GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research
Open accessAbstract
While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why. To develop international consensus on the key items to report to enhance the quality, transparency, and consistency of the PPI evidence base. To collaboratively involve patients as research partners at all stages in the development of GRIPP2. The EQUATOR method for developing reporting guidelines was used. The original GRIPP (Guidance for Reporting Involvement of Patients and the Public) checklist was revised, based on updated systematic review evidence. A three round Delphi survey was used to develop consensus on items to be included in the guideline. A subsequent face-to-face meeting produced agreement on items not reaching consensus during the Delphi process. One hundred forty-three participants agreed to participate in round one, with an 86% (123/143) response for round two and a 78% (112/143) response for round three. The Delphi survey identified the need for long form (LF) and short form (SF) versions. GRIPP2-LF includes 34 items on aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections and is suitable for studies where the main focus is PPI. GRIPP2-SF includes five items on aims, methods, results, outcomes, and critical perspective and is suitable for studies where PPI is a secondary focus. GRIPP2-LF and GRIPP2-SF represent the first international evidence based, consensus informed guidance for reporting patient and public involvement in research. Both versions of GRIPP2 aim to improve the quality, transparency, and consistency of the international PPI evidence base, to ensure PPI practice is based on the best evidence. In order to encourage its wide dissemination this article is freely accessible on The BMJ and Research Involvement and Engagement journal websites.
AI snapshot
Written from the paper’s full text.
TL;DR
GRIPP2-LF and GRIPP2-SF are consensus-based reporting checklists for patient and public involvement (PPI) in research, developed using EQUATOR methods, a three-round Delphi survey, and a consensus meeting. GRIPP2-LF has 34 items for studies where PPI is the primary focus; GRIPP2-SF has five items for studies where PPI is a secondary focus.
Key findings
- The Delphi survey included 143 participants in round one, with an 86% (123/143) response in round two and 78% (112/143) in round three. The five core GRIPP2-SF items each gained a median score of 9 in round two and again in round three.
- GRIPP2-LF includes 34 items covering aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections.
- GRIPP2-SF includes five items: aims, methods, results, outcomes, and critical perspective.
- The final consensus meeting involved 25 key experts, including patient partners and carers (n = 8), researchers (n = 9), clinicians (n = 6), and healthcare journal editors (n = 2), and finalised consensus on seven items on the threshold of consensus.
Methods
- The study used the EQUATOR method for developing reporting guidelines: updated systematic review evidence, a three-round Delphi survey with international PPI stakeholders, and a face-to-face consensus meeting.
- Delphi participants rated items on a 1–10 scale; median ≥8 in rounds one and two indicated positive consensus, median ≤5 excluded items, and items scoring 6 or 7 in one round and ≥8 in the other were voted on again in round three, with positive consensus if median ≥8 in two rounds.
- Three patient partners were recruited to the research team and were involved in refining research questions, developing the search strategy, interpreting results, selecting original GRIPP items, piloting the Delphi survey, recruiting participants, collating comments, adapting items, and writing up the study.
Limitations
- The paper states that usability testing has not yet been possible to understand how GRIPP2 works in practice with different study designs, and that the final consensus meeting did not include international experts because of a restricted budget, which might have limited the discussion from an international perspective.
- The paper states that GRIPP2 is conceptualised within the culture and language of research, that a patient or service-user version is needed but not yet developed, and that it is not possible to be prescriptive about the exact content of each item because the current evidence base is not advanced enough.
- The paper also states that the EQUATOR consensus methods limited possible patient partner input into identifying or developing methods to gain consensus, that feedback time between Delphi rounds was short, and that scheduling meetings between researchers and patient partners was difficult; further refinements are expected as the PPI evidence base evolves.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 23 cited sources checked · 0 supported · 0 flagged
- Findingown data
The Delphi survey identified the need for long form (LF) and short form (SF) versions of the guideline.
“The Delphi survey identified the need for long form (LF) and short form (SF) versions.”
Quote in the paperSubstantial claim - Premisecitation
The original GRIPP checklist's development drew on systematic review evidence, without broader input from the international PPI research community.
“While the original GRIPP checklist represented an important starting point in creating high quality PPI reporting, its development drew on systematic review evidence, without broader input from the international PPI research community [2–4].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [2] Brett J, Staniszewska S, Mockford C, et al. Mapping the impact of patient and public involvement on health and social care research: a systematic review. Health Expect. 2014;17:637–50. doi: 10.1111/j.1369-7625.2012.00795.x . source
Not checked in the free run.
- cites [3] Mockford C, Staniszewska S, Griffiths F, Herron-Marx S. The impact of patient and public involvement on UK NHS health care: a systematic review. Int J Qual Health Care. 2012;24:28–38. doi: 10.1093/intqhc/mzr066 . source
Not checked in the free run.
- cites [4] Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7:387–95. doi: 10.1007/s40271-014-0065-0 . source
Not checked in the free run.
- Interpretationreasoning
Inconsistent reporting creates a fragmented evidence base making it difficult to draw together understanding of what works, for whom, why, and in what context.
“Inconsistent reporting creates a fragmented evidence base making it difficult to draw together our collective understanding of what works, for whom, why, and in what context.”
Quote in the paperSubstantial claim - Premisecitation
The original GRIPP checklist tackled inconsistent reporting by helping researchers, patients, carers, and the public to improve the quality, consistency, and transparency of PPI reporting.
“This prompted the development of the original Guidance for Reporting Involvement of Patients and the Public (GRIPP), which tackled inconsistent reporting by helping researchers, patients, carers, and the public to improve the quality, consistency, and transparency of PPI reporting, to strengthen the quality of the international PPI evidence base [1].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] Staniszewska S, Brett J, Mockford C, Barber R. The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research. Int J Technol Assess Health Care. 2011;27:391–9. doi: 10.1017/S0266462311000481 . source
Not checked in the free run.
- Premisecitation
Inadequate reporting of PPI creates problems for systematic reviews that attempt to synthesise PPI evidence.
“Inadequate reporting can create problems for systematic reviews that attempt to synthesise PPI evidence [2–4].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [2] Brett J, Staniszewska S, Mockford C, et al. Mapping the impact of patient and public involvement on health and social care research: a systematic review. Health Expect. 2014;17:637–50. doi: 10.1111/j.1369-7625.2012.00795.x . source
Not checked in the free run.
- cites [3] Mockford C, Staniszewska S, Griffiths F, Herron-Marx S. The impact of patient and public involvement on UK NHS health care: a systematic review. Int J Qual Health Care. 2012;24:28–38. doi: 10.1093/intqhc/mzr066 . source
Not checked in the free run.
- cites [4] Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7:387–95. doi: 10.1007/s40271-014-0065-0 . source
Not checked in the free run.
- Study design and conductown data
The original GRIPP checklist was revised based on updated systematic review evidence.
“The original GRIPP (Guidance for Reporting Involvement of Patients and the Public) checklist was revised, based on updated systematic review evidence.”
Quote in the paperSubstantial claim - Premisecitation
PPI in research can improve the relevance and overall quality of research by ensuring it focuses on issues of importance to patients.
“PPI in research can improve the relevance and overall quality of research, by ensuring that it focuses on the issues of importance to patients [1].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] Staniszewska S, Brett J, Mockford C, Barber R. The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research. Int J Technol Assess Health Care. 2011;27:391–9. doi: 10.1017/S0266462311000481 . source
Not checked in the free run.
- Study design and conductcitation
The study used the EQUATOR method for developing reporting guidelines.
“The study used the EQUATOR method for developing reporting guidelines [5], which included: systematic review evidence; a three stage Delphi survey including key stakeholders in the field of PPI; and a face-to-face collaborative meeting to develop consensus on items outstanding from the Delphi survey.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [5] Moher D, Schulz KF, Simera I, Altman DG. Guidance for developers of health research reporting guidelines. PLoS Med. 2010;7:e1000217. doi: 10.1371/journal.pmed.1000217 . source
Not checked in the free run.
- Interpretationnone given
GRIPP2-LF and GRIPP2-SF represent the first international evidence based, consensus informed guidance for reporting patient and public involvement in research.
“GRIPP2-LF and GRIPP2-SF represent the first international evidence based, consensus informed guidance for reporting patient and public involvement in research.”
Quote in the paperSubstantial claim - Interpretationcitation
It is not possible to be prescriptive about the exact content of each GRIPP2 item because the current evidence base is not advanced enough.
“While GRIPP2-LF and GRIPP2-SF aim to guide consistent reporting, it is not possible to be prescriptive about the exact content of each item, as the current evidence base is not advanced enough to make this possible [2–4, 21].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [2] Brett J, Staniszewska S, Mockford C, et al. Mapping the impact of patient and public involvement on health and social care research: a systematic review. Health Expect. 2014;17:637–50. doi: 10.1111/j.1369-7625.2012.00795.x . source
Not checked in the free run.
- cites [3] Mockford C, Staniszewska S, Griffiths F, Herron-Marx S. The impact of patient and public involvement on UK NHS health care: a systematic review. Int J Qual Health Care. 2012;24:28–38. doi: 10.1093/intqhc/mzr066 . source
Not checked in the free run.
- cites [4] Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7:387–95. doi: 10.1007/s40271-014-0065-0 . source
Not checked in the free run.
- cites [21] Wilson P, Mathie E, Keenan J, et al. ReseArch with Patient and Public involvement: a RealisT evaluation—the RAPPORT study: Health Services and Delivery Research; 2015. p. 3. doi: 10.3310/hsdr03380 . source
Not checked in the free run.
- Classified as probably not a substantial claim. 17
- May combine two claims. 7
Classified as probably not a substantial claim.
Findingown dataGRIPP2-LF includes 34 items on aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections.
“GRIPP2-LF includes 34 items on aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections and is suitable for studies where the main focus is PPI.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Findingown dataOne hundred forty-three participants agreed to participate in round one, with an 86% (123/143) response for round two and a 78% (112/143) response for round three.
“One hundred forty-three participants agreed to participate in round one, with an 86% (123/143) response for round two and a 78% (112/143) response for round three.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataThe consensus meeting involved eight patient partners in total.
“The consensus meeting involved eight patient partners in total, and the three patient partners recruited to the research team were involved in the write-up of the study and are coauthors in papers.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Findingown dataGRIPP2-SF includes five items on aims, methods, results, outcomes, and critical perspective.
“GRIPP2-SF includes five items on aims, methods, results, outcomes, and critical perspective and is suitable for studies where PPI is a secondary focus.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataQualitative comments suggested the need to reword some items to simplify them and ensure clarity of meaning.
“Qualitative comments suggested the need to reword some items to simplify them and ensure clarity of meaning.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataThe five core items that comprise GRIPP2-SF all gained a median score of 9 in round two and again in round three, indicating consensus was reached on the short form version.
“The five core items that comprise the GRIPP2-SF all gained a median score of 9 in round two. Thus all five were included in round three and again gained median scores of 9, indicating that consensus was reached on the short form version.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationThe quality of reporting of patient and public involvement in research papers is often inconsistent and partial, with little information about context, process, and impact.
“While the patient and public involvement (PPI) evidence base has expanded over the past decade, the quality of reporting within papers is often inconsistent, limiting our understanding of how it works, in what context, for whom, and why.”
- Also stated in: § Background · plain
“While the PPI evidence base has expanded significantly over the past decade, the reporting of PPI in papers has often been inconsistent and partial, with little information about the context, process, and impact of public involvement and with limited reporting of conceptualisation or theorisation [1–4].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [1] Staniszewska S, Brett J, Mockford C, Barber R. The GRIPP checklist: strengthening the quality of patient and public involvement reporting in research. Int J Technol Assess Health Care. 2011;27:391–9. doi: 10.1017/S0266462311000481 . source
Not checked in the free run.
- cites [2] Brett J, Staniszewska S, Mockford C, et al. Mapping the impact of patient and public involvement on health and social care research: a systematic review. Health Expect. 2014;17:637–50. doi: 10.1111/j.1369-7625.2012.00795.x . source
Not checked in the free run.
- cites [3] Mockford C, Staniszewska S, Griffiths F, Herron-Marx S. The impact of patient and public involvement on UK NHS health care: a systematic review. Int J Qual Health Care. 2012;24:28–38. doi: 10.1093/intqhc/mzr066 . source
Not checked in the free run.
- cites [4] Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7:387–95. doi: 10.1007/s40271-014-0065-0 . source
Not checked in the free run.
- Also stated in: § Background · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenA subsequent face-to-face meeting produced agreement on items not reaching consensus during the Delphi process.
“A subsequent face-to-face meeting produced agreement on items not reaching consensus during the Delphi process.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
PremisecitationAchieving consensus is acknowledged as a crucial step in producing a reporting guideline.
“Achieving consensus is now acknowledged as a crucial step in producing a reporting guideline [5].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [5] Moher D, Schulz KF, Simera I, Altman DG. Guidance for developers of health research reporting guidelines. PLoS Med. 2010;7:e1000217. doi: 10.1371/journal.pmed.1000217 . source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataA three round Delphi survey was used to develop consensus on items to be included in the guideline.
“A three round Delphi survey was used to develop consensus on items to be included in the guideline.”
Quote in the paperNot a substantial claimMay combine two claims.
Study design and conductnone givenThe final consensus meeting did not include international experts because of a restricted budget, which might have limited the discussion from an international perspective.
“The final consensus meeting did not include international experts because of a restricted budget, which might have limited the discussion from an international perspective.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenNo usability testing has yet been conducted to understand how GRIPP2 works in practice with different types of study designs.
“In addition, it has not yet been possible to conduct any usability testing to understand how GRIPP2 works in practice with different types of study designs.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
InterpretationreasoningGRIPP2-SF is suitable for studies where PPI is a secondary focus.
“GRIPP2-SF includes five items on aims, methods, results, outcomes, and critical perspective and is suitable for studies where PPI is a secondary focus.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationThe success of PPI in this study may relate to several factors, including patient partners' prior training, researchers' experience, and good relationships.
“The success of the PPI in this study may relate to several factors. Firstly, the patient partners had received training around research methods in previous studies and were actively involved in a patient and public involvement group attached to the University of Warwick Medical School. Furthermore, the researchers were experienced at involving patient partners in their research [22]. Finally, good”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [22] Stephens R, Staniszewska S. One small step…. Research Involvement and Engagement; 2015. p. 1. doi: 10.1186/s40900-015-0005-8 . source
Not checked in the free run.
- cites [4] Brett J, Staniszewska S, Mockford C, et al. A systematic review of the impact of patient and public involvement on service users, researchers and communities. Patient. 2014;7:387–95. doi: 10.1007/s40271-014-0065-0 . source
Not checked in the free run.
- cites [21] Wilson P, Mathie E, Keenan J, et al. ReseArch with Patient and Public involvement: a RealisT evaluation—the RAPPORT study: Health Services and Delivery Research; 2015. p. 3. doi: 10.3310/hsdr03380 . source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based). May combine two claims.
InterpretationreasoningHigher quality reporting will gradually lead to the development of a stronger PPI evidence base that will facilitate more effective synthesis of PPI studies.
“Higher quality reporting will gradually lead to the development of a stronger PPI evidence base that will facilitate more effective synthesis of PPI studies.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
InterpretationreasoningGRIPP2-LF is suitable for studies where the main focus is PPI.
“GRIPP2-LF includes 34 items on aims, definitions, concepts and theory, methods, stages and nature of involvement, context, capture or measurement of impact, outcomes, economic assessment, and reflections and is suitable for studies where the main focus is PPI.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable), S4 (based). May combine two claims.
InterpretationreasoningMore effective synthesis of the PPI evidence base will help to identify best practice, avoid poor practice, and contribute to research that is acceptable, relevant, appropriate, and high quality.
“More effective synthesis of the PPI evidence base will help to identify best practice, avoid poor practice, and contribute to research that is acceptable, relevant, appropriate, and high quality and that has the potential to generate benefit for all.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
PremisecitationPPI is at a pre-paradigm stage in its development and recognition.
“Such evolution is particularly important for GRIPP2 because PPI is at a pre-paradigm stage in its development and recognition, reflecting Kuhn’s conceptualisation of how science changes over time with significant paradigm shifts that generate new ways of thinking [20].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] Kuhn TS. The structure of scientific Revolutions. 50th anniversary. Ian Hacking (Introd.). 4th ed: University of Chicago Press; 2012. p. 264. doi: 10.7208/chicago/9780226458144.001.0001 . source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenGRIPP2-LF and GRIPP2-SF are conceptualised within the culture and language of research.
“A further limitation is that GRIPP2-LF and GRIPP2-SF are conceptualised within the culture and language of research.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationGuidelines such as the CONSORT statement for randomised controlled trials are regularly updated to reflect changes in health research more widely.
“Guidelines such as the CONSORT statement for randomised controlled trials (RCTs) are regularly updated to reflect changes in health research more widely [19].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [19] Moher D, Hopewell S, Schulz KF, et al. CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials. BMJ. 2010;340:c869. doi: 10.1136/bmj.c869 . source
Not checked in the free run.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The PPIE strategy is presented in accordance with the GRIPP2 (short form) reporting guidelines.
“Our PPIE strategy is presented in accordance with the GRIPP2 (short form) reporting guidelines [35].”
From Layering perspectives: a structured approach to meaningful patient and public involvement and engagement in the RETURN dental trial (2026) · cites this paper as [35]
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Collins, G. S., Moons, K. G. M., Dhiman, P., Riley, R. D., Beam, A. L., Van Calster, B., Ghassemi, M., Liu, X., Reitsma, J. B., van Smeden, M., et al. (2024) · BMJ · doi:10.1136/bmj-2023-078378 · Cited by 4,718 · see citing works
Research co-design in health: a rapid overview of reviews
Slattery, P., Saeri, A. K., & Bragge, P. (2020) · Health Research Policy and Systems · doi:10.1186/s12961-020-0528-9 · Cited by 1,313 · see citing works
Greenhalgh, T., Hinton, L., Finlay, T., Macfarlane, A., Fahy, N., Clyde, B., & Chant, A. (2019) · Health Expectations · doi:10.1111/hex.12888 · Cited by 1,059 · see citing works
Calvert, M., Kyte, D., Mercieca-Bebber, R., Slade, A., Chan, A.-W., King, M. T., and the SPIRIT-PRO Group, Hunn, A., Bottomley, A., Regnault, A., et al. (2018) · JAMA · doi:10.1001/jama.2017.21903 · Cited by 814 · see citing works
Self-citationHusereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · Value in Health · doi:10.1016/j.jval.2021.10.008 · Cited by 847 · see citing works
Self-citationGattrell, W. T., Logullo, P., van Zuuren, E. J., Price, A., Hughes, E. L., Blazey, P., Winchester, C. C., Tovey, D., Goldman, K., Hungin, A. P., et al. (2024) · PLOS Medicine · doi:10.1371/journal.pmed.1004326 · Cited by 701 · see citing works
Skivington, K., Matthews, L., Simpson, S. A., Craig, P., Baird, J., Blazeby, J. M., Boyd, K., Craig, N. J., French, D., McIntosh, E., et al. (2021) · Health Technology Assessment · doi:10.3310/hta25570 · Cited by 535 · see citing works
Husereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E. W., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · BMJ · doi:10.1136/bmj-2021-067975 · Cited by 488 · see citing works
Self-citationDuncan, E., O'Cathain, A., Rousseau, N., Croot, L., Sworn, K., Turner, K. M., Yardley, L., & Hoddinott, P. (2020) · BMJ Open · doi:10.1136/bmjopen-2019-033516 · Cited by 481 · see citing works
How to engage stakeholders in research: design principles to support improvement
Boaz, A., Hanney, S. R., Borst, R. A. J., O’Shea, A., & Kok, M. O. (2018) · Health Research Policy and Systems · doi:10.1186/s12961-018-0337-6 · Cited by 471 · see citing works
Husereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · BMC Medicine · doi:10.1186/s12916-021-02204-0 · Cited by 450 · see citing works
Self-citationDecision aids for people facing health treatment or screening decisions
Stacey, D., Lewis, K. B., Smith, M. P., Carley, M. E., Volk, R. J., Douglas, E. E., Pacheco‐Brousseau, L., Finderup, J., Gunderson, J., Barry, M. J., et al. (2024) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd001431.pub6 · Cited by 398 · see citing works
O. B. O. T. C.-S. G., Grant, S., Mayo-Wilson, E., Montgomery, P., Macdonald, G., Michie, S., Hopewell, S., & Moher, D. (2018) · Trials · doi:10.1186/s13063-018-2735-z · Cited by 348 · see citing works
Self-citationBird, M., McGillion, M. H., Chambers, E., Dix, J., Fajardo, C., Gilmour, M., Levesque, K., Lim, A., Mierdel, S., Ouellette, C., et al. (2021) · Research Involvement and Engagement · doi:10.1186/s40900-021-00252-7 · Cited by 330 · see citing works
“End-user involvement is integral to the design, conduct, and analysis of the entire DigiComp Kids project, and is reported here according to the GRIPP2 Long Form Checklist [21] (Additional file 2).”
MethodBird, M., Ouellette, C., Whitmore, C., Li, L. H., Nair, K., McGillion, M. H., Yost, J., Banfield, L. E., Campbell, E., & Carroll, S. L. (2020) · Health Expectations · doi:10.1111/hex.13040 · Cited by 312 · see citing works
Smits, D.-W., van Meeteren, K., Klem, M., Alsem, M., & Ketelaar, M. (2020) · Research Involvement and Engagement · doi:10.1186/s40900-020-00188-4 · Cited by 295 · see citing works
“Recently international evidence based, consensus informed guidelines have been published for reporting PPI in research (Guidance for Reporting Involvement of Patients and the Public; GRIPP2), including minimum reporting requirements in a short form [43, 44].”
BackgroundPatient and public engagement in priority setting: A systematic rapid review of the literature
Manafò, E., Petermann, L., Vandall‐Walker, V., & Mason-Lai, P. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193579 · Cited by 289 · see citing works
Are you really doing ‘codesign’? Critical reflections when working with vulnerable populations
Moll, S. E., Wyndham‐West, M., Mulvale, G. M., Park, S., Buettgen, A., Phoenix, M. P., Fleisig, R. V., & Bruce, E. (2020) · BMJ Open · doi:10.1136/bmjopen-2020-038339 · Cited by 284 · see citing works
Carr, M., Steeg, S., Webb, R. T., Kapur, N., Chew-Graham, C. A., Abel, K. M., Hope, H. F., Pierce, M., & Ashcroft, D. M. (2021) · The Lancet Public Health · doi:10.1016/s2468-2667(20)30288-7 · Cited by 259 · see citing works
Petkovic, J., Riddle, A. Y., Akl, E. A., Khabsa, J., Lytvyn, L., Atwere, P., Campbell, P., Chalkidou, K., Chang, S., Crowe, S., et al. (2020) · Systematic Reviews · doi:10.1186/s13643-020-1272-5 · Cited by 241 · see citing works
Fineberg, N. A., Menchón, J. M., Hall, N., Dell’Osso, B. M., Brand, M., Potenza, M. N., Chamberlain, S. R., Cirnigliaro, G., Löchner, C., Billieux, J., et al. (2022) · Comprehensive Psychiatry · doi:10.1016/j.comppsych.2022.152346 · Cited by 253 · see citing works
Halvorsrud, K., Kucharska, J., Adlington, K., Rüdell, K., Hajdukova, E. B., Nazroo, J. Y., Haarmans, M., Rhodes, J., & Bhui, K. S. (2019) · Journal of Public Health · doi:10.1093/pubmed/fdz126 · Cited by 222 · see citing works
Staniszewska, S. H., Denegri, S., Matthews, R., & Minogue, V. (2018) · BMJ Open · doi:10.1136/bmjopen-2017-017124 · Cited by 211 · see citing works
Self-citationPatient and Public Engagement in Integrated Knowledge Translation Research: Are we there yet?
Banner, D., Bains, M., Carroll, S. L., Kandola, D. K., Rolfe, D. E., Wong, C., & Graham, I. D. (2019) · Research Involvement and Engagement · doi:10.1186/s40900-019-0139-1 · Cited by 214 · see citing works
Husereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E. W., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · Applied Health Economics and Health Policy · doi:10.1007/s40258-021-00704-x · Cited by 211 · see citing works
Self-citationEvaluating patient and public involvement in research
Boivin, A., Richards, T., Forsythe, L., Grégoire, A., L’Espérance, A., Abelson, J., & Carman, K. L. (2018) · BMJ · doi:10.1136/bmj.k5147 · Cited by 208 · see citing works
How to incorporate patient and public perspectives into the design and conduct of research
Hoddinott, P., Pollock, A., O’Cathain, A., Boyer, I., Taylor, J., MacDonald, C., Oliver, S. R., & Donovan, J. (2018) · F1000Research · doi:10.12688/f1000research.15162.1 · Cited by 207 · see citing works
CONSORT 2025 explanation and elaboration: updated guideline for reporting randomised trials
Hopewell, S., Chan, A.-W., Collins, G. S., Hróbjartsson, A., Moher, D., Schulz, K. F., Tunn, R., Aggarwal, R., Berkwits, M., Berlin, J. A., et al. (2025) · BMJ · doi:10.1136/bmj-2024-081124 · Cited by 205 · see citing works
Self-citationPollock, D., Alexander, L., Munn, Z., Peters, M. D. J., Khalil, H., Godfrey, C. M., McInerney, P. A., Synnot, A., & Tricco, A. C. (2022) · JBI Evidence Synthesis · doi:10.11124/jbies-21-00416 · Cited by 188 · see citing works
“ct need to report the aim of engagement; need to provide a clear description of the approach and process; ways the use of engagement with knowledge users affected on the interpretation of results; extent to which engagement influenced the overall study; and reflection/critical perspective of how engagement went as a l…”
BackgroundMethodThe prevalence of patient engagement in published trials: a systematic review
Fergusson, D. A., Monfaredi, Z., Pussegoda, K., Garritty, C., Lyddiatt, A., Shea, B., Duffett, L. D., Ghannad, M., Montroy, J. R., Murad, M. H., et al. (2018) · Research Involvement and Engagement · doi:10.1186/s40900-018-0099-x · Cited by 182 · see citing works
Stakeholder involvement in systematic reviews: a scoping review
Pollock, A., Campbell, P., Struthers, C., Synnot, A., Nunn, J., Hill, S., Goodare, H., Morris, J., Watts, C., & Morley, R. (2018) · Systematic Reviews · doi:10.1186/s13643-018-0852-0 · Cited by 180 · see citing works
“stakeholder involvement in research has recently been updated (GRIPP2, [62]); however, this guidance has not been specifically tested for use with systematic reviews and has lacked international input during development.”
BackgroundPatient and public involvement in research: a review of practical resources for young investigators
Arumugam, A., Phillips, L. R., Moore, A. P., Senthil Kumaran, D., Sampath, K. K., Migliorini, F., Maffulli, N., Ranganadhababu, B. N., Hegazy, F. A., & Bemden, A. B. (2023) · BMC Rheumatology · doi:10.1186/s41927-023-00327-w · Cited by 180 · see citing works
Jennings, H., Slade, M., Bates, P., Munday, E., & Toney, R. (2018) · BMC Psychiatry · doi:10.1186/s12888-018-1794-8 · Cited by 180 · see citing works
Role of patient and public involvement in implementation research: a consensus study
Gray‐Burrows, K. A., Willis, T. A., Foy, R., Rathfelder, M., Bland, P., Chin, A., Hodgson, S., Ibegbuna, G., Prestwich, G., Samuel, K., et al. (2018) · BMJ Quality & Safety · doi:10.1136/bmjqs-2017-006954 · Cited by 175 · see citing works
Patient engagement in research related to dementia: A scoping review
Bethell, J., Commisso, E., Rostad, H. M., Puts, M. T. E., Babineau, J., Grinbergs‐Saull, A., Wighton, M. B., Hammel, J., Doyle, E., Nadeau, S., et al. (2018) · Dementia · doi:10.1177/1471301218789292 · Cited by 177 · see citing works
Hollin, I., Craig, B. M., Coast, J., Beusterien, K., Vass, C., DiSantostefano, R., & Peay, H. (2019) · Patient · doi:10.1007/s40271-019-00401-x · Cited by 161 · see citing works
Current trends in patient and public involvement in cancer research: A systematic review
Pii, K. H., Schou, L., Piil, K., & Jarden, M. (2018) · Health Expectations · doi:10.1111/hex.12841 · Cited by 168 · see citing works
Blackburn, S. J., McLachlan, S., Jowett, S. M., Kinghorn, P., Gill, P. S., Higginbottom, A., Rhodes, C., Stevenson, F. A., & Jinks, C. (2018) · Research Involvement and Engagement · doi:10.1186/s40900-018-0100-8 · Cited by 165 · see citing works
Price, A. I., Schroter, S., Snow, R., Hicks, M. D., Harmston, R., Staniszewska, S. H., Parker, S., & Richards, T. (2018) · BMJ Open · doi:10.1136/bmjopen-2017-020452 · Cited by 155 · see citing works
Self-citationStaley, K., & Barron, D. (2019) · Research Involvement and Engagement · doi:10.1186/s40900-019-0147-1 · Cited by 157 · see citing works
Boylan, A. R., Locock, L., Thomson, R., & Staniszewska, S. H. (2019) · Health Expectations · doi:10.1111/hex.12883 · Cited by 154 · see citing works
Self-citationAttitudes and approaches to patient and public involvement across Europe: A systematic review
Biddle, M. S. Y., Gibson, A., & Evans, D. (2020) · Health & Social Care in the Community · doi:10.1111/hsc.13111 · Cited by 152 · see citing works
Husereau, D., Drummond, M., Augustovski, F., Briggs, A., Carswell, C., Caulley, L., Chaiyakunapruk, N., de Bekker‐Grob, E., Greenberg, D., Loder, E., et al. (2022) · BJOG: An International Journal of Obstetrics & Gynaecology · doi:10.1111/1471-0528.17012 · Cited by 150 · see citing works
Self-citationHusereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E. W., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · MDM Policy & Practice · doi:10.1177/23814683211061097 · Cited by 149 · see citing works
Self-citationCalvert, M., King, M. T., Mercieca‐Bebber, R., Aiyegbusi, O. L., Kyte, D. G., Slade, A. L., Chan, A., Basch, E., Bell, J. A., Bennett, A. V., et al. (2021) · BMJ Open · doi:10.1136/bmjopen-2020-045105 · Cited by 140 · see citing works
What constitutes meaningful engagement for patients and families as partners on research teams?
Black, A., Strain, K., Wallsworth, C., Charlton, S.-G., Chang, W., McNamee, K., & Hamilton, C. B. (2018) · Journal of Health Services Research & Policy · doi:10.1177/1355819618762960 · Cited by 134 · see citing works
Hamilton, C. B., Hoens, A. M., McQuitty, S., McKinnon, A., English, K., Backman, C. L., Azimi, T., Khodarahmi, N., & LI, L. C. (2018) · PLoS ONE · doi:10.1371/journal.pone.0206588 · Cited by 133 · see citing works
Patient and public involvement in dementia research in the European Union: a scoping review
Miah, J., Dawes, P., Edwards, S., Leroi, I., Starling, B., & Parsons, S. (2019) · BMC Geriatrics · doi:10.1186/s12877-019-1217-9 · Cited by 133 · see citing works
“In the present study, we adapted the GRIPP2 by adding two sections to describe the method of evaluation of the impact of PPI (if included) and what the reported impacts of PPI were.”
BackgroundMethodInfluentialYoung people’s advisory groups in health research: scoping review and mapping of practices
Sellars, E., Pavarini, G., Michelson, D., Creswell, C., & Fazel, M. S. (2020) · Archives of Disease in Childhood · doi:10.1136/archdischild-2020-320452 · Cited by 132 · see citing works
d’Elia, A., Gabbay, M., Rodgers, S., Kierans, C., Jones, E., Durrani, I., Thomas, A., & Frith, L. (2022) · Family Medicine and Community Health · doi:10.1136/fmch-2022-001670 · Cited by 129 · see citing works
Cook, N., Siddiqi, N., Twiddy, M., & KENYON, R. L. (2019) · BMJ Open · doi:10.1136/bmjopen-2018-026514 · Cited by 124 · see citing works
Modigh, A., Sampaio, F., Moberg, L., & Fredriksson, M. (2021) · Health Policy · doi:10.1016/j.healthpol.2021.07.008 · Cited by 123 · see citing works
Guidance on authorship with and acknowledgement of patient partners in patient-oriented research
Richards, D. P., Birnie, K. A., Eubanks, K., Lane, T., Linkiewich, D., Singer, L. N., Stinson, J., & Begley, K. N. (2020) · Research Involvement and Engagement · doi:10.1186/s40900-020-00213-6 · Cited by 118 · see citing works
“to a research project, as well as for these roles to be appropriately acknowledged and reflected in the resulting scientific literature [11, 12].”
BackgroundPeters, S., Guccione, L., Francis, J., Best, S., Tavender, E. J., Curran, J., Davies, K., Rowe, S., Palmer, V. J., & Klaic, M. (2024) · Implementation Science · doi:10.1186/s13012-024-01394-4 · Cited by 135 · see citing works
Doria, N. A., Condran, B. R., Boulos, L., Maillet, D. C., Dowling, L., & Levy, A. R. (2018) · Research Involvement and Engagement · doi:10.1186/s40900-018-0102-6 · Cited by 115 · see citing works
Making Pain Research More Inclusive: Why and How
Janevic, M. R., Mathur, V. A., Booker, S. Q., Moraís, C. A., Meints, S. M., Yeager, K. A., & Meghani, S. H. (2021) · Journal of Pain · doi:10.1016/j.jpain.2021.10.004 · Cited by 119 · see citing works
Service user's actual involvement in mental health research practices: A scoping review
Sangill, C., Buus, N., Hybholt, L., & Berring, L. L. (2019) · International Journal of Mental Health Nursing · doi:10.1111/inm.12594 · Cited by 112 · see citing works
Benz, C., Scott-Jeffs, W., McKercher, K. A., Welsh, M., Norman, R., Hendrie, D. V., Locantro, M., & Robinson, S. (2024) · Research Involvement and Engagement · doi:10.1186/s40900-024-00573-3 · Cited by 112 · see citing works
“The reporting of this article has been completed in line with the Guidance for Reporting Involvement of Patients and the Public (GRIPP2) checklist [7].”
Rouncefield‐Swales, A., Harris, J., Carter, B., Bray, L., Bewley, T., & Martin, R. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252774 · Cited by 115 · see citing works
Mathie, E., Wythe, H., Munday, D., Millac, P. A. H., Rhodes, G., Roberts, N., Smeeton, N., Poland, F. M., & Jones, J. (2018) · Health Expectations · doi:10.1111/hex.12684 · Cited by 103 · see citing works
Skovlund, P. C., Nielsen, B. K., Thaysen, H. V., Schmidt, H., Finset, A., Hansen, K. A., & Lomborg, K. E. (2020) · Research Involvement and Engagement · doi:10.1186/s40900-020-00214-5 · Cited by 103 · see citing works
Key issues in co-creation with stakeholders when research problems are complex
Bammer, G. (2019) · Evidence & Policy · doi:10.1332/174426419x15532579188099 · Cited by 100 · see citing works
Patient and Public Involvement in research: A journey to co-production
Price, A., Clarke, M., Staniszewska, S., Chu, L., Tembo, D., Kirkpatrick, M., & Nelken, Y. (2022) · Patient Education and Counseling · doi:10.1016/j.pec.2021.07.021 · Cited by 90 · see citing works
Self-citationRoche, P. L., Shimmin, C., Hickes, S., Khan, M., Sherzoi, O., Wicklund, E. D., Lavoie, J. G., Hardie, S., Wittmeier, K. D. M., & Sibley, K. M. (2020) · Research Involvement and Engagement · doi:10.1186/s40900-020-00217-2 · Cited by 96 · see citing works
Husereau, D., Drummond, M., Augustovski, F., de Bekker-Grob, E. W., Briggs, A. H., Carswell, C., Caulley, L., Chaiyakunapruk, N., Greenberg, D., Loder, E., et al. (2022) · PharmacoEconomics · doi:10.1007/s40273-021-01112-8 · Cited by 95 · see citing works
“A completed Guidance for Reporting Involvement of Patients and the Public—version 2 (GRIPP2) [42] checklist is in Appendix A in the electronic supplementary material (ESM).”
BackgroundSelf-citationAgyei‐Manu, E., Atkins, N., Lee, B., Rostron, J., Dozier, M., Smith, M. P., & McQuillan, R. (2023) · Health Expectations · doi:10.1111/hex.13787 · Cited by 99 · see citing works
Dawson, S., Ruddock, A., Parmar, V., Morris, R., Cheraghi‐Sohi, S., Giles, S. J., & Campbell, S. (2020) · Research Involvement and Engagement · doi:10.1186/s40900-020-00201-w · Cited by 90 · see citing works
“In line with the reporting recommendations in Guidance for Reporting Involvement of Patients and the Public (GRIPP2) short form [39], we have reported on all aspects of the processes involved in undertaking PPI.”
MethodElsman, E. B. M., Mokkink, L. B., Terwee, C. B., Beaton, D., Gagnier, J. J., Tricco, A. C., Baba, A., Butcher, N. J., Smith, M., Hofstetter, C., et al. (2024) · Quality of Life Research · doi:10.1007/s11136-024-03634-y · Cited by 96 · see citing works
Self-citationPatient and public involvement in designing and conducting doctoral research: the whys and the hows
Tomlinson, J., Medlinskiene, K., Cheong, V., Khan, S., & Fylan, B. (2019) · Research Involvement and Engagement · doi:10.1186/s40900-019-0155-1 · Cited by 87 · see citing works
Deane, K. H., Delbecque, L., Gorbenko, O., Hamoir, A.-M., Hoos, A., Nafría, B., Pakarinen, C., Sargeant, I., Richards, D. P., Skovlund, S. E., et al. (2019) · BMJ Innovations · doi:10.1136/bmjinnov-2018-000317 · Cited by 88 · see citing works
Reed, H., Couturiaux, D., Davis, M., Edwards, A., Janes, E. H., Kim, H. S., Meléndez‐Torres, G. J., Murphy, S., Rotevatn, T. A., Smith, J. L., et al. (2020) · Prevention Science · doi:10.1007/s11121-020-01182-8 · Cited by 87 · see citing works
Patient engagement in preclinical laboratory research: A scoping review
Fox, G., Fergusson, D. A., Daham, Z., Youssef, M., Foster, M., Poole, E., Sharif, A., Richards, D. P., Hendrick, K., Mendelson, A. A., et al. (2021) · EBioMedicine · doi:10.1016/j.ebiom.2021.103484 · Cited by 83 · see citing works
“The extraction form was developed with input from all team members and the GRIPP2 checklist [11].”
BackgroundMethodAn umbrella review on how digital health intervention co-design is conducted and described
Kilfoy, A., Hsu, T. C., Stockton-Powdrell, C., Whelan, P., Chu, C. H., & Jibb, L. (2024) · npj Digital Medicine · doi:10.1038/s41746-024-01385-1 · Cited by 98 · see citing works
Holland, E., Matthews, K., Macdonald, S., Ashworth, M. J., Laidlaw, L., Cheung, K. S. Y., Stannard, S., Francis, N. A., Mair, F. S., Rajababoo, R., et al. (2024) · BMC Public Health · doi:10.1186/s12889-024-20763-8 · Cited by 90 · see citing works
Briggs, A. M., Schneider, C. H., Slater, H., Jordan, J. E., Parambath, S., Young, J. J., Sharma, S., Kopansky-Giles, D. R., Mishrra, S., Åkesson, K., et al. (2021) · BMJ Global Health · doi:10.1136/bmjgh-2021-006045 · Cited by 83 · see citing works
Public Involvement in Global Genomics Research: A Scoping Review
Nunn, J., Tiller, J. M., Fransquet, P., & Lacaze, P. A. (2019) · Frontiers in Public Health · doi:10.3389/fpubh.2019.00079 · Cited by 78 · see citing works
Considerations for patient and public involvement and engagement in health research
Aiyegbusi, O. L., McMullan, C., Hughes, S., Turner, G., Subramanian, A., Hotham, R., Davies, E. H., Frost, C., Alder, Y., Agyen, L., et al. (2023) · Nature Medicine · doi:10.1038/s41591-023-02445-x · Cited by 81 · see citing works
The importance of measuring the impact of patient-oriented research
Aubin, D., Hebert, M., & Eurich, D. T. (2019) · Canadian Medical Association Journal · doi:10.1503/cmaj.190237 · Cited by 82 · see citing works
Jones, J., Cowe, M., Marks, S. A., McAllister, T., Mendoza, A., Ponniah, C., Wythe, H., & Mathie, E. (2021) · Research Involvement and Engagement · doi:10.1186/s40900-021-00295-w · Cited by 78 · see citing works
“In January 2018 the four co-researchers met with the lead researcher (JJ) to discuss the proposed review process using the GRIPP2 forms (Guidance for Reporting Involvement of Patients and the Public, version 2), which had recently been published [30].”
BackgroundMethodInfluentialStudy Protocol for “Psilocybin as a Treatment for Anorexia Nervosa: A Pilot Study”
Spriggs, M. J., Douglass, H. M., Park, R. J., Read, T., Danby, J. L., de Magalhães, F. J. C., Alderton, K. L., Williams, T. M., Blemings, A., Lafrance, A., et al. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.735523 · Cited by 75 · see citing works
Mann, C., Chilcott, S., PLUMB, K. H. M., Brooks, E., & Man, M. (2018) · Research Involvement and Engagement · doi:10.1186/s40900-018-0098-y · Cited by 77 · see citing works
Fox, S., BROWN, L. J. E., Antrobus, S., Brough, D., Drake, R., Jury, F., Leroi, I., Parry‐Jones, A., & Machin, M. (2021) · JMIR mhealth and uhealth · doi:10.2196/24483 · Cited by 70 · see citing works
Stakeholder engagement to inform HIV clinical trials: a systematic review of the evidence
Day, S., Blumberg, M., Vu, T. H., Zhao, Y., Rennie, S., & Tucker, J. D. (2018) · Journal of the International AIDS Society · doi:10.1002/jia2.25174 · Cited by 70 · see citing works
“criteria adapted from the GRIPP2 checklist to improve reporting of stakeholder involvement in health research [21].”
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Tailored physical activity behavior change interventions: challenges and opportunities
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“This could be integrated as part of the “people involved” section of the long-form GRIPP2 tool for reporting patient involvement [92].”
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“The development of the short and long form checklists both aim to improve the quality, transparency and consistency of the reporting of PI [47].”
BackgroundSelf-citationScoping review of models and frameworks of patient engagement in health services research
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- Authors
- Staniszewska, S., Brett, J., Simera, I., Seers, K., Mockford, C., Goodlad, S., Altman, D. G., Moher, D., Barber, R., Denegri, S., Entwistle, A., Littlejohns, P., Morris, C., Suleman, R., Thomas, V., & Tysall, C.
- Affiliations
- University of Warwick (GB)
- Oxford Brookes University (GB)
- University of Oxford (GB)
- Coventry University (GB)
- Ottawa Hospital Research Institute (CA)
- University of Sheffield (GB)
- National Institute for Health and Care Research (GB)
- King's College London (GB)
- University of Exeter (GB)
- National Institute for Health and Care Excellence (GB)
- Corresponding author
- Staniszewska, S.
- ORCID
- Venue
- Research Involvement and Engagement
- Published
- 2017-08-02
- Volume
- 3
- Issue
- 1
- Pages
- 13-13
- ISSN
- 2056-7529 (ISSN-L)
- PMC
- PMC5611595
- OpenAlex
- W2739751169
- Semantic Scholar
- a636c43b2bfbe8ccca687ee5309af8ef920128fa
- Cited by
- 1,643
- References
- 20
- Citations by year
- 2026: 98 · 2025: 192 · 2024: 327 · 2023: 265 · 2022: 238 · 2021: 211 · 2020: 145 · 2019: 95 · 2018: 61 · 2017: 8
- FWCI
- 136.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Research Involvement and Engagement (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by-nc)
- Figshare (submittedVersion)
- Open Research Exeter (University of Exeter) (submittedVersion, cc-by)
- Radar (Oxford Brookes University) (submittedVersion, cc-by)
- Funders
- King's College Hospital NHS Foundation Trust
- Cancer Research UK (16895)
- National Institute for Health and Care Research
- University of Warwick
- King's College London
- Warwick Medical School
- Topics
- Health Sciences › Health Professions › General Health Professions › Mental Health and Patient Involvement
- Health Sciences › Health Professions › General Health Professions › Health Policy Implementation Science
- Social Sciences › Decision Sciences › Statistics, Probability and Uncertainty › Meta-analysis and systematic reviews
- Keywords
- patient and public involvement, reporting guidelines, GRIPP2, reporting checklist, research collaboration, patient involvement in research, Delphi consensus, EQUATOR Network, research transparency
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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