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Exploring the outcomes of research engagement using the observation method in an online setting.
Marshall, Deborah A; Suryaprakash, Nitya; Lavallee, Danielle C; Barker, Karis L; Mackean, Gail; Zelinsky, Sandra; McCarron, Tamara L; Santana, Maria J; Moayyedi, Paul; Bryan, Stirling.
Afiliación
  • Marshall DA; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada damarsha@ucalgary.ca.
  • Suryaprakash N; IMAGINE SPOR Chronic Disease Network, Hamilton, Ontario, Canada.
  • Lavallee DC; The University of British Columbia School of Population and Public Health, Vancouver, British Columbia, Canada.
  • Barker KL; The University of British Columbia School of Population and Public Health, Vancouver, British Columbia, Canada.
  • Mackean G; Michael Smith Health Research, Vancouver, British Columbia, Canada.
  • Zelinsky S; British Columbia SPOR SUPPORT Unit, Vancouver, British Columbia, Canada.
  • McCarron TL; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Santana MJ; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Moayyedi P; Department of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
  • Bryan S; IMAGINE SPOR Chronic Disease Network, Hamilton, Ontario, Canada.
BMJ Open ; 13(11): e073953, 2023 11 21.
Article en En | MEDLINE | ID: mdl-37989365
OBJECTIVE: The objective of this study was to explore the outcomes of research engagement (patient engagement, PE) in the context of qualitative research. DESIGN: We observed engagement in two groups comprised of patients, clinicians and researchers tasked with conducting a qualitative preference exploration project in inflammatory bowel disease. One group was led by a patient research partner (PLG, partner led group) and the other by an academic researcher (RLG, researcher led group). A semistructured guide and a set of critical outcomes of research engagement were used as a framework to ground our analysis. SETTING: The study was conducted online. PARTICIPANTS: Patient research partners (n=5), researchers (n=5) and clinicians (n=4) participated in this study. MAIN OUTCOME MEASURES: Transcripts of meetings, descriptive and reflective observation data of engagement during meetings and email correspondence between group members were analysed to identify the outcomes of PE. RESULTS: Both projects were patient-centred, collaborative, meaningful, rigorous, adaptable, ethical, legitimate, understandable, feasible, timely and sustainable. Patient research partners (PRPs) in both groups wore dual hats as patients and researchers and influenced project decisions wearing both hats. They took on advisory and operational roles. Collaboration seemed easier in the PLG than in the RLG. The RLG PRPs spent more time than their counterparts in the PLG sharing their experience with biologics and helping their group identify a meaningful project question. A formal literature review informed the design, project materials and analysis in the RLG, while the formal review informed the project materials and analysis in the PLG. A PRP in the RLG and the PLG lead leveraged personal connections to facilitate recruitment. The outcomes of both projects were meaningful to all members of the groups. CONCLUSIONS: Our findings show that engagement of PRPs in research has a positive influence on the project design and delivery in the context of qualitative research in both the patient-led and researcher-led group.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Productos Biológicos / Enfermedades Inflamatorias del Intestino Límite: Humans Idioma: En Revista: BMJ Open Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Productos Biológicos / Enfermedades Inflamatorias del Intestino Límite: Humans Idioma: En Revista: BMJ Open Año: 2023 Tipo del documento: Article País de afiliación: Canadá
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