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Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network

BACKGROUND: The Chronic Pain Network (CPN) is a pan-Canadian research network focused on innovating and improving the quality and delivery of pain prevention, assessment, management and research for all Canadians. An important focus of the CPN is to work in collaboration with patient partners. Patie...

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Autores principales: Tripp, Laura, Richards, Dawn P., Daly-Cyr, Jennifer, Lane, Therese, Linkiewich, Delane, Begley, Kimberly N., Buckley, Norman, Hudspith, Maria, Poulin, Patricia, Abelson, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466858/
https://www.ncbi.nlm.nih.gov/pubmed/37649098
http://dx.doi.org/10.1186/s40900-023-00491-w
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author Tripp, Laura
Richards, Dawn P.
Daly-Cyr, Jennifer
Lane, Therese
Linkiewich, Delane
Begley, Kimberly N.
Buckley, Norman
Hudspith, Maria
Poulin, Patricia
Abelson, Julia
author_facet Tripp, Laura
Richards, Dawn P.
Daly-Cyr, Jennifer
Lane, Therese
Linkiewich, Delane
Begley, Kimberly N.
Buckley, Norman
Hudspith, Maria
Poulin, Patricia
Abelson, Julia
author_sort Tripp, Laura
collection PubMed
description BACKGROUND: The Chronic Pain Network (CPN) is a pan-Canadian research network focused on innovating and improving the quality and delivery of pain prevention, assessment, management and research for all Canadians. An important focus of the CPN is to work in collaboration with patient partners. Patient partners, researchers and clinicians work together in all aspects of the research network including on funded research projects and in the governance of the Network. Given this focus, the CPN identified the importance of evaluating their patient engagement work to understand its functioning and impact. METHODS: The objective of this exploratory evaluation case study was to understand the impacts of patient engagement on the CPN. The CPN worked with an external evaluation team which established an arms-length approach to the evaluation. Interviews were conducted with CPN members, including patient partners, leadership, funded researchers and committee co-chairs, at three discrete time points to trace the evolution of the patient engagement program within the Network. Key Network documents were also collected and reviewed. Data were analyzed following each set of interviews using content analysis guided by the principles of constant comparison and qualitative description. A final round of analysis was conducted using the Engage with Impact Toolkit, an impact measurement framework, to identify impacts of engagement. RESULTS: Impacts of patient engagement were identified at the individual, network, funded research project and research community levels. These impacts were observed in the following areas: (1) building community; (2) developing knowledge, skills and resources; (3) increasing confidence; (4) influencing priorities and decisions; (5) enabling additional opportunities; (6) promoting culture change; and, (7) coping with experiences of living with chronic pain. CONCLUSIONS: While not without challenges, the patient engagement efforts of the CPN demonstrates the impact engaging patient partners can have on a national research network and related policy activities. Understanding the approaches to, and impacts of, patient engagement on health research networks can illuminate the value of having patient partners engaged in all aspects of a research network and should serve as encouragement to others who look to take on similar work. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40900-023-00491-w.
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spelling pubmed-104668582023-08-31 Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network Tripp, Laura Richards, Dawn P. Daly-Cyr, Jennifer Lane, Therese Linkiewich, Delane Begley, Kimberly N. Buckley, Norman Hudspith, Maria Poulin, Patricia Abelson, Julia Res Involv Engagem Research BACKGROUND: The Chronic Pain Network (CPN) is a pan-Canadian research network focused on innovating and improving the quality and delivery of pain prevention, assessment, management and research for all Canadians. An important focus of the CPN is to work in collaboration with patient partners. Patient partners, researchers and clinicians work together in all aspects of the research network including on funded research projects and in the governance of the Network. Given this focus, the CPN identified the importance of evaluating their patient engagement work to understand its functioning and impact. METHODS: The objective of this exploratory evaluation case study was to understand the impacts of patient engagement on the CPN. The CPN worked with an external evaluation team which established an arms-length approach to the evaluation. Interviews were conducted with CPN members, including patient partners, leadership, funded researchers and committee co-chairs, at three discrete time points to trace the evolution of the patient engagement program within the Network. Key Network documents were also collected and reviewed. Data were analyzed following each set of interviews using content analysis guided by the principles of constant comparison and qualitative description. A final round of analysis was conducted using the Engage with Impact Toolkit, an impact measurement framework, to identify impacts of engagement. RESULTS: Impacts of patient engagement were identified at the individual, network, funded research project and research community levels. These impacts were observed in the following areas: (1) building community; (2) developing knowledge, skills and resources; (3) increasing confidence; (4) influencing priorities and decisions; (5) enabling additional opportunities; (6) promoting culture change; and, (7) coping with experiences of living with chronic pain. CONCLUSIONS: While not without challenges, the patient engagement efforts of the CPN demonstrates the impact engaging patient partners can have on a national research network and related policy activities. Understanding the approaches to, and impacts of, patient engagement on health research networks can illuminate the value of having patient partners engaged in all aspects of a research network and should serve as encouragement to others who look to take on similar work. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40900-023-00491-w. BioMed Central 2023-08-30 /pmc/articles/PMC10466858/ /pubmed/37649098 http://dx.doi.org/10.1186/s40900-023-00491-w 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 Research
Tripp, Laura
Richards, Dawn P.
Daly-Cyr, Jennifer
Lane, Therese
Linkiewich, Delane
Begley, Kimberly N.
Buckley, Norman
Hudspith, Maria
Poulin, Patricia
Abelson, Julia
Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title_full Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title_fullStr Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title_full_unstemmed Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title_short Evaluating the impacts of patient engagement on a national health research network: results of a case study of the Chronic Pain Network
title_sort evaluating the impacts of patient engagement on a national health research network: results of a case study of the chronic pain network
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466858/
https://www.ncbi.nlm.nih.gov/pubmed/37649098
http://dx.doi.org/10.1186/s40900-023-00491-w
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