患者合作伙伴的观点:参与共同设计的虚拟现实项目的体验。

IF 1.6 Q3 HEALTH CARE SCIENCES & SERVICES Journal of Patient Experience Pub Date : 2024-12-12 eCollection Date: 2024-01-01 DOI:10.1177/23743735241302932
Heather Thomson, Lisa Di Prospero, Sarah Xiao, Tamara Harth, Laurie Legere, Laura Rashleigh, Maria Parzanese
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引用次数: 0

摘要

患者伴侣(PP)可以通过他们的生活经历和个人叙述为医疗保健做出有意义的贡献。然而,研究人员必须确保患者在知识生成过程中真实地和协作地参与进来。作为一个更大项目的一部分,4名PP参与了一个虚拟现实视频的共同设计,旨在促进对COVID-19大流行初期患者生活经历的理解。本文报告了对PP参与该项目的经验的后续评估访谈的结果。访谈记录的专题分析得出了两个主要主题,以及PP参与的促进因素和障碍。参与该项目的主要原因是为社区做出贡献和回馈,为受COVID-19影响的患者带来改变。参与为PP带来了积极的体验和影响。参与的促进因素包括感觉被倾听、被重视和被尊重。障碍包括完成项目所需的时间长度以及PP的健康状况。
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Patient Partner Perspectives: The Experience of Participating in a Co-Designed Virtual Reality Project.

Patient partners (PP) are well positioned to make meaningful contributions to healthcare through their lived experiences and personal narratives. However, researchers must ensure that patients are engaged authentically and collaboratively in knowledge generation. As part of a larger project, 4 PP were engaged in the co-design of a virtual reality video aimed at promoting an understanding of patients' lived experience with COVID-19 during the initial phase of the pandemic. This paper reports on findings from follow-up evaluation interviews with PP about their experiences participating in this project. Thematic analysis of interview transcripts resulted in 2 major themes as well as facilitators and barriers to PP engagement. Primary reasons to participate in the project were to contribute and give back to the community and make a difference for patients impacted by COVID-19. Engagement resulted in positive experiences and impacts for PP. Facilitators to engagement included feeling heard, being valued, and treated with respect. Barriers included length of time required to complete the project as well as PP health status.

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来源期刊
Journal of Patient Experience
Journal of Patient Experience HEALTH CARE SCIENCES & SERVICES-
CiteScore
2.00
自引率
6.70%
发文量
178
审稿时长
15 weeks
期刊最新文献
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