Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation

Abstract Background There is limited evidence for the impact of involving patients and the public (PPI) in health research. Descriptions of the PPI process are seldom included in publications, particularly data analysis, yet an understanding of processes and impacts of PPI is essential if its contri...

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Main Authors: Rachel Stocker, Katie Brittain, Karen Spilsbury, Barbara Hanratty
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Health Expectations
Subjects:
Online Access:https://doi.org/10.1111/hex.13269
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spelling doaj-61f424c3ed3f4001bb06c0f33b1f10aa2021-08-17T05:09:01ZengWileyHealth Expectations1369-65131369-76252021-08-012441349135610.1111/hex.13269Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretationRachel Stocker0Katie Brittain1Karen Spilsbury2Barbara Hanratty3Population Health Sciences Institute Newcastle University Newcastle upon Tyne UKPopulation Health Sciences Institute Newcastle University Newcastle upon Tyne UKSchool of Healthcare University of Leeds Leeds UKPopulation Health Sciences Institute Newcastle University Newcastle upon Tyne UKAbstract Background There is limited evidence for the impact of involving patients and the public (PPI) in health research. Descriptions of the PPI process are seldom included in publications, particularly data analysis, yet an understanding of processes and impacts of PPI is essential if its contribution to research is to be evaluated. Objective To describe the ‘how’ of PPI in qualitative data analysis and critically reflect on potential impact. Methods We focus on the development and critical reflection of our step‐by‐step approach to collaborative qualitative data analysis (through a series of analysis workshops) in a specific care home study, and our long‐term engagement model with patients and the public (termed PPI partners). Results An open access PPI group, with multiple events over time, sustained broad interest in care home research. Recordings of interview clips, role‐play of interview excerpts and written theme summaries were used in workshops to facilitate PPI partner engagement with data analysis in a specific study. PPI resulted in changes to data interpretation and was perceived to make the research process accessible. We reflect on the challenge of judging the benefits of PPI and presenting PPI in research publications for critical commentary. Conclusions Patient and public involvement partners who are actively engaged with data analysis can positively influence research studies. However, guidance for researchers is needed on approaches to PPI, including appropriate levels and methods for evaluation. Without more systematic approaches, we argue that it is impossible to know whether PPI represents good use of resources and is generating a real impact.https://doi.org/10.1111/hex.13269community participationlong‐term care facilitiespatient and public involvementqualitative researchresearch design
collection DOAJ
language English
format Article
sources DOAJ
author Rachel Stocker
Katie Brittain
Karen Spilsbury
Barbara Hanratty
spellingShingle Rachel Stocker
Katie Brittain
Karen Spilsbury
Barbara Hanratty
Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
Health Expectations
community participation
long‐term care facilities
patient and public involvement
qualitative research
research design
author_facet Rachel Stocker
Katie Brittain
Karen Spilsbury
Barbara Hanratty
author_sort Rachel Stocker
title Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
title_short Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
title_full Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
title_fullStr Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
title_full_unstemmed Patient and public involvement in care home research: Reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
title_sort patient and public involvement in care home research: reflections on the how and why of involving patient and public involvement partners in qualitative data analysis and interpretation
publisher Wiley
series Health Expectations
issn 1369-6513
1369-7625
publishDate 2021-08-01
description Abstract Background There is limited evidence for the impact of involving patients and the public (PPI) in health research. Descriptions of the PPI process are seldom included in publications, particularly data analysis, yet an understanding of processes and impacts of PPI is essential if its contribution to research is to be evaluated. Objective To describe the ‘how’ of PPI in qualitative data analysis and critically reflect on potential impact. Methods We focus on the development and critical reflection of our step‐by‐step approach to collaborative qualitative data analysis (through a series of analysis workshops) in a specific care home study, and our long‐term engagement model with patients and the public (termed PPI partners). Results An open access PPI group, with multiple events over time, sustained broad interest in care home research. Recordings of interview clips, role‐play of interview excerpts and written theme summaries were used in workshops to facilitate PPI partner engagement with data analysis in a specific study. PPI resulted in changes to data interpretation and was perceived to make the research process accessible. We reflect on the challenge of judging the benefits of PPI and presenting PPI in research publications for critical commentary. Conclusions Patient and public involvement partners who are actively engaged with data analysis can positively influence research studies. However, guidance for researchers is needed on approaches to PPI, including appropriate levels and methods for evaluation. Without more systematic approaches, we argue that it is impossible to know whether PPI represents good use of resources and is generating a real impact.
topic community participation
long‐term care facilities
patient and public involvement
qualitative research
research design
url https://doi.org/10.1111/hex.13269
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