An empirically based conceptual framework for fostering meaningful patient engagement in research

Background Patient engagement in research (PEIR) is promoted to improve the relevance and quality of health research, but has little conceptualization derived from empirical data. Objective To address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR foun...

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Veröffentlicht in:Health expectations : an international journal of public participation in health care and health policy 2018-02, Vol.21 (1), p.396-406
Hauptverfasser: Hamilton, Clayon B., Hoens, Alison M., Backman, Catherine L., McKinnon, Annette M., McQuitty, Shanon, English, Kelly, Li, Linda C.
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container_issue 1
container_start_page 396
container_title Health expectations : an international journal of public participation in health care and health policy
container_volume 21
creator Hamilton, Clayon B.
Hoens, Alison M.
Backman, Catherine L.
McKinnon, Annette M.
McQuitty, Shanon
English, Kelly
Li, Linda C.
description Background Patient engagement in research (PEIR) is promoted to improve the relevance and quality of health research, but has little conceptualization derived from empirical data. Objective To address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR founded on a patient perspective. Methods We conducted a qualitative secondary analysis of in‐depth interviews with 18 patient research partners from a research centre‐affiliated patient advisory board. Data analysis involved three phases: identifying the themes, developing a framework and confirming the framework. We coded and organized the data, and ed, illustrated, described and explored the emergent themes using thematic analysis. Directed content analysis was conducted to derive concepts from 18 publications related to PEIR to supplement, confirm or refute, and extend the emergent conceptual framework. The framework was reviewed by four patient research partners on our research team. Results Participants’ experiences of working with researchers were generally positive. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. This framework, the PEIR Framework, was endorsed by the patient research partners on our team. Conclusions The PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR. It could be particularly useful when patient‐researcher partnerships are led by researchers with little experience of engaging patients in research.
doi_str_mv 10.1111/hex.12635
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Objective To address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR founded on a patient perspective. Methods We conducted a qualitative secondary analysis of in‐depth interviews with 18 patient research partners from a research centre‐affiliated patient advisory board. Data analysis involved three phases: identifying the themes, developing a framework and confirming the framework. We coded and organized the data, and ed, illustrated, described and explored the emergent themes using thematic analysis. Directed content analysis was conducted to derive concepts from 18 publications related to PEIR to supplement, confirm or refute, and extend the emergent conceptual framework. The framework was reviewed by four patient research partners on our research team. Results Participants’ experiences of working with researchers were generally positive. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. This framework, the PEIR Framework, was endorsed by the patient research partners on our team. Conclusions The PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR. It could be particularly useful when patient‐researcher partnerships are led by researchers with little experience of engaging patients in research.</description><identifier>ISSN: 1369-6513</identifier><identifier>EISSN: 1369-7625</identifier><identifier>DOI: 10.1111/hex.12635</identifier><identifier>PMID: 28984405</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Analysis ; Arthritis ; Caregivers ; Collaboration ; Community Participation ; Concepts ; conceptual framework ; Content analysis ; Data analysis ; Demography ; Education ; Empirical analysis ; Empowerment ; Female ; Health status ; Humans ; Information management ; Interviews ; Interviews as Topic ; Knowledge ; Male ; Medical research ; Medicine, Experimental ; Middle Aged ; Original Research Paper ; Original Research Papers ; Participation ; Partnerships ; patient and public involvement ; patient engagement in research ; Patient Participation ; Patients ; patient‐oriented research ; Qualitative analysis ; Qualitative Research ; Research Design ; Research Personnel ; Researchers ; Secondary analysis ; Teams ; Working groups</subject><ispartof>Health expectations : an international journal of public participation in health care and health policy, 2018-02, Vol.21 (1), p.396-406</ispartof><rights>2017 The Authors Health Expectations Published by John Wiley &amp; Sons Ltd</rights><rights>2017 The Authors Health Expectations Published by John Wiley &amp; Sons Ltd.</rights><rights>COPYRIGHT 2017 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2018 John Wiley &amp; Sons Ltd</rights><rights>2018. 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Objective To address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR founded on a patient perspective. Methods We conducted a qualitative secondary analysis of in‐depth interviews with 18 patient research partners from a research centre‐affiliated patient advisory board. Data analysis involved three phases: identifying the themes, developing a framework and confirming the framework. We coded and organized the data, and ed, illustrated, described and explored the emergent themes using thematic analysis. Directed content analysis was conducted to derive concepts from 18 publications related to PEIR to supplement, confirm or refute, and extend the emergent conceptual framework. The framework was reviewed by four patient research partners on our research team. Results Participants’ experiences of working with researchers were generally positive. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. This framework, the PEIR Framework, was endorsed by the patient research partners on our team. Conclusions The PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR. 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Objective To address this issue, we sought to develop an empirically based conceptual framework for meaningful PEIR founded on a patient perspective. Methods We conducted a qualitative secondary analysis of in‐depth interviews with 18 patient research partners from a research centre‐affiliated patient advisory board. Data analysis involved three phases: identifying the themes, developing a framework and confirming the framework. We coded and organized the data, and ed, illustrated, described and explored the emergent themes using thematic analysis. Directed content analysis was conducted to derive concepts from 18 publications related to PEIR to supplement, confirm or refute, and extend the emergent conceptual framework. The framework was reviewed by four patient research partners on our research team. Results Participants’ experiences of working with researchers were generally positive. Eight themes emerged: procedural requirements, convenience, contributions, support, team interaction, research environment, feel valued and benefits. These themes were interconnected and formed a conceptual framework to explain the phenomenon of meaningful PEIR from a patient perspective. This framework, the PEIR Framework, was endorsed by the patient research partners on our team. Conclusions The PEIR Framework provides guidance on aspects of PEIR to address for meaningful PEIR. It could be particularly useful when patient‐researcher partnerships are led by researchers with little experience of engaging patients in research.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>28984405</pmid><doi>10.1111/hex.12635</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-6852-3436</orcidid><oa>free_for_read</oa></addata></record>
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subjects Analysis
Arthritis
Caregivers
Collaboration
Community Participation
Concepts
conceptual framework
Content analysis
Data analysis
Demography
Education
Empirical analysis
Empowerment
Female
Health status
Humans
Information management
Interviews
Interviews as Topic
Knowledge
Male
Medical research
Medicine, Experimental
Middle Aged
Original Research Paper
Original Research Papers
Participation
Partnerships
patient and public involvement
patient engagement in research
Patient Participation
Patients
patient‐oriented research
Qualitative analysis
Qualitative Research
Research Design
Research Personnel
Researchers
Secondary analysis
Teams
Working groups
title An empirically based conceptual framework for fostering meaningful patient engagement in research
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