GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research
Abstract Background 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. Objective To develop international consens...
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doaj-644b147cfd9e43fbb182909d62d960152020-11-25T00:34:25ZengBMCResearch Involvement and Engagement2056-75292017-08-013111110.1186/s40900-017-0062-2GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in researchS. Staniszewska0J. Brett1I. Simera2K. Seers3C. Mockford4S. Goodlad5D. G. Altman6D. Moher7R. Barber8S. Denegri9A. Entwistle10P. Littlejohns11C. Morris12R. Suleman13V. Thomas14C. Tysall15Warwick Research in Nursing, Warwick Medical School, University of WarwickFaculty of Health and Life Sciences, Oxford Brookes UniversityCentre for Tropical Medicine and Global Health and UK EQUATOR Centre, University of OxfordWarwick Research in Nursing, Warwick Medical School, University of WarwickWarwick Medical SchoolCoventry UniversityCentre for Statistics in Medicine, University of OxfordCentre for Journalology, Clinical Epidemiology Program, Ottawa Hospital Research InstituteSchool of Health and Related Research, University of SheffieldNational Institute for Health Research, UCL School of Life and Medical SciencesWarwick Medical SchoolKings College LondonUniversity of Exeter Medical SchoolWarwick Medical SchoolPublic Involvement Programme, National Institute for Health and Care ExcellenceWarwick Medical SchoolAbstract Background 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. Objective 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. Methods 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. Results 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. Conclusions 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.http://link.springer.com/article/10.1186/s40900-017-0062-2 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Staniszewska J. Brett I. Simera K. Seers C. Mockford S. Goodlad D. G. Altman D. Moher R. Barber S. Denegri A. Entwistle P. Littlejohns C. Morris R. Suleman V. Thomas C. Tysall |
spellingShingle |
S. Staniszewska J. Brett I. Simera K. Seers C. Mockford S. Goodlad D. G. Altman D. Moher R. Barber S. Denegri A. Entwistle P. Littlejohns C. Morris R. Suleman V. Thomas C. Tysall GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research Research Involvement and Engagement |
author_facet |
S. Staniszewska J. Brett I. Simera K. Seers C. Mockford S. Goodlad D. G. Altman D. Moher R. Barber S. Denegri A. Entwistle P. Littlejohns C. Morris R. Suleman V. Thomas C. Tysall |
author_sort |
S. Staniszewska |
title |
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research |
title_short |
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research |
title_full |
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research |
title_fullStr |
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research |
title_full_unstemmed |
GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research |
title_sort |
gripp2 reporting checklists: tools to improve reporting of patient and public involvement in research |
publisher |
BMC |
series |
Research Involvement and Engagement |
issn |
2056-7529 |
publishDate |
2017-08-01 |
description |
Abstract Background 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. Objective 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. Methods 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. Results 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. Conclusions 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. |
url |
http://link.springer.com/article/10.1186/s40900-017-0062-2 |
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