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Developing a Canadian evaluation framework for patient and public engagement in research: study protocol
BACKGROUND: Patient and public engagement (PPE) in research is growing internationally, and with it, the interest for its evaluation. In Canada, the Strategy for Patient-Oriented Research has generated national momentum and opportunities for greater PPE in research and health-system transformation....
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905422/ https://www.ncbi.nlm.nih.gov/pubmed/33632329 http://dx.doi.org/10.1186/s40900-021-00255-4 |
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author | L’Espérance, Audrey O’Brien, Nadia Grégoire, Alexandre Abelson, Julia Canfield, Carolyn Del Grande, Claudio Dogba, Maman Joyce Fancott, Carol Levasseur, Mary Anne Loignon, Christine Majnemer, Annette Pomey, Marie-Pascale Rasiah, Jananee Salsberg, Jon Santana, Maria Tremblay, Marie-Claude Urquhart, Robin Boivin, Antoine |
author_facet | L’Espérance, Audrey O’Brien, Nadia Grégoire, Alexandre Abelson, Julia Canfield, Carolyn Del Grande, Claudio Dogba, Maman Joyce Fancott, Carol Levasseur, Mary Anne Loignon, Christine Majnemer, Annette Pomey, Marie-Pascale Rasiah, Jananee Salsberg, Jon Santana, Maria Tremblay, Marie-Claude Urquhart, Robin Boivin, Antoine |
author_sort | L’Espérance, Audrey |
collection | PubMed |
description | BACKGROUND: Patient and public engagement (PPE) in research is growing internationally, and with it, the interest for its evaluation. In Canada, the Strategy for Patient-Oriented Research has generated national momentum and opportunities for greater PPE in research and health-system transformation. As is the case with most countries, the Canadian research community lacks a common evaluation framework for PPE, thus limiting our capacity to ensure integrity between principles and practices, learn across projects, identify common areas for improvement, and assess the impacts of engagement. OBJECTIVE: 1. Building consensus on common evaluation criteria and indicators for PPE in research; 2. Defining recommendations to implement and adapt the framework to specific populations. METHODS: Using a collaborative action-research approach, a national coalition of patient-oriented research leaders, (patient and community partners, engagement practitioners, researchers and health system leaders) will co-design the evaluation framework. We will develop core evaluation domains of the logic model by conducting a series of virtual consensus meetings using a nominal group technique with 50 patient partners and engagement practitioners, identified through 18 national research organizations. We will then conduct two Delphi rounds to prioritize process and impact indicators with 200 participants purposely recruited to include respondents from seldom-heard groups. Six expert working groups will define recommendations to implement and adapt the framework to research with specific populations, including Indigenous communities, immigrants, people with intellectual and physical disabilities, caregivers, and people with low literacy. Each step of framework development will be guided by an equity, diversity and inclusion approach in an effort to ensure that the participants engaged, the content produced, and the adaptation strategies proposed are relevant to diverse PPE. DISCUSSION: The potential contributions of this project are threefold: 1) support a national learning environment for engagement by offering a common blueprint for collaborative evaluation to the Canadian research community; 2) inform the international research community on potential (virtual) methodologies to build national consensus on common engagement evaluation frameworks; and 3) illustrate a shared attempt to engage patients and researchers in a strategic national initiative to strengthen evaluation capacity for PPE. |
format | Online Article Text |
id | pubmed-7905422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79054222021-02-25 Developing a Canadian evaluation framework for patient and public engagement in research: study protocol L’Espérance, Audrey O’Brien, Nadia Grégoire, Alexandre Abelson, Julia Canfield, Carolyn Del Grande, Claudio Dogba, Maman Joyce Fancott, Carol Levasseur, Mary Anne Loignon, Christine Majnemer, Annette Pomey, Marie-Pascale Rasiah, Jananee Salsberg, Jon Santana, Maria Tremblay, Marie-Claude Urquhart, Robin Boivin, Antoine Res Involv Engagem Protocol BACKGROUND: Patient and public engagement (PPE) in research is growing internationally, and with it, the interest for its evaluation. In Canada, the Strategy for Patient-Oriented Research has generated national momentum and opportunities for greater PPE in research and health-system transformation. As is the case with most countries, the Canadian research community lacks a common evaluation framework for PPE, thus limiting our capacity to ensure integrity between principles and practices, learn across projects, identify common areas for improvement, and assess the impacts of engagement. OBJECTIVE: 1. Building consensus on common evaluation criteria and indicators for PPE in research; 2. Defining recommendations to implement and adapt the framework to specific populations. METHODS: Using a collaborative action-research approach, a national coalition of patient-oriented research leaders, (patient and community partners, engagement practitioners, researchers and health system leaders) will co-design the evaluation framework. We will develop core evaluation domains of the logic model by conducting a series of virtual consensus meetings using a nominal group technique with 50 patient partners and engagement practitioners, identified through 18 national research organizations. We will then conduct two Delphi rounds to prioritize process and impact indicators with 200 participants purposely recruited to include respondents from seldom-heard groups. Six expert working groups will define recommendations to implement and adapt the framework to research with specific populations, including Indigenous communities, immigrants, people with intellectual and physical disabilities, caregivers, and people with low literacy. Each step of framework development will be guided by an equity, diversity and inclusion approach in an effort to ensure that the participants engaged, the content produced, and the adaptation strategies proposed are relevant to diverse PPE. DISCUSSION: The potential contributions of this project are threefold: 1) support a national learning environment for engagement by offering a common blueprint for collaborative evaluation to the Canadian research community; 2) inform the international research community on potential (virtual) methodologies to build national consensus on common engagement evaluation frameworks; and 3) illustrate a shared attempt to engage patients and researchers in a strategic national initiative to strengthen evaluation capacity for PPE. BioMed Central 2021-02-25 /pmc/articles/PMC7905422/ /pubmed/33632329 http://dx.doi.org/10.1186/s40900-021-00255-4 Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://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 L’Espérance, Audrey O’Brien, Nadia Grégoire, Alexandre Abelson, Julia Canfield, Carolyn Del Grande, Claudio Dogba, Maman Joyce Fancott, Carol Levasseur, Mary Anne Loignon, Christine Majnemer, Annette Pomey, Marie-Pascale Rasiah, Jananee Salsberg, Jon Santana, Maria Tremblay, Marie-Claude Urquhart, Robin Boivin, Antoine Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title | Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title_full | Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title_fullStr | Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title_full_unstemmed | Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title_short | Developing a Canadian evaluation framework for patient and public engagement in research: study protocol |
title_sort | developing a canadian evaluation framework for patient and public engagement in research: study protocol |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905422/ https://www.ncbi.nlm.nih.gov/pubmed/33632329 http://dx.doi.org/10.1186/s40900-021-00255-4 |
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