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      Reciprocal relationships and the importance of feedback in patient and public involvement: A mixed methods study

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          Abstract

          Background

          Reciprocal relationships between researchers and patient and public involvement ( PPI) contributors can enable successful PPI in research. However, research and anecdotal evidence suggest that researchers do not commonly provide feedback to PPI contributors thus preventing them from knowing whether, how or where their contributions were useful to researchers and research overall.

          Aims

          The aim of this study was to explore the variation, types, importance of, and satisfaction with feedback given by researchers to PPI contributors in six PPI groups in England, and identify the barriers to the process of feedback.

          Methods

          An explanatory mixed methods sequential study design with a questionnaire survey followed by semi‐structured interviews with researchers and PPI contributors in six PPI groups. PPI contributors were involved in all stages of the research process.

          Results

          Researchers do not routinely give feedback to PPI contributors. Feedback was found to have different meanings: an acknowledgement, impact and study success and progress. PPI contributors who receive feedback are motivated for further involvement; it supports their learning and development and prompts researchers to reflect on PPI impact. The importance of the role of a PPI lead or coordinator to facilitate the process of providing feedback was also highlighted.

          Conclusion

          This study found no generic way to give feedback indicating that mutual feedback expectations should be discussed at the outset. PPI feedback needs to become integral to the research process with appropriate time and resources allocated. PPI feedback can be seen as a key indicator of mature, embedded PPI in research.

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          Most cited references21

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          ReseArch with Patient and Public invOlvement: a RealisT evaluation – the RAPPORT study

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            Values associated with public involvement in health and social care research: a narrative review

            Abstract Background Much has been written about public involvement (PI) in health and social care research, but underpinning values are rarely made explicit despite the potential for these to have significant influence on the practice and assessment of PI. Objective The narrative review reported here is part of a larger MRC‐funded study which is producing a framework and related guidance on assessing the impact of PI in health and social care research. The review aimed to identify and characterize the range of values associated with PI that are central elements of the framework. Methods We undertook a review and narrative synthesis of diverse literatures of PI in health and social care research, including twenty existing reviews and twenty‐four chapters in sixteen textbooks. Results Three overarching value systems were identified, each containing five value clusters. (i) A system concerned with ethical and/or political issues including value clusters associated with empowerment; change/action; accountability/transparency; rights; and ethics (normative values). (ii). A system concerned with the consequences of public involvement in research including value clusters associated with effectiveness; quality/relevance; validity/reliability; representativeness/objectivity/generalizability; and evidence (substantive values). (iii) A system concerned with the conduct of public involvement in including value clusters associated with Partnership/equality; respect/trust; openness and honesty; independence; and clarity (process values). Conclusion Our review identified three systems associated with PI in health and social care research focused on normative, substantive and process values. The findings suggest that research teams should consider and make explicit the values they attach to PI in research and discuss ways in which potential tensions may be managed in order to maximize the benefits of PI for researchers, lay experts and the research.
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              PPI, paradoxes and Plato: who's sailing the ship?

              Over the last decade, patient and public involvement (PPI) has become a requisite in applied health research. Some funding bodies demand explicit evidence of PPI, while others have made a commitment to developing PPI in the projects they fund. Despite being commonplace, there remains a dearth of engagement with the ethical and theoretical underpinnings of PPI processes and practices. More specifically, while there is a small (but growing) body of literature examining the effectiveness and impact of PPI, there has been relatively little reflection on whether the concept/practice of PPI is internally coherent. Here, the authors unpick a 'paradox' within PPI, which highlights a tension between its moral and pragmatic motivations and its implementation. The authors argue that this 'professionalisation paradox' means we need to rethink the practice, and purpose, of PPI in research.
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                Author and article information

                Contributors
                E.J.Mathie@herts.ac.uk
                Journal
                Health Expect
                Health Expect
                10.1111/(ISSN)1369-7625
                HEX
                Health Expectations : An International Journal of Public Participation in Health Care and Health Policy
                John Wiley and Sons Inc. (Hoboken )
                1369-6513
                1369-7625
                14 April 2018
                October 2018
                : 21
                : 5 ( doiID: 10.1111/hex.2018.21.issue-5 )
                : 899-908
                Affiliations
                [ 1 ] CRIPACC University of Hertfordshire Hatfield UK
                [ 2 ] Public Involvement in Research Group CRIPACC University of Hertfordshire Hatfield UK
                [ 3 ] INsPIRE Patient and Public Involvement in Research Bedfordshire and Peterborough UK
                [ 4 ] School of Health Science University of East Anglia Norwich UK
                Author notes
                [*] [* ] Correspondence

                Elspeth Mathie, CRIPACC, College Lane, University of Hertfordshire, Hatfield, UK.

                Email: E.J.Mathie@ 123456herts.ac.uk

                Author information
                http://orcid.org/0000-0002-5871-436X
                Article
                HEX12684
                10.1111/hex.12684
                6186542
                29654644
                89592ebb-6c2a-4815-871c-b6618bae6481
                © 2018 The Author. Health Expectations published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 16 February 2018
                Page count
                Figures: 0, Tables: 6, Pages: 10, Words: 8050
                Funding
                Funded by: National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research & Care (CLAHRC) East of England
                Categories
                Original Research Paper
                Original Research Papers
                Custom metadata
                2.0
                hex12684
                October 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.0.1 mode:remove_FC converted:14.10.2018

                Health & Social care
                feedback,health,patient and public involvement,public,research
                Health & Social care
                feedback, health, patient and public involvement, public, research

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