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InsightsJournal and publisher policy

Policy briefBMJ journals

The BMJ Requires a Patient and Public Involvement Statement in the Methods

BMJ requires every research paper to carry a Patient and Public Involvement statement, and it has to sit in the methods section, at submission. The statement describes how patients and the public were involved in the research. Saying that they were not involved is a complete answer; leaving the statement out is not. CONSORT 2025 added the same requirement to the trial reporting checklist (BMJ, n.d.).

Pubrica InsightsWritten by the publication and regulatory teams Published8 October 2026 Last checked8 October 2026 Reading time7 minutes Sources2
  • Required in all research papers
  • Inside the methods section
  • At submission
  • “Not involved” is a valid answer
  • Now a CONSORT item too

In force BMJ journals

Instrument
Patient and public partnership
Issued by
BMJ Publishing Group
Date on the page
None shown. Page metadata records a modification date of 4 August 2026.
Applies to
Research papers submitted to BMJ journals
What you must do
Include a Patient and Public Involvement statement within the methods section at submission, describing how patients and the public were involved in the research.
Patient co-authors
A patient author “must meet the same ICMJE criteria as a standard author”, and may be required to give consent for publication where the article includes their own health information.
Primary source
Patient and public partnership
BMJ Author Hub · read 8 October 2026

Read the policy itself

What this policy is, in plain words.

The requirement is short and the placement is the part people get wrong. “All authors submitting research papers are required to include a” Patient and Public Involvement Statement “within the methods section of their paper at submission.”

Three things follow from that wording. It applies to research papers, not to every article type. It goes in the methods, not in a cover letter or a declarations block at the end. And it is due at submission, not on request during review.

What the statement has to say is how patients and the public were involved in the research — in setting the question, designing the study, choosing the outcomes, conducting it, or disseminating the results. BMJ also notes that it is revising how it asks the question in order to standardise the responses.

Patient co-authors. Where a patient is named as an author, they “must meet the same ICMJE criteria as a standard author”, and they may be required to provide consent for publication where the article includes information about their own health or conditions. Involvement and authorship are different thresholds, and conflating them does the patient no favours.

Why it exists.

The statement exists because research funded to help patients has a long history of measuring things patients do not care about. A trial that chose its primary outcome without asking anybody who has the condition can be methodologically immaculate and clinically beside the point.

Requiring the statement rather than the practice is deliberate and worth understanding. BMJ is not insisting that every study involve patients; it is insisting that the reader be told. A paper that states plainly that there was no patient or public involvement has complied, and has also told a funder and a reader something true about how the question was chosen.

CONSORT 2025 added patient and public involvement as item 8 of its checklist in April 2025, which means a randomised trial now meets the same requirement twice — once from the journal and once from the reporting guideline. For trialists that convergence is the practical news.

What you have to do.

Five things about a statement that takes three sentences

Put the statement in the methods, under its own subheadingNot in the cover letter, not in the declarations at the end
Write it before submissionThe requirement attaches at submission, not at revision
If there was no involvement, say so plainlyThat is a complete answer; an absent statement is not
Describe the stage, not the sentimentQuestion setting, design, outcome choice, conduct, dissemination
If a patient is a co-author, check they meet the ICMJE criteriaAnd whether they need to consent to their own health information appearing

It is the cheapest item on any reporting checklist and one of the most commonly missing. Three honest sentences in the methods, written before submission, remove an entire category of revision request.

Who and what it reaches.

What it reaches — by subject, by the people it falls on, and by territory.

Subjects

Research papers in BMJ journals

All research paper submissions, across the specialties BMJ publishes. Not editorials, not correspondence.

Population

Patients and the public as contributors, not subjects

The statement is about people involved in shaping the research, which is a different group from the participants enrolled in it.

Countries

No territorial limit

Applies to BMJ journals wherever the authors are. National funders in the UK and elsewhere have parallel involvement expectations.

Which journals apply it, and how.

How it reaches a specific journal. The policy is publisher-level across BMJ’s research journals. The page names no individual titles, stating simply that all authors submitting research papers are required to include the statement.

Beyond BMJ. Since CONSORT 2025 made patient and public involvement item 8 of the trial checklist, any journal that asks for a completed CONSORT checklist is now asking the same question of a randomised trial, whoever publishes it.

The questions people actually ask.

Not by itself. The requirement is for a statement, not for a practice. What a reviewer may ask is whether involvement would have changed the outcome selection — which is a question about the study, not about the statement.

Describe it accurately and let the reader judge. Say what the group was asked, at what stage, and what changed as a result. “We consulted a patient advisory group” with nothing after it is the version that draws a follow-up question.

Yes, if they meet the ICMJE criteria in the same way as any other author — all four, including accountability for the work. BMJ may also ask them to consent to publication where their own health information appears in the paper.

Under its own subheading, at the end of the methods section, is the convention and the easiest for an editor to find. The policy requires it within the methods and does not fix the position inside it.

The policy page itself gives no date. BMJ-published research describing the policy puts its introduction in 2014, but that is a study describing the policy rather than the policy page stating its own date, and we would rather tell you that than present it as though the page said so.

Sources

Every claim above rests on one of these. Each was read on the date shown; a policy can move after that.

  1. 1BMJ Publishing Group. (n.d.). Patient and public partnership. BMJ Author Hub. No date is shown on the page; its metadata records a modification date of 4 August 2026.
    https://authors.bmj.com/policies/patient-public-partnership/ Read 8 October 2026.
  2. 2Hopewell, S., et al. (2025, April 14). CONSORT 2025 statement. PLOS Medicine, 22(4), e1004587. Patient and public involvement is new item 8 of the checklist.
    https://pmc.ncbi.nlm.nih.gov/articles/PMC11996237 Read 8 October 2026.

BMJpatient and public involvementPPICONSORTmethodsphysicians

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Pubrica Insights. (2026, October 8). The BMJ Requires a Patient and Public Involvement Statement in the Methods. Pubrica. https://pubrica.com/insights/bmj-patient-public-involvement-statement/

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