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What motivates public collaborators to become and stay involved in health research?
People with lived experience of health and illness are increasingly being involved in research. Knowing what creates interest in becoming involved in health research may help identify appropriate ways of facilitating meaningful involvement. The study aimed to investigate why people became public col...
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Published in: | Research involvement and engagement 2024-02, Vol.10 (1), p.24-24, Article 24 |
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creator | Røssvoll, Toril Beate Liabo, Kristin Hanssen, Tove Aminda Rosenvinge, Jan H Sundkvist, Elisabeth Pettersen, Gunn |
description | People with lived experience of health and illness are increasingly being involved in research. Knowing what creates interest in becoming involved in health research may help identify appropriate ways of facilitating meaningful involvement. The study aimed to investigate why people became public collaborators in health research and what helped sustain their commitment to staying involved.
Semistructured individual qualitative interviews were conducted with 11 Norwegian public collaborators recruited from patient organisations. To enhance the quality and relevance of this study, three public collaborators were involved in framing the study and in the data analysis. One of them is a coauthor of this paper. The interviews were analysed through reflexive thematic analysis, and two themes were generated.
The first theme, 'research as a vehicle to impact' showed how interest in becoming involved in research was founded on the possibility of impacting healthcare through research. Other inspiring factors were how they appraised the relevance of the research, in addition to the public collaborators' own sense of moral duty to advocate for research related to their own as well as others, illnesses or diseases. The second theme, ''Acknowledgement and accessibility', framed how the participants perceived appreciation of experiential knowledge as crucial for maintaining motivation in their role as public collaborators. Other promoters of sustained involvement presented were training for both public collaborators and researchers, adequate allowance as a means for visualising and valuing PPI, and accessible language.
This study contributes to the understanding of how to facilitate meaningful and sustainable PPI, which requires a safe space for collaboration and attention to accessibility. Facilitating meaningful involvement may, in turn, increase the potential impact and sustainability of PPI. |
doi_str_mv | 10.1186/s40900-024-00555-5 |
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Semistructured individual qualitative interviews were conducted with 11 Norwegian public collaborators recruited from patient organisations. To enhance the quality and relevance of this study, three public collaborators were involved in framing the study and in the data analysis. One of them is a coauthor of this paper. The interviews were analysed through reflexive thematic analysis, and two themes were generated.
The first theme, 'research as a vehicle to impact' showed how interest in becoming involved in research was founded on the possibility of impacting healthcare through research. Other inspiring factors were how they appraised the relevance of the research, in addition to the public collaborators' own sense of moral duty to advocate for research related to their own as well as others, illnesses or diseases. The second theme, ''Acknowledgement and accessibility', framed how the participants perceived appreciation of experiential knowledge as crucial for maintaining motivation in their role as public collaborators. Other promoters of sustained involvement presented were training for both public collaborators and researchers, adequate allowance as a means for visualising and valuing PPI, and accessible language.
This study contributes to the understanding of how to facilitate meaningful and sustainable PPI, which requires a safe space for collaboration and attention to accessibility. Facilitating meaningful involvement may, in turn, increase the potential impact and sustainability of PPI.</description><identifier>ISSN: 2056-7529</identifier><identifier>EISSN: 2056-7529</identifier><identifier>DOI: 10.1186/s40900-024-00555-5</identifier><identifier>PMID: 38347609</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Chronic illnesses ; Collaboration ; Data analysis ; Information management ; Interviews ; Knowledge ; Maintaining motivation ; Medical research ; Medicine, Experimental ; Patient and public involvement ; Patient satisfaction ; Patients ; People with disabilities ; Public collaborator ; Public health ; Qualitative research ; Reflexive thematic analysis ; Researchers ; Sustainability ; Teams</subject><ispartof>Research involvement and engagement, 2024-02, Vol.10 (1), p.24-24, Article 24</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4645-453ead870020db579a5d8d365e2501e50f829b24e9c80450afa91f663b91fd643</cites><orcidid>0000-0003-2797-3497</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10863223/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2925667688?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38347609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Røssvoll, Toril Beate</creatorcontrib><creatorcontrib>Liabo, Kristin</creatorcontrib><creatorcontrib>Hanssen, Tove Aminda</creatorcontrib><creatorcontrib>Rosenvinge, Jan H</creatorcontrib><creatorcontrib>Sundkvist, Elisabeth</creatorcontrib><creatorcontrib>Pettersen, Gunn</creatorcontrib><title>What motivates public collaborators to become and stay involved in health research?</title><title>Research involvement and engagement</title><addtitle>Res Involv Engagem</addtitle><description>People with lived experience of health and illness are increasingly being involved in research. Knowing what creates interest in becoming involved in health research may help identify appropriate ways of facilitating meaningful involvement. The study aimed to investigate why people became public collaborators in health research and what helped sustain their commitment to staying involved.
Semistructured individual qualitative interviews were conducted with 11 Norwegian public collaborators recruited from patient organisations. To enhance the quality and relevance of this study, three public collaborators were involved in framing the study and in the data analysis. One of them is a coauthor of this paper. The interviews were analysed through reflexive thematic analysis, and two themes were generated.
The first theme, 'research as a vehicle to impact' showed how interest in becoming involved in research was founded on the possibility of impacting healthcare through research. Other inspiring factors were how they appraised the relevance of the research, in addition to the public collaborators' own sense of moral duty to advocate for research related to their own as well as others, illnesses or diseases. The second theme, ''Acknowledgement and accessibility', framed how the participants perceived appreciation of experiential knowledge as crucial for maintaining motivation in their role as public collaborators. Other promoters of sustained involvement presented were training for both public collaborators and researchers, adequate allowance as a means for visualising and valuing PPI, and accessible language.
This study contributes to the understanding of how to facilitate meaningful and sustainable PPI, which requires a safe space for collaboration and attention to accessibility. Facilitating meaningful involvement may, in turn, increase the potential impact and sustainability of PPI.</description><subject>Chronic illnesses</subject><subject>Collaboration</subject><subject>Data analysis</subject><subject>Information management</subject><subject>Interviews</subject><subject>Knowledge</subject><subject>Maintaining motivation</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Patient and public involvement</subject><subject>Patient satisfaction</subject><subject>Patients</subject><subject>People with disabilities</subject><subject>Public collaborator</subject><subject>Public health</subject><subject>Qualitative research</subject><subject>Reflexive thematic analysis</subject><subject>Researchers</subject><subject>Sustainability</subject><subject>Teams</subject><issn>2056-7529</issn><issn>2056-7529</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptks1q3DAUhU1paUKaF-iiGLppF06v9Wd5FULoz0Cg0LR0Ka7l6xkNtpVKmiF5-2oyaZopxQsJ-buf0OEUxesazupaqw9RQAtQARMVgJSyks-KYwZSVY1k7fMn-6PiNMY1ANSNlNDql8UR11w0Ctrj4vrnClM5-eS2mCiWN5tudLa0fhyx8wGTD7FMvuzI-olKnPsyJrwr3bz145b6vClXhGNalYEiYbCr81fFiwHHSKcP60nx49PH75dfqquvnxeXF1eVFUrISkhO2OsGgEHfyaZF2eueK0lMQk0SBs3ajglqrQYhAQds60Ep3uWlV4KfFIu9t_e4NjfBTRjujEdn7g98WBoMydmRDDSy46LDQehadIqQSyI1DCBrln0yu873rhzARL2lOQUcD6SHf2a3Mku_NTVoxRnj2fDuwRD8rw3FZCYXLeUcZ_KbaFjLFDT5SZDRt_-ga78Jc85qR0mlGqX1X2qJ-QVuHny-2O6k5iJ7mNJM7Kiz_1D562ly1s80uHx-MPD-YCAziW7TEjcxmsX1t0OW7VkbfIyBhsdAajC7Gpp9DU2uobmvodlF-eZplI8jf0rHfwNq_9Tc</recordid><startdate>20240212</startdate><enddate>20240212</enddate><creator>Røssvoll, Toril Beate</creator><creator>Liabo, Kristin</creator><creator>Hanssen, Tove Aminda</creator><creator>Rosenvinge, Jan H</creator><creator>Sundkvist, Elisabeth</creator><creator>Pettersen, Gunn</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2797-3497</orcidid></search><sort><creationdate>20240212</creationdate><title>What motivates public collaborators to become and stay involved in health research?</title><author>Røssvoll, Toril Beate ; Liabo, Kristin ; Hanssen, Tove Aminda ; Rosenvinge, Jan H ; Sundkvist, Elisabeth ; Pettersen, Gunn</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4645-453ead870020db579a5d8d365e2501e50f829b24e9c80450afa91f663b91fd643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Chronic illnesses</topic><topic>Collaboration</topic><topic>Data analysis</topic><topic>Information management</topic><topic>Interviews</topic><topic>Knowledge</topic><topic>Maintaining motivation</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Patient and public involvement</topic><topic>Patient satisfaction</topic><topic>Patients</topic><topic>People with disabilities</topic><topic>Public collaborator</topic><topic>Public health</topic><topic>Qualitative research</topic><topic>Reflexive thematic analysis</topic><topic>Researchers</topic><topic>Sustainability</topic><topic>Teams</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Røssvoll, Toril Beate</creatorcontrib><creatorcontrib>Liabo, Kristin</creatorcontrib><creatorcontrib>Hanssen, Tove Aminda</creatorcontrib><creatorcontrib>Rosenvinge, Jan H</creatorcontrib><creatorcontrib>Sundkvist, Elisabeth</creatorcontrib><creatorcontrib>Pettersen, Gunn</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Research involvement and engagement</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Røssvoll, Toril Beate</au><au>Liabo, Kristin</au><au>Hanssen, Tove Aminda</au><au>Rosenvinge, Jan H</au><au>Sundkvist, Elisabeth</au><au>Pettersen, Gunn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>What motivates public collaborators to become and stay involved in health research?</atitle><jtitle>Research involvement and engagement</jtitle><addtitle>Res Involv Engagem</addtitle><date>2024-02-12</date><risdate>2024</risdate><volume>10</volume><issue>1</issue><spage>24</spage><epage>24</epage><pages>24-24</pages><artnum>24</artnum><issn>2056-7529</issn><eissn>2056-7529</eissn><abstract>People with lived experience of health and illness are increasingly being involved in research. Knowing what creates interest in becoming involved in health research may help identify appropriate ways of facilitating meaningful involvement. The study aimed to investigate why people became public collaborators in health research and what helped sustain their commitment to staying involved.
Semistructured individual qualitative interviews were conducted with 11 Norwegian public collaborators recruited from patient organisations. To enhance the quality and relevance of this study, three public collaborators were involved in framing the study and in the data analysis. One of them is a coauthor of this paper. The interviews were analysed through reflexive thematic analysis, and two themes were generated.
The first theme, 'research as a vehicle to impact' showed how interest in becoming involved in research was founded on the possibility of impacting healthcare through research. Other inspiring factors were how they appraised the relevance of the research, in addition to the public collaborators' own sense of moral duty to advocate for research related to their own as well as others, illnesses or diseases. The second theme, ''Acknowledgement and accessibility', framed how the participants perceived appreciation of experiential knowledge as crucial for maintaining motivation in their role as public collaborators. Other promoters of sustained involvement presented were training for both public collaborators and researchers, adequate allowance as a means for visualising and valuing PPI, and accessible language.
This study contributes to the understanding of how to facilitate meaningful and sustainable PPI, which requires a safe space for collaboration and attention to accessibility. Facilitating meaningful involvement may, in turn, increase the potential impact and sustainability of PPI.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38347609</pmid><doi>10.1186/s40900-024-00555-5</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2797-3497</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Chronic illnesses Collaboration Data analysis Information management Interviews Knowledge Maintaining motivation Medical research Medicine, Experimental Patient and public involvement Patient satisfaction Patients People with disabilities Public collaborator Public health Qualitative research Reflexive thematic analysis Researchers Sustainability Teams |
title | What motivates public collaborators to become and stay involved in health research? |
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