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Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year
BACKGROUND: The objective of this paper is to describe the activities, challenges and mitigation strategies, lessons learned and reflections on the importance of engagement from the first year of the Canadian Consortium on Neurodegeneration in Aging (CCNA) Engagement of People with Lived Experience...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233803/ https://www.ncbi.nlm.nih.gov/pubmed/35752841 http://dx.doi.org/10.1186/s40900-022-00359-5 |
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author | Snowball, Ellen Fernandez Loughlin, Rosette Eagleson, Heather Barnett, Karen Myers McLellan, Emily O’Connor, Denis Kelly, Catherine Thelker, Christine McGilton, Katherine S. Bethell, Jennifer |
author_facet | Snowball, Ellen Fernandez Loughlin, Rosette Eagleson, Heather Barnett, Karen Myers McLellan, Emily O’Connor, Denis Kelly, Catherine Thelker, Christine McGilton, Katherine S. Bethell, Jennifer |
author_sort | Snowball, Ellen |
collection | PubMed |
description | BACKGROUND: The objective of this paper is to describe the activities, challenges and mitigation strategies, lessons learned and reflections on the importance of engagement from the first year of the Canadian Consortium on Neurodegeneration in Aging (CCNA) Engagement of People with Lived Experience of Dementia (EPLED) Advisory Group and cross-cutting program. EPLED was created to support persons with dementia and care partners to be actively involved in the CCNA research process. MAIN BODY: The Advisory Group was formed to work with CCNA researchers and programs to develop new ways to further collaborate and advance the methods of patient engagement in research on dementia. A role profile and recruitment poster were developed and, after interviews, 17 people were invited to join the Advisory Group. We planned three online EPLED meetings to take place between July–August of 2020, with one in-person meeting to be held in Canada. Due to COVID-19, we moved all of these meetings online. In the first year, EPLED and the Advisory Group met seven times formally, four times informally, developed a website, engaged with CCNA research projects, participated in CCNA “Central” activities and formulated an evaluation plan. For researchers and people with lived experience of dementia, motivations for patient engagement included challenging stigma, making meaning from their experience (such as building relationships and having their voices heard) and contributing to research. Common challenges to engagement were related to navigating the impact of COVID-19, such as difficulty in getting to know each other and technical issues with video-conference software. We learned that developing trusting relationships, providing education, offering support, being flexible and acknowledging tensions between research, practice and lived experience, were vital to the success of the Advisory Group. CONCLUSION: The first year of the EPLED Advisory Group demonstrated the potential contributions of people with lived experience of dementia as partners in research. Building these collaborations with individuals and communities—people living with dementia, care partners, researchers and research institutions—has the potential for positive impact across these groups and, ultimately, improve the lives of people living with dementia and their care partners. |
format | Online Article Text |
id | pubmed-9233803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92338032022-06-27 Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year Snowball, Ellen Fernandez Loughlin, Rosette Eagleson, Heather Barnett, Karen Myers McLellan, Emily O’Connor, Denis Kelly, Catherine Thelker, Christine McGilton, Katherine S. Bethell, Jennifer Res Involv Engagem Commentary BACKGROUND: The objective of this paper is to describe the activities, challenges and mitigation strategies, lessons learned and reflections on the importance of engagement from the first year of the Canadian Consortium on Neurodegeneration in Aging (CCNA) Engagement of People with Lived Experience of Dementia (EPLED) Advisory Group and cross-cutting program. EPLED was created to support persons with dementia and care partners to be actively involved in the CCNA research process. MAIN BODY: The Advisory Group was formed to work with CCNA researchers and programs to develop new ways to further collaborate and advance the methods of patient engagement in research on dementia. A role profile and recruitment poster were developed and, after interviews, 17 people were invited to join the Advisory Group. We planned three online EPLED meetings to take place between July–August of 2020, with one in-person meeting to be held in Canada. Due to COVID-19, we moved all of these meetings online. In the first year, EPLED and the Advisory Group met seven times formally, four times informally, developed a website, engaged with CCNA research projects, participated in CCNA “Central” activities and formulated an evaluation plan. For researchers and people with lived experience of dementia, motivations for patient engagement included challenging stigma, making meaning from their experience (such as building relationships and having their voices heard) and contributing to research. Common challenges to engagement were related to navigating the impact of COVID-19, such as difficulty in getting to know each other and technical issues with video-conference software. We learned that developing trusting relationships, providing education, offering support, being flexible and acknowledging tensions between research, practice and lived experience, were vital to the success of the Advisory Group. CONCLUSION: The first year of the EPLED Advisory Group demonstrated the potential contributions of people with lived experience of dementia as partners in research. Building these collaborations with individuals and communities—people living with dementia, care partners, researchers and research institutions—has the potential for positive impact across these groups and, ultimately, improve the lives of people living with dementia and their care partners. BioMed Central 2022-06-25 /pmc/articles/PMC9233803/ /pubmed/35752841 http://dx.doi.org/10.1186/s40900-022-00359-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (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 | Commentary Snowball, Ellen Fernandez Loughlin, Rosette Eagleson, Heather Barnett, Karen Myers McLellan, Emily O’Connor, Denis Kelly, Catherine Thelker, Christine McGilton, Katherine S. Bethell, Jennifer Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title | Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title_full | Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title_fullStr | Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title_full_unstemmed | Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title_short | Engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
title_sort | engagement of people with lived experience of dementia advisory group and cross-cutting program: reflections on the first year |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233803/ https://www.ncbi.nlm.nih.gov/pubmed/35752841 http://dx.doi.org/10.1186/s40900-022-00359-5 |
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