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Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study

OBJECTIVE: There is growing interest in the potential benefits of public involvement (PI) in health and social care research. However, there has been little examination of values underpinning PI or how these values might differ for different groups with an interest in PI in the research process. We...

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Autores principales: Snape, D, Kirkham, J, Preston, J, Popay, J, Britten, N, Collins, M, Froggatt, K, Gibson, A, Lobban, F, Wyatt, K, Jacoby, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902382/
https://www.ncbi.nlm.nih.gov/pubmed/24413356
http://dx.doi.org/10.1136/bmjopen-2013-004217
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author Snape, D
Kirkham, J
Preston, J
Popay, J
Britten, N
Collins, M
Froggatt, K
Gibson, A
Lobban, F
Wyatt, K
Jacoby, A
author_facet Snape, D
Kirkham, J
Preston, J
Popay, J
Britten, N
Collins, M
Froggatt, K
Gibson, A
Lobban, F
Wyatt, K
Jacoby, A
author_sort Snape, D
collection PubMed
description OBJECTIVE: There is growing interest in the potential benefits of public involvement (PI) in health and social care research. However, there has been little examination of values underpinning PI or how these values might differ for different groups with an interest in PI in the research process. We aimed to explore areas of consensus and conflict around normative, substantive and process-related values underpinning PI. DESIGN: Mixed method, three-phase, modified Delphi study, conducted as part of a larger multiphase project. SETTING: The UK health and social care research community. PARTICIPANTS: Stakeholders in PI in research, defined as: clinical and non-clinical academics, members of the public, research managers, commissioners and funders; identified via research networks, online searches and a literature review. RESULTS: We identified high levels of consensus for many normative, substantive and process-related issues. However, there were also areas of conflict in relation to issues of bias and representativeness, and around whether the purpose of PI in health and social care research is to bring about service change or generate new knowledge. There were large differences by group in the percentages endorsing the ethical justification for PI and the argument that PI equalises power imbalances. With regard to practical implementation of PI, research support infrastructures were reported as lacking. Participants reported shortcomings in the uptake and practice of PI. Embedding PI practice and evaluation in research study designs was seen as fundamental to strengthening the evidence base. CONCLUSIONS: Our findings highlight the extent to which PI is already embedded in research. However, they also highlight a need for ‘best practice’ standards to assist research teams to understand, implement and evaluate PI. These findings have been used in developing a Public Involvement Impact Assessment Framework (PiiAF), which offers guidance to researchers and members of the public involved in the PI process.
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spelling pubmed-39023822014-01-27 Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study Snape, D Kirkham, J Preston, J Popay, J Britten, N Collins, M Froggatt, K Gibson, A Lobban, F Wyatt, K Jacoby, A BMJ Open Health Services Research OBJECTIVE: There is growing interest in the potential benefits of public involvement (PI) in health and social care research. However, there has been little examination of values underpinning PI or how these values might differ for different groups with an interest in PI in the research process. We aimed to explore areas of consensus and conflict around normative, substantive and process-related values underpinning PI. DESIGN: Mixed method, three-phase, modified Delphi study, conducted as part of a larger multiphase project. SETTING: The UK health and social care research community. PARTICIPANTS: Stakeholders in PI in research, defined as: clinical and non-clinical academics, members of the public, research managers, commissioners and funders; identified via research networks, online searches and a literature review. RESULTS: We identified high levels of consensus for many normative, substantive and process-related issues. However, there were also areas of conflict in relation to issues of bias and representativeness, and around whether the purpose of PI in health and social care research is to bring about service change or generate new knowledge. There were large differences by group in the percentages endorsing the ethical justification for PI and the argument that PI equalises power imbalances. With regard to practical implementation of PI, research support infrastructures were reported as lacking. Participants reported shortcomings in the uptake and practice of PI. Embedding PI practice and evaluation in research study designs was seen as fundamental to strengthening the evidence base. CONCLUSIONS: Our findings highlight the extent to which PI is already embedded in research. However, they also highlight a need for ‘best practice’ standards to assist research teams to understand, implement and evaluate PI. These findings have been used in developing a Public Involvement Impact Assessment Framework (PiiAF), which offers guidance to researchers and members of the public involved in the PI process. BMJ Publishing Group 2014-01-10 /pmc/articles/PMC3902382/ /pubmed/24413356 http://dx.doi.org/10.1136/bmjopen-2013-004217 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/3.0/
spellingShingle Health Services Research
Snape, D
Kirkham, J
Preston, J
Popay, J
Britten, N
Collins, M
Froggatt, K
Gibson, A
Lobban, F
Wyatt, K
Jacoby, A
Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title_full Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title_fullStr Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title_full_unstemmed Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title_short Exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified Delphi study
title_sort exploring areas of consensus and conflict around values underpinning public involvement in health and social care research: a modified delphi study
topic Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902382/
https://www.ncbi.nlm.nih.gov/pubmed/24413356
http://dx.doi.org/10.1136/bmjopen-2013-004217
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