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A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study
BACKGROUND: Patient and public involvement (PPI) is increasingly seen as essential to health service research. There are strong moral and ethical arguments for good quality PPI. Despite the development of guidance aimed at addressing the inconsistent reporting of PPI activities within research, litt...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233873/ https://www.ncbi.nlm.nih.gov/pubmed/37259130 http://dx.doi.org/10.1186/s40900-023-00440-7 |
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author | Moult, Alice McGrath, Carmel Lippiett, Kate Coope, Caroline Chilcott, Simon Mann, Cindy Evans, Nicola Turner, Andrew Dziedzic, Krysia Portillo, M. C. Johnson, Rachel |
author_facet | Moult, Alice McGrath, Carmel Lippiett, Kate Coope, Caroline Chilcott, Simon Mann, Cindy Evans, Nicola Turner, Andrew Dziedzic, Krysia Portillo, M. C. Johnson, Rachel |
author_sort | Moult, Alice |
collection | PubMed |
description | BACKGROUND: Patient and public involvement (PPI) is increasingly seen as essential to health service research. There are strong moral and ethical arguments for good quality PPI. Despite the development of guidance aimed at addressing the inconsistent reporting of PPI activities within research, little progress has been made in documenting the steps taken to undertake PPI and how it influences the direction of a study. Without this information, there are minimal opportunities to share learnings across projects and strengthen future PPI practices. The aim of this paper is to present details on the processes and activities planned to integrate PPI into the qualitative research component of a mixed-methods, multi-site study evaluating the implementation of a smart template to promote personalised primary care for patients with multiple long-term conditions. METHODS: This proposal describes the processes and activities planned to integrate PPI into the development and piloting of qualitative data collection tools (topic guides for both practice staff and patients) and a tailored data analysis package developed for PPI members incorporating broad concepts and specific methods of qualitative data analysis. DISCUSSION: Outputs relating to PPI activity may include clear, concise and suitably worded topic guides for qualitative interviews. Piloting of the topic guides via mock interviews will further develop researchers’ skills including sensitisation to the experiences of participants being interviewed. Working with PPI members when analysing the qualitative data aims to provide reciprocal learning opportunities and may contribute to improving the overall rigour of the data analysis. The intent of publishing proposed PPI activities within this project is to inform the future delivery of high quality PPI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40900-023-00440-7. |
format | Online Article Text |
id | pubmed-10233873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-102338732023-06-02 A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study Moult, Alice McGrath, Carmel Lippiett, Kate Coope, Caroline Chilcott, Simon Mann, Cindy Evans, Nicola Turner, Andrew Dziedzic, Krysia Portillo, M. C. Johnson, Rachel Res Involv Engagem Protocol BACKGROUND: Patient and public involvement (PPI) is increasingly seen as essential to health service research. There are strong moral and ethical arguments for good quality PPI. Despite the development of guidance aimed at addressing the inconsistent reporting of PPI activities within research, little progress has been made in documenting the steps taken to undertake PPI and how it influences the direction of a study. Without this information, there are minimal opportunities to share learnings across projects and strengthen future PPI practices. The aim of this paper is to present details on the processes and activities planned to integrate PPI into the qualitative research component of a mixed-methods, multi-site study evaluating the implementation of a smart template to promote personalised primary care for patients with multiple long-term conditions. METHODS: This proposal describes the processes and activities planned to integrate PPI into the development and piloting of qualitative data collection tools (topic guides for both practice staff and patients) and a tailored data analysis package developed for PPI members incorporating broad concepts and specific methods of qualitative data analysis. DISCUSSION: Outputs relating to PPI activity may include clear, concise and suitably worded topic guides for qualitative interviews. Piloting of the topic guides via mock interviews will further develop researchers’ skills including sensitisation to the experiences of participants being interviewed. Working with PPI members when analysing the qualitative data aims to provide reciprocal learning opportunities and may contribute to improving the overall rigour of the data analysis. The intent of publishing proposed PPI activities within this project is to inform the future delivery of high quality PPI. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40900-023-00440-7. BioMed Central 2023-05-31 /pmc/articles/PMC10233873/ /pubmed/37259130 http://dx.doi.org/10.1186/s40900-023-00440-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Protocol Moult, Alice McGrath, Carmel Lippiett, Kate Coope, Caroline Chilcott, Simon Mann, Cindy Evans, Nicola Turner, Andrew Dziedzic, Krysia Portillo, M. C. Johnson, Rachel A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title | A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title_full | A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title_fullStr | A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title_full_unstemmed | A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title_short | A proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
title_sort | proposal to embed patient and public involvement within qualitative data collection and analysis phases of a primary care based implementation study |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10233873/ https://www.ncbi.nlm.nih.gov/pubmed/37259130 http://dx.doi.org/10.1186/s40900-023-00440-7 |
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