article and include 3-4 points summing up the main conclusions. When submitting your article please enter your key messages when prompted to enter the abstract.
Contributors and sources We ask for a 100-150 word supplementary paragraph (excluded from word count) to explain the article’s provenance. It should include the relevant experience and expertise of each author, his or her contribution to the paper, and the sources of information used to prepare it. One author must be nominated as the guarantor of the article.You are welcome to invite co-authors to work with you on the article. We suggest including 2-3 co-authors with different locations and perspectives to help ensure articles are international in scope and accessible to our broad readership online and in print, and we encourage diversity in co-authorship including gender balance and the inclusion of colleagues from low and middle income countries.
Report of patient involvement As The BMJ is seeking to advance partnership with patients, we also ask authors to seek their input into articles wherever relevant, and document their involvement as patient contributors or coauthors.
Conflicts of Interest All authors should read our competing interests policy and include relevant declarations for all authors in their manuscript. We seek to publish independent Scholarly Comment and require competing interests to be declared upon submission. Where a competing interest exists that you think might disqualify an author from contributing, please discuss it with a BMJ editor before writing the article.
Licence We require the manuscript to include the following statement:
Peer review The BMJ has fully open peer review for analysis articles. This means that every accepted analysis article submitted from February 2016 onwards will have its prepublication history posted alongside it on thebmj.com. This prepublication history comprises all previous versions of the manuscript, the report from the manuscript committee meeting, the reviewers’ signed comments, and the authors’ responses to all the comments from reviewers and editors. Authors are welcome to suggest names of suitable reviewers, including patient reviewers.
Analysis articles progress through several stages:
• All submissions are read in full by one or more members of the editorial team. • Articles that pass the initial editorial screen are sent for external peer review. • Articles are then discussed at a regular analysis committee meeting where editors make one of three decisions: reject; major revision; or minor revision with aim to accept.
In most cases we will publish the prepublication history alongside an accepted analysis article. This prepublication history comprises all previous versions of the manuscript, the report from the manuscript committee meeting, the reviewers’ comments, and the authors’ responses to all the comments from reviewers and editors. In rare instances we may determine after careful consideration that we should not make certain portions of the prepublication record publicly available. For example, in cases of stigmatised illnesses we seek to protect the confidentiality of reviewers who have these illnesses. In other instances there may be legal or regulatory considerations that make it inadvisable or impermissible to make available certain parts of the prepublication record. In all instances in which we have determined that elements of the prepublication record should not be made publicly available, we expect that authors will respect these decisions and also will not share this information.
Rapid responses are electronic letters to the editor and offer readers a way to interact with our content. Sometimes responses may be critical of an article. We believe that authors have an academic duty to respond to substantive criticism of their work and we expect authors to post their own rapid responses on bmj.com in reply to any such substantive comments. Editors may send reminders about this.
The BMJ publishes different types of educational articles to engage and challenge a range of postgraduate doctors and clinical researchers internationally. We strive to publish articles that are original in their content and/or presentation, and cannot be found elsewhere or in textbooks. We prioritise topics and situations that are common or have serious consequences, have international appeal, and that interest a variety of doctors, including GPs and specialists.
We encourage authors to write in teams, including those from other specialties, professions, and countries. We ask that one author is routed in the clinical environment of the intended reader. We encourage authors to write in plain English, to be clear about where there is uncertainty, and to include numbers and phrases where possible that will help doctors in conversation with their patients.
Our educational articles are shaped by two initiatives:
• We believe that financial interests can distort education articles and we minimise or exclude authors who we judge have such a conflict.
• We believe that patient involvement strengthens content. We encourage authors to seek input from patients either to inform the scope, develop the content, contribute to, or co-author articles. For help with this, please read our guidance on what we mean by patient involvement and co-production . Author guidance for Education articles can be found here.
We receive more articles and suggestions than we can publish. We require all authors to contact us before submitting a manuscript to us. Send us your proposal using our Education Article Proposal Form , together with your completed Declaration of Financial Interests .
The proposal form will guide you through the following questions:
• What is your idea? • Can you sum up the aim of your article in a sentence? • Why is the topic important to The BMJ 's readers? • What is the prevalence of the symptom/condition/situation you wish to write about? • Why cover it now? Has something new happened? • What has The BMJ 's Education section covered on this topic in the last five years? What will your contribution add? • Can you provide the key evidence/references you might use? • Why are your writing team well placed to cover the topic? • Have you thought about what a patient would say about your idea?
Authorship Education articles can have can have up to four authors. One author should be from the relevant specialty or setting, unless agreed otherwise. For example, if the article discusses presentation to the emergency department one author should be an emergency care doctor. All authors should meet authorship criteria . We welcome authors or contributions from allied health professions and patient authors, and actively encourage authors from a primary care background.
Competing interests The BMJ will not consider authors with financial interests when writing Education articles. It is important that we understand the financial interests of every author, and can judge to what extent we believe that they may be relevant to the article that you propose. We do not publish content from authors who we judge have relevant financial ties to the industry (excluding State of the Art reviews, Therapeutics articles, and Summaries of NICE Guidelines). The relevance of declared interests are judged by the BMJ team. This applies to every author. Any additional authors and their financial interests must be discussed and agreed with the commissioning editor before the article is submitted.
Patient involvement As part of our drive to co-produce our content with patients we ask that you seek patient input into articles at the planning stage. We believe that their experience and perspectives will make articles more useful for doctors in their quest to help improve patients well being and outcomes.
We ask all authors to what extent patients have been involved in their article and how their involvement changed the article. We ask that all writing encourages honesty and partnership with patients. Where uncertainty exists, share it. Where data exists present the numbers in a way that can be shared with the patient (use absolute numbers, natural frequencies, and graphics where you can). Use language that empowers patients to make the right choices for them in their situation (write that a doctor should/could offer a test, rather than should do a test).
When patients are involved in the manuscript, we ask for their consent. We have two types of consent forms for BMJ education articles:
• A patient consent form is required if any anonymised patient information is included in the review. Consent is needed for images even if the patients are not identifiable for example, in X-rays and histology slides, and for patients’ stories/vignettes even if details are anonymised.
• A patient contributor form is required for any patients who are named within the review, for example, patient co-authors, patient contributors or named authors of patient stories.
We want our readers to have the ability to share decisions with their patients and make clear for them the degree of certainty ( or lack of it) about a potential course of action. We therefore ask that, in addition to the format and instructions detailed below for the specific Education article that you are writing, you follow these recommendations:
• Consider including in your manuscript a box explaining your strategy to search for evidence. It should include a search date, the sources searched, and brief inclusion criteria. • Clearly distinguish suggestions made based on your experience, standard practice, guidelines, and evidence. • Provide specifics about the evidence you discuss. For example, for key statements, please say: "A large, well conducted, randomised controlled trial showed INSERT number [CI] and or p value". "The findings of a small case series suggest...". “A subgroup analysis found…”. etc. • Use absolute numbers or explain why you have not used them. • Consider how these numbers can be communicated by the clinician read to their patient in a clear way. • Where evidence is lacking or of poor quality make this clear. • Write about known and unknown benefits and harms.
"What you need to know" box . No more than three bullet points for practice articles and five for clinical updates encapsulating the specific take home messages from this article.
"How patients were involved in the creation of this article" box. Please include: Which patients were asked (e.g. patient advocates, networked patient communities and organisations, patients in your clinic etc). What they said (e.g. include more practical advice on how to inject insulin.) How you changed your article as a result (e.g. we included a box to address this.)
"Education into practice" box . Include two to three bullet points about how a reader might at an individual or organisational level improve their practice (e.g. do you offer lifestyle advice to all patients with newly diagnosed hypertension?)
At least one other box or table and at least one figure or image that complement the text of the article.
We accept pitches for the following article types. Once our editors have made a decision to encourage a pitch, we will provde authors will a full, detailed set of instructions on how best to format your content.
These articles provide an up-to-date overview of a clinical condition. The content should be evidence based, aimed at non-specialists and have international appeal. It should include a broad update of recent developments (from the past 1-2 years) and their likely clinical applications in primary/community and secondary/hospital care. | 1,800 words, maximum of 40 references | |
These are practical, often problem-based articles. They should help clinicians who are not specialists in a particular field know “how to” to approach a problem, diagnosis, or management better. | 1,600 words and 20 references | |
This series highlights conditions that are often missed at first presentation in general practice or the emergency department. For the condition in question, provide evidence that the condition may be misdiagnosed or that diagnosis may be delayed and that timely recognition will benefit the patient. The condition should be reasonably common (likely to present at least once a year to a full-time primary care practitioner) or is serious and delayed diagnosis is likely to worsen prognosis. The condition should have easily defined diagnostic features and/or tests with known predictive characteristics. | 1,600 words and 20 references | |
These articles describe how clinicians might use a single consultation to tackle a common scenario in primary care. Articles must address a tightly framed issue: for example how to explore a new symptom (e.g. tingling fingers), explain a diagnosis of a condition (e.g. Parkinson's disease, or an aspect of its management) or act in an urgent situation, such as on receipt of a high INR reading. | 1,000 words and 10 references | |
The Sustainable Practice series outlines tangible actions that clinicians can undertake within their clinical practice to promote sustainable healthcare. System-level changes can be incorporated, but it is important to primarily focus the suggested actions at the individual level. Sustainable Practice pieces are short articles with a structured format. Sustainable Practice articles usually have one to two authors. We encourage patient and public involvement, so consider co-production, co-authoring, or seeking patient involvement in the early stages such as reviewing a manuscript draft. If you think you have an idea that could work for this series, please fill out the . Please note that this is a separate form from the main Education article proposal form. | 400-700 words | |
This is a series led, and edited and written by patients and their carers and contain messages that are thought provoking, and challenging for readers of , along the lines of "What I wish you [ ’s audience] knew, and why." Please suggest any articles of this type directly to our patient editor, Emma Doble ( ). | Around 650 words, including the summary box at the end of each piece, called “What You Need To Know.” Find out more about the WYPIT submission process . | |
These article types are solely commissioned by our editors. | ||
| We will only publish articles authored by people free from financial interests that we consider to be relevant, which is why we ask all authors to complete our online competing interests form before submission. No more than two authors can write each Minerva Picture article. Minerva Picture articles with the following characteristics are usually accepted because they lack educational value for general readers: Before we can consider your article, we need:
| 150 words |
| Endgames articles are quizzes based on genuine clinical scenarios. The difficulty of the questions should reflect knowledge needed for postgraduate exams. Endgames also offer doctors who have passed postgraduate exams the chance to test their knowledge for continuing medical education. Please focus on standard diagnosis and management and cite major guidelines if they exist (or evidence if guidelines do not exist.) Endgames is not the place to discuss or debate various management strategies. We will only publish articles authored by people free from financial interests that we consider to be relevant. Please ensure that each potential author has completed the before submission. We will not consider a paper until we have reviewed and approved competing interests declaration forms from each author. Before we can consider your article, we also need to see written consent from every patient, parent, or next of kin, regardless of whether the patient can be identified from the picture. This must be in the form of a and must be included when you submit your article. Please do not plagiarise content. Avoid duplication of large paragraphs of text from textbooks or journals. Please provide a and attach it to your submission. • A 50 word learning point as a take home message for readers Please complete the . We will not consider your paper until we have reviewed and approved competing interests declaration forms from each author. A must be included when you submit your article. Please write your paper within our and submit it to our . | 150 word vignette (case history) section and 200 word answer section. See template for more details. |
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| BMJ editorials are scholarly, balanced, and evidence based. All substantive comments must be underpinned by recent best evidence. We reserve strong opinions for our Opinion columns. Editorials usually respond to something topical, discuss why it matters, and call for some kind of action. They should be of international interest to any or all of the following: patients, clinicians, researchers, policy makers, and guideline developers. We particularly encourage co-production of editorials with patients, patient leaders, or patient advocates. If co-authorship isn't possible please consider asking a patient to review an early draft, and acknowledge their contribution in a statement at the end. Editorials usually have 1-3 authors, and must not have more than four. Five authors are allowed only if the extra author is a patient. All authors must be cleared of relevant competing interests by the editorials editor before submission. Failure to secure clearance may jeopardise the publication of your editorial. We no longer consider clinical editorials by authors with relevant financial ties to commercial companies. We do not allow authors to editorialise their own work. Editorials do not carry original data, or personal experience/stories. Please write clearly for generalists with little specialist knowledge of your topic (such as primary care doctors, doctors in training, policy makers), and for an international audience. References should be in Vancouver style. If there are six or fewer authors cite all; if more than six please give the first six and et al. Avoid using superscript for references. Please do not use endnotes or footnotes. Editorials must include a title page giving all authors' names, addresses, email addresses, contact numbers, and job titles. | Up to 800 words long, with 12-20 references. |
| Rapid responses are electronic letters to the editor. Our weekly letters are edited selections of posted rapid responses and are indexed in PubMed. Rapid responses are not indexed in PubMed but they have their own URL and are retrievable in an advanced search of thebmj.com in perpetuity. Thus a rapid response is published with its first appearance online. Use search on bmj.com to find the article to which you are responding, and then follow the link at the top of the page, marked "Respond to this article." This is the only way to submit a letter to : all letters that appear in the printed issue of and on bmj.com arrived as rapid responses initially. | n/a |
| The best personal view pieces make a strong, novel, and well argued point. They are also often topical, insightful, and attention grabbing. We publish anonymous personal view articles only by special arrangement when it would be impossible for the article to appear with the author's name. Accepted articles are all published online initially on , but may not be published in print. Please submit online at . We cannot promise publication before the piece is submitted. | 600 words and 10 references |
| BMJ Opinion provides comment and opinion written by The BMJ's international community of readers, authors, and editors. We welcome submissions for consideration. Your article should be about medicine, healthcare, publishing, or an issue that will interest doctors and other healthcare professionals. Writing should be clear, compelling, and appeal to our international readership. The best pieces make a single topical point. All opinion articles appear online and are indexed in PubMed. Please submit via email at . | 650-800 words |
| If you have an idea for an article about doctors' careers, please pitch it to us by emailing Tom Moberly ( ). Send a few sentences explaining what you’d like to write about, how you’d like to cover the topic, and what you think readers would gain from the article you are proposing. If we like your idea we will contact you to discuss how we would like to proceed. | n/a |
| Clinical Opinion articles are short 300-500 word articles that appear online. The aim of these articles is to make readers think but they must also convey your own personal opinion on a topic. They evolved to fill a gap in the print version of . Now, all accepted submissions are published online on the website. Some are selected to appear in print on the Education pages but we cannot guarantee this. When writing, please consider the following : We welcome submissions on topics such as: As well as the article we need you to send us a short biography (a sentence or two). We also ask all authors to submit a competing interests statement, even if there's nothing to declare. Here's more on this ( ). Please could you include your twitter handle if you have one. Finally, please could you also send a photo of yourself to go online with the article. Please note that your article may be sent for peer review. Please also note that BMJ Clinical Opinion (previously Fillers) and BMJ Opinion articles are not indexed in PubMed. Please submit online at . | 300-500 words |
| . We welcome obituaries for doctors with a connection to the UK within a year of their death. We assume that material is sent exclusively to us, and we publish the full versions we receive on bmj.com. We produce the short obituaries in the print issue from these full versions; these usually appear with a time lag of several weeks. Obituaries include : the last position held, date of birth, place and year of qualification, postgraduate qualifications if applicable, and date and cause of death. Pictures should be sent as high -resolution images electronically or as photographs. We do not accept obituaries sent by post, and neither do we accept handwritten obituaries. Please include a postal address if you want us to send one a copy of the relevant print issue to the families of the deceased (additional copies will have to be purchased from ). We also need the name of the author(s) of the obituary. NB: Please do not use abbreviations. We generally commission the full page obituaries for the print issue of The BMJ from professional writers: these are usually about doctors and are published no more than three months after death. We regret that we cannot provide individual progress updates - please check to find out whether your submission has been published. | Around 150 words |
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Milind s. tullu.
Department of Pediatrics, Seth G.S. Medical College and KEM Hospital, Parel, Mumbai, Maharashtra, India
This article deals with formulating a suitable title and an appropriate abstract for an original research paper. The “title” and the “abstract” are the “initial impressions” of a research article, and hence they need to be drafted correctly, accurately, carefully, and meticulously. Often both of these are drafted after the full manuscript is ready. Most readers read only the title and the abstract of a research paper and very few will go on to read the full paper. The title and the abstract are the most important parts of a research paper and should be pleasant to read. The “title” should be descriptive, direct, accurate, appropriate, interesting, concise, precise, unique, and should not be misleading. The “abstract” needs to be simple, specific, clear, unbiased, honest, concise, precise, stand-alone, complete, scholarly, (preferably) structured, and should not be misrepresentative. The abstract should be consistent with the main text of the paper, especially after a revision is made to the paper and should include the key message prominently. It is very important to include the most important words and terms (the “keywords”) in the title and the abstract for appropriate indexing purpose and for retrieval from the search engines and scientific databases. Such keywords should be listed after the abstract. One must adhere to the instructions laid down by the target journal with regard to the style and number of words permitted for the title and the abstract.
This article deals with drafting a suitable “title” and an appropriate “abstract” for an original research paper. Because the “title” and the “abstract” are the “initial impressions” or the “face” of a research article, they need to be drafted correctly, accurately, carefully, meticulously, and consume time and energy.[ 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 ] Often, these are drafted after the complete manuscript draft is ready.[ 2 , 3 , 4 , 5 , 9 , 10 , 11 ] Most readers will read only the title and the abstract of a published research paper, and very few “interested ones” (especially, if the paper is of use to them) will go on to read the full paper.[ 1 , 2 ] One must remember to adhere to the instructions laid down by the “target journal” (the journal for which the author is writing) regarding the style and number of words permitted for the title and the abstract.[ 2 , 4 , 5 , 7 , 8 , 9 , 12 ] Both the title and the abstract are the most important parts of a research paper – for editors (to decide whether to process the paper for further review), for reviewers (to get an initial impression of the paper), and for the readers (as these may be the only parts of the paper available freely and hence, read widely).[ 4 , 8 , 12 ] It may be worth for the novice author to browse through titles and abstracts of several prominent journals (and their target journal as well) to learn more about the wording and styles of the titles and abstracts, as well as the aims and scope of the particular journal.[ 5 , 7 , 9 , 13 ]
The details of the title are discussed under the subheadings of importance, types, drafting, and checklist.
When a reader browses through the table of contents of a journal issue (hard copy or on website), the title is the “ first detail” or “face” of the paper that is read.[ 2 , 3 , 4 , 5 , 6 , 13 ] Hence, it needs to be simple, direct, accurate, appropriate, specific, functional, interesting, attractive/appealing, concise/brief, precise/focused, unambiguous, memorable, captivating, informative (enough to encourage the reader to read further), unique, catchy, and it should not be misleading.[ 1 , 2 , 3 , 4 , 5 , 6 , 9 , 12 ] It should have “just enough details” to arouse the interest and curiosity of the reader so that the reader then goes ahead with studying the abstract and then (if still interested) the full paper.[ 1 , 2 , 4 , 13 ] Journal websites, electronic databases, and search engines use the words in the title and abstract (the “keywords”) to retrieve a particular paper during a search; hence, the importance of these words in accessing the paper by the readers has been emphasized.[ 3 , 4 , 5 , 6 , 12 , 14 ] Such important words (or keywords) should be arranged in appropriate order of importance as per the context of the paper and should be placed at the beginning of the title (rather than the later part of the title, as some search engines like Google may just display only the first six to seven words of the title).[ 3 , 5 , 12 ] Whimsical, amusing, or clever titles, though initially appealing, may be missed or misread by the busy reader and very short titles may miss the essential scientific words (the “keywords”) used by the indexing agencies to catch and categorize the paper.[ 1 , 3 , 4 , 9 ] Also, amusing or hilarious titles may be taken less seriously by the readers and may be cited less often.[ 4 , 15 ] An excessively long or complicated title may put off the readers.[ 3 , 9 ] It may be a good idea to draft the title after the main body of the text and the abstract are drafted.[ 2 , 3 , 4 , 5 ]
Titles can be descriptive, declarative, or interrogative. They can also be classified as nominal, compound, or full-sentence titles.
This has the essential elements of the research theme, that is, the patients/subjects, design, interventions, comparisons/control, and outcome, but does not reveal the main result or the conclusion.[ 3 , 4 , 12 , 16 ] Such a title allows the reader to interpret the findings of the research paper in an impartial manner and with an open mind.[ 3 ] These titles also give complete information about the contents of the article, have several keywords (thus increasing the visibility of the article in search engines), and have increased chances of being read and (then) being cited as well.[ 4 ] Hence, such descriptive titles giving a glimpse of the paper are generally preferred.[ 4 , 16 ]
This title states the main finding of the study in the title itself; it reduces the curiosity of the reader, may point toward a bias on the part of the author, and hence is best avoided.[ 3 , 4 , 12 , 16 ]
This is the one which has a query or the research question in the title.[ 3 , 4 , 16 ] Though a query in the title has the ability to sensationalize the topic, and has more downloads (but less citations), it can be distracting to the reader and is again best avoided for a research article (but can, at times, be used for a review article).[ 3 , 6 , 16 , 17 ]
From a sentence construct point of view, titles may be nominal (capturing only the main theme of the study), compound (with subtitles to provide additional relevant information such as context, design, location/country, temporal aspect, sample size, importance, and a provocative or a literary; for example, see the title of this review), or full-sentence titles (which are longer and indicate an added degree of certainty of the results).[ 4 , 6 , 9 , 16 ] Any of these constructs may be used depending on the type of article, the key message, and the author's preference or judgement.[ 4 ]
A stepwise process can be followed to draft the appropriate title. The author should describe the paper in about three sentences, avoiding the results and ensuring that these sentences contain important scientific words/keywords that describe the main contents and subject of the paper.[ 1 , 4 , 6 , 12 ] Then the author should join the sentences to form a single sentence, shorten the length (by removing redundant words or adjectives or phrases), and finally edit the title (thus drafted) to make it more accurate, concise (about 10–15 words), and precise.[ 1 , 3 , 4 , 5 , 9 ] Some journals require that the study design be included in the title, and this may be placed (using a colon) after the primary title.[ 2 , 3 , 4 , 14 ] The title should try to incorporate the Patients, Interventions, Comparisons and Outcome (PICO).[ 3 ] The place of the study may be included in the title (if absolutely necessary), that is, if the patient characteristics (such as study population, socioeconomic conditions, or cultural practices) are expected to vary as per the country (or the place of the study) and have a bearing on the possible outcomes.[ 3 , 6 ] Lengthy titles can be boring and appear unfocused, whereas very short titles may not be representative of the contents of the article; hence, optimum length is required to ensure that the title explains the main theme and content of the manuscript.[ 4 , 5 , 9 ] Abbreviations (except the standard or commonly interpreted ones such as HIV, AIDS, DNA, RNA, CDC, FDA, ECG, and EEG) or acronyms should be avoided in the title, as a reader not familiar with them may skip such an article and nonstandard abbreviations may create problems in indexing the article.[ 3 , 4 , 5 , 6 , 9 , 12 ] Also, too much of technical jargon or chemical formulas in the title may confuse the readers and the article may be skipped by them.[ 4 , 9 ] Numerical values of various parameters (stating study period or sample size) should also be avoided in the titles (unless deemed extremely essential).[ 4 ] It may be worthwhile to take an opinion from a impartial colleague before finalizing the title.[ 4 , 5 , 6 ] Thus, multiple factors (which are, at times, a bit conflicting or contrasting) need to be considered while formulating a title, and hence this should not be done in a hurry.[ 4 , 6 ] Many journals ask the authors to draft a “short title” or “running head” or “running title” for printing in the header or footer of the printed paper.[ 3 , 12 ] This is an abridged version of the main title of up to 40–50 characters, may have standard abbreviations, and helps the reader to navigate through the paper.[ 3 , 12 , 14 ]
Table 1 gives a checklist/useful tips for drafting a good title for a research paper.[ 1 , 2 , 3 , 4 , 5 , 6 , 12 ] Table 2 presents some of the titles used by the author of this article in his earlier research papers, and the appropriateness of the titles has been commented upon. As an individual exercise, the reader may try to improvise upon the titles (further) after reading the corresponding abstract and full paper.
Checklist/useful tips for drafting a good title for a research paper
The title needs to be simple and direct |
It should be interesting and informative |
It should be specific, accurate, and functional (with essential scientific “keywords” for indexing) |
It should be concise, precise, and should include the main theme of the paper |
It should not be misleading or misrepresentative |
It should not be too long or too short (or cryptic) |
It should avoid whimsical or amusing words |
It should avoid nonstandard abbreviations and unnecessary acronyms (or technical jargon) |
Title should be SPICED, that is, it should include Setting, Population, Intervention, Condition, End-point, and Design |
Place of the study and sample size should be mentioned only if it adds to the scientific value of the title |
Important terms/keywords should be placed in the beginning of the title |
Descriptive titles are preferred to declarative or interrogative titles |
Authors should adhere to the word count and other instructions as specified by the target journal |
Some titles used by author of this article in his earlier publications and remark/comment on their appropriateness
Title | Comment/remark on the contents of the title |
---|---|
Comparison of Pediatric Risk of Mortality III, Pediatric Index of Mortality 2, and Pediatric Index of Mortality 3 Scores in Predicting Mortality in a Pediatric Intensive Care Unit | Long title (28 words) capturing the main theme; site of study is mentioned |
A Prospective Antibacterial Utilization Study in Pediatric Intensive Care Unit of a Tertiary Referral Center | Optimum number of words capturing the main theme; site of study is mentioned |
Study of Ventilator-Associated Pneumonia in a Pediatric Intensive Care Unit | The words “study of” can be deleted |
Clinical Profile, Co-Morbidities & Health Related Quality of Life in Pediatric Patients with Allergic Rhinitis & Asthma | Optimum number of words; population and intervention mentioned |
Benzathine Penicillin Prophylaxis in Children with Rheumatic Fever (RF)/Rheumatic Heart Disease (RHD): A Study of Compliance | Subtitle used to convey the main focus of the paper. It may be preferable to use the important word “compliance” in the beginning of the title rather than at the end. Abbreviations RF and RHD can be deleted as corresponding full forms have already been mentioned in the title itself |
Performance of PRISM (Pediatric Risk of Mortality) Score and PIM (Pediatric Index of Mortality) Score in a Tertiary Care Pediatric ICU | Abbreviations used. “ICU” may be allowed as it is a commonly used abbreviation. Abbreviations PRISM and PIM can be deleted as corresponding full forms are already used in the title itself |
Awareness of Health Care Workers Regarding Prophylaxis for Prevention of Transmission of Blood-Borne Viral Infections in Occupational Exposures | Slightly long title (18 words); theme well-captured |
Isolated Infective Endocarditis of the Pulmonary Valve: An Autopsy Analysis of Nine Cases | Subtitle used to convey additional details like “autopsy” (i.e., postmortem analysis) and “nine” (i.e., number of cases) |
Atresia of the Common Pulmonary Vein - A Rare Congenital Anomaly | Subtitle used to convey importance of the paper/rarity of the condition |
Psychological Consequences in Pediatric Intensive Care Unit Survivors: The Neglected Outcome | Subtitle used to convey importance of the paper and to make the title more interesting |
Rheumatic Fever and Rheumatic Heart Disease: Clinical Profile of 550 patients in India | Number of cases (550) emphasized because it is a large series; country (India) is mentioned in the title - will the clinical profile of patients with rheumatic fever and rheumatic heart disease vary from country to country? May be yes, as the clinical features depend on the socioeconomic and cultural background |
Neurological Manifestations of HIV Infection | Short title; abbreviation “HIV” may be allowed as it is a commonly used abbreviation |
Krabbe Disease - Clinical Profile | Very short title (only four words) - may miss out on the essential keywords required for indexing |
Experience of Pediatric Tetanus Cases from Mumbai | City mentioned (Mumbai) in the title - one needs to think whether it is required in the title |
The details of the abstract are discussed under the subheadings of importance, types, drafting, and checklist.
The abstract is a summary or synopsis of the full research paper and also needs to have similar characteristics like the title. It needs to be simple, direct, specific, functional, clear, unbiased, honest, concise, precise, self-sufficient, complete, comprehensive, scholarly, balanced, and should not be misleading.[ 1 , 2 , 3 , 7 , 8 , 9 , 10 , 11 , 13 , 17 ] Writing an abstract is to extract and summarize (AB – absolutely, STR – straightforward, ACT – actual data presentation and interpretation).[ 17 ] The title and abstracts are the only sections of the research paper that are often freely available to the readers on the journal websites, search engines, and in many abstracting agencies/databases, whereas the full paper may attract a payment per view or a fee for downloading the pdf copy.[ 1 , 2 , 3 , 7 , 8 , 10 , 11 , 13 , 14 ] The abstract is an independent and stand-alone (that is, well understood without reading the full paper) section of the manuscript and is used by the editor to decide the fate of the article and to choose appropriate reviewers.[ 2 , 7 , 10 , 12 , 13 ] Even the reviewers are initially supplied only with the title and the abstract before they agree to review the full manuscript.[ 7 , 13 ] This is the second most commonly read part of the manuscript, and therefore it should reflect the contents of the main text of the paper accurately and thus act as a “real trailer” of the full article.[ 2 , 7 , 11 ] The readers will go through the full paper only if they find the abstract interesting and relevant to their practice; else they may skip the paper if the abstract is unimpressive.[ 7 , 8 , 9 , 10 , 13 ] The abstract needs to highlight the selling point of the manuscript and succeed in luring the reader to read the complete paper.[ 3 , 7 ] The title and the abstract should be constructed using keywords (key terms/important words) from all the sections of the main text.[ 12 ] Abstracts are also used for submitting research papers to a conference for consideration for presentation (as oral paper or poster).[ 9 , 13 , 17 ] Grammatical and typographic errors reflect poorly on the quality of the abstract, may indicate carelessness/casual attitude on part of the author, and hence should be avoided at all times.[ 9 ]
The abstracts can be structured or unstructured. They can also be classified as descriptive or informative abstracts.
Structured abstracts are followed by most journals, are more informative, and include specific subheadings/subsections under which the abstract needs to be composed.[ 1 , 7 , 8 , 9 , 10 , 11 , 13 , 17 , 18 ] These subheadings usually include context/background, objectives, design, setting, participants, interventions, main outcome measures, results, and conclusions.[ 1 ] Some journals stick to the standard IMRAD format for the structure of the abstracts, and the subheadings would include Introduction/Background, Methods, Results, And (instead of Discussion) the Conclusion/s.[ 1 , 2 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 17 , 18 ] Structured abstracts are more elaborate, informative, easy to read, recall, and peer-review, and hence are preferred; however, they consume more space and can have same limitations as an unstructured abstract.[ 7 , 9 , 18 ] The structured abstracts are (possibly) better understood by the reviewers and readers. Anyway, the choice of the type of the abstract and the subheadings of a structured abstract depend on the particular journal style and is not left to the author's wish.[ 7 , 10 , 12 ] Separate subheadings may be necessary for reporting meta-analysis, educational research, quality improvement work, review, or case study.[ 1 ] Clinical trial abstracts need to include the essential items mentioned in the CONSORT (Consolidated Standards Of Reporting Trials) guidelines.[ 7 , 9 , 14 , 19 ] Similar guidelines exist for various other types of studies, including observational studies and for studies of diagnostic accuracy.[ 20 , 21 ] A useful resource for the above guidelines is available at www.equator-network.org (Enhancing the QUAlity and Transparency Of health Research). Unstructured (or non-structured) abstracts are free-flowing, do not have predefined subheadings, and are commonly used for papers that (usually) do not describe original research.[ 1 , 7 , 9 , 10 ]
The four-point structured abstract: This has the following elements which need to be properly balanced with regard to the content/matter under each subheading:[ 9 ]
Background and/or Objectives: This states why the work was undertaken and is usually written in just a couple of sentences.[ 3 , 7 , 8 , 9 , 10 , 12 , 13 ] The hypothesis/study question and the major objectives are also stated under this subheading.[ 3 , 7 , 8 , 9 , 10 , 12 , 13 ]
Methods: This subsection is the longest, states what was done, and gives essential details of the study design, setting, participants, blinding, sample size, sampling method, intervention/s, duration and follow-up, research instruments, main outcome measures, parameters evaluated, and how the outcomes were assessed or analyzed.[ 3 , 7 , 8 , 9 , 10 , 12 , 13 , 14 , 17 ]
Results/Observations/Findings: This subheading states what was found, is longer, is difficult to draft, and needs to mention important details including the number of study participants, results of analysis (of primary and secondary objectives), and include actual data (numbers, mean, median, standard deviation, “P” values, 95% confidence intervals, effect sizes, relative risks, odds ratio, etc.).[ 3 , 7 , 8 , 9 , 10 , 12 , 13 , 14 , 17 ]
Conclusions: The take-home message (the “so what” of the paper) and other significant/important findings should be stated here, considering the interpretation of the research question/hypothesis and results put together (without overinterpreting the findings) and may also include the author's views on the implications of the study.[ 3 , 7 , 8 , 9 , 10 , 12 , 13 , 14 , 17 ]
The eight-point structured abstract: This has the following eight subheadings – Objectives, Study Design, Study Setting, Participants/Patients, Methods/Intervention, Outcome Measures, Results, and Conclusions.[ 3 , 9 , 18 ] The instructions to authors given by the particular journal state whether they use the four- or eight-point abstract or variants thereof.[ 3 , 14 ]
Descriptive abstracts are short (75–150 words), only portray what the paper contains without providing any more details; the reader has to read the full paper to know about its contents and are rarely used for original research papers.[ 7 , 10 ] These are used for case reports, reviews, opinions, and so on.[ 7 , 10 ] Informative abstracts (which may be structured or unstructured as described above) give a complete detailed summary of the article contents and truly reflect the actual research done.[ 7 , 10 ]
It is important to religiously stick to the instructions to authors (format, word limit, font size/style, and subheadings) provided by the journal for which the abstract and the paper are being written.[ 7 , 8 , 9 , 10 , 13 ] Most journals allow 200–300 words for formulating the abstract and it is wise to restrict oneself to this word limit.[ 1 , 2 , 3 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 22 ] Though some authors prefer to draft the abstract initially, followed by the main text of the paper, it is recommended to draft the abstract in the end to maintain accuracy and conformity with the main text of the paper (thus maintaining an easy linkage/alignment with title, on one hand, and the introduction section of the main text, on the other hand).[ 2 , 7 , 9 , 10 , 11 ] The authors should check the subheadings (of the structured abstract) permitted by the target journal, use phrases rather than sentences to draft the content of the abstract, and avoid passive voice.[ 1 , 7 , 9 , 12 ] Next, the authors need to get rid of redundant words and edit the abstract (extensively) to the correct word count permitted (every word in the abstract “counts”!).[ 7 , 8 , 9 , 10 , 13 ] It is important to ensure that the key message, focus, and novelty of the paper are not compromised; the rationale of the study and the basis of the conclusions are clear; and that the abstract is consistent with the main text of the paper.[ 1 , 2 , 3 , 7 , 9 , 11 , 12 , 13 , 14 , 17 , 22 ] This is especially important while submitting a revision of the paper (modified after addressing the reviewer's comments), as the changes made in the main (revised) text of the paper need to be reflected in the (revised) abstract as well.[ 2 , 10 , 12 , 14 , 22 ] Abbreviations should be avoided in an abstract, unless they are conventionally accepted or standard; references, tables, or figures should not be cited in the abstract.[ 7 , 9 , 10 , 11 , 13 ] It may be worthwhile not to rush with the abstract and to get an opinion by an impartial colleague on the content of the abstract; and if possible, the full paper (an “informal” peer-review).[ 1 , 7 , 8 , 9 , 11 , 17 ] Appropriate “Keywords” (three to ten words or phrases) should follow the abstract and should be preferably chosen from the Medical Subject Headings (MeSH) list of the U.S. National Library of Medicine ( https://meshb.nlm.nih.gov/search ) and are used for indexing purposes.[ 2 , 3 , 11 , 12 ] These keywords need to be different from the words in the main title (the title words are automatically used for indexing the article) and can be variants of the terms/phrases used in the title, or words from the abstract and the main text.[ 3 , 12 ] The ICMJE (International Committee of Medical Journal Editors; http://www.icmje.org/ ) also recommends publishing the clinical trial registration number at the end of the abstract.[ 7 , 14 ]
Table 3 gives a checklist/useful tips for formulating a good abstract for a research paper.[ 1 , 2 , 3 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 14 , 17 , 22 ]
Checklist/useful tips for formulating a good abstract for a research paper
The abstract should have simple language and phrases (rather than sentences) |
It should be informative, cohesive, and adhering to the structure (subheadings) provided by the target journal. Structured abstracts are preferred over unstructured abstracts |
It should be independent and stand-alone/complete |
It should be concise, interesting, unbiased, honest, balanced, and precise |
It should not be misleading or misrepresentative; it should be consistent with the main text of the paper (especially after a revision is made) |
It should utilize the full word capacity allowed by the journal so that most of the actual scientific facts of the main paper are represented in the abstract |
It should include the key message prominently |
It should adhere to the style and the word count specified by the target journal (usually about 250 words) |
It should avoid nonstandard abbreviations and (if possible) avoid a passive voice |
Authors should list appropriate “keywords” below the abstract (keywords are used for indexing purpose) |
This review article has given a detailed account of the importance and types of titles and abstracts. It has also attempted to give useful hints for drafting an appropriate title and a complete abstract for a research paper. It is hoped that this review will help the authors in their career in medical writing.
Conflicts of interest.
There are no conflicts of interest.
The author thanks Dr. Hemant Deshmukh - Dean, Seth G.S. Medical College & KEM Hospital, for granting permission to publish this manuscript.
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I regularly assign my undergraduate students papers with a range of expected page/word length (e.g. 10-12 pages or 2500-3000 words). Is there any sort of rule as to whether or not to count a works cited page(s0 (and its equivalent in the other citation styles) in determining if a paper meets this limit? I've discussed this with colleagues and heard varying answers.
In the scientific world, whether citations count against length limits or not varies wildly by publication, including hybrid models like AAAI which allows six pages text and up to one page of citations.
I think that which way you go depends on what you want the students to learn. Some examples that would push you one way or another:
If you want them to focus on prose, don't count citations in the length.
If you want them to learn to express complicated thoughts concisely, use a short page limit and count citations (e.g., the IEEE six-page format)
If you want them to focus on referencing, count citations and text separately.
Either way it shouldn't matter too much, because you're using a range and probably have some flexibility in how you apply your rubric, so you can adjust for common sense.
Should not count.
A six-line main text can pack more convincing arguments compared to a one-line main text. That's why it's important to make sure all students have an equal share of area or real property to build upon.
A six-line citation does not necessarily bring any advantage compared to a one-line citation. For that reason, I don't see why we should penalize students who had identified some information with more authors or a longer title; that is not how we teach them to examine the credibility of a paper.
If you're concerned about them citing too many things or citing mindlessly, you may put a limit on the number of citations like some journals do. However, I wouldn't include them in the word count.
IMAGES
COMMENTS
1- The median length of a research paper is 4,133 words (equivalent to 166 sentences or 34 paragraphs), excluding the abstract and references, with 90% of papers being between 2,023 and 8,284 words. 2- A typical article is divided in the following way: Introduction section: 14.6% of the total word count. Methods section: 29.7% of the total word ...
It provides an overview of the paper and helps readers decide whether to read the full text. Limit your abstract to 250 words. 1. Abstract Content . The abstract addresses the following (usually 1-2 sentences per topic): • key aspects of the literature review • problem under investigation or research question(s) • clearly stated ...
Manuscripts can include an unlimited number of figures, tables and additional files but the abstract of the manuscript should not exceed 350 words. However, please remember that for the benefit of peer reviewers and readers articles should be as concise as possible. For any additional questions, please contact the relevant submission contact of ...
Abstract: Limit to 175 words References: Limit to 50 Tables & Figures: Limit to 4 Research articles should present original research that describes outcomes, processes, or applications that enhance the patient experience. A range of methods, including qualitative research, quantitative research, and experimental studies are accepted.
The abstract may also be the only part of your paper that has a word limit. Most word limits specify a maximum of between 250 and 300 words, and some journals require that abstracts be as short as 150 words. Writing a great abstract is almost an art—but writing an abstract that meets word limits is, well, a science.
However, to enable typesetting of papers, we advise making the number of display items commensurate with your overall word length. So, for Articles of 2,000 words or less, we suggest including no ...
An APA abstract is a 150-250 word summary of your paper. Learn how to write and format it with an easy example! (APA 6th & 7th edition) ... Limit the length to 250 words. ... To help potential readers determine the relevance of your paper for their own research.
There are two main reasons that academic papers usually come with a word limit: Fairness. It's impossible to grade two papers of vastly different lengths (e.g., 20,000 compared to 2,000 words) on the same scale. The word limit makes sure that everyone taking the same class knows what is expected of them. Communication Skills.
Answer: Front matter such as title, author, and abstract and end matter such as references and acknowledgments are typically not included in the manuscript word count. The main text and also tables, figures, and captions for them are included in the count. The title has its own word limit (say about 10-15 max), so too the abstract (about 200 ...
For research papers (Original Articles), IntJUrolallows authors a maximum of 3000 words including abstracts, but excluding references, tables and figures. Other medical journals have other restrictions, but often ask you for 3000-4000 words.You may find it helpful to write a preliminary abstract as a structural guide for the larger manuscript.1
The word count limit for an entire paper will be set by the journal to which you are submitting your work or by your professor for a university assignment. Limits vary widely and are dependent on the nature of the article you are writing—for example, a brief report will be short but a dissertation quite long.
it depends upon the journal and type of articles and it differs from journal to journal . original article it ranges from 2,500 -3000 word s limit witout abstract and references. Cite. 4 ...
Here's a summary of the key findings. 1. The median title was 14 words long (equivalent to 103 characters), and 90% of titles in the sample were between 6 and 25 words. 2. The 10-year trend shows an increase in title length from an average of 103 characters in 2012 to 111 characters in 2021. 3.
Coming to your manuscript though, as the number of pages for your tables/graphs is quite a bit, you may need to look more at the page count. So, 6500 words is fine, and so is 15 text pages. But the number of reference pages (4) and figures/tables pages (8) is where you are having the issue. These are taking the count up to 27, which is way more ...
Articles must have a clear methodological focus, and not simply present findings from qualitative studies. They should be between 7,500 and 8,500 words, excluding references. Any articles that fall below or above that range will be returned. Notes is a new format for short, engaging and imaginative submissions.
Word counts exist for many reasons—print publications, for example, have them to ensure stories can fit in a defined space in a newspaper, magazine, or book. But when it comes to research papers and essays, word counts are used to level the playing field: Each student has the same number of words to get their point across. A strong writer can ...
TIP: Journals often set a maximum word count for Abstracts, often 250 words, and no citations. This is to ensure that the full Abstract appears in indexing services. Keywords are a tool to help indexers and search engines find relevant papers. If database search engines can find your journal manuscript, readers will be able to find it too.
12-25 words. Generically speaking, there are no known definite rules on words limit for research topics conventionally. However, research topics must not be ambiguous, meaningless, verbose or ...
To encourage full and transparent reporting of research we do not set fixed word count limits for research articles. Nonetheless, we ask you to make your article concise and make every word count. ... We require a data sharing statement for all research papers. For papers that do not report a trial, we do not require that the authors agree to ...
When you have little time to spare, small changes to your text can add up to the space you need. Here are a few simple tricks you can use to quickly tighten your text and meet the limit. 1. Delete "The". You can often omit the word "the" from your text without losing any meaning.
The title and abstracts are the only sections of the research paper that are often freely available to the readers on the journal websites, ... Most journals allow 200-300 words for formulating the abstract and it is wise to restrict oneself to this word limit.[1,2,3,7,8,9,10,11,12,13,22] Though some authors prefer to draft the abstract ...
Our papers always had a word limit. Taking a topic about which you could write 50 pages and distilling it down to the 5 pages to which you are limited is a great way to tone up your thoughts and produce a much better argument. Once you get out of academia, brevity is valued - summarizing something in a page is what is expected of you. ...
I regularly assign my undergraduate students papers with a range of expected page/word length (e.g. 10-12 pages or 2500-3000 words). Is there any sort of rule as to whether or not to count a works cited page(s0 (and its equivalent in the other citation styles) in determining if a paper meets this limit?