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超越社区参与:荷兰艾滋病毒治愈研究中艾滋病毒感染者和受影响社区(MIPA)有意义参与的观点。

Beyond community engagement: perspectives on the meaningful involvement of people with HIV and affected communities (MIPA) in HIV cure research in The Netherlands.

机构信息

Department of Work and Social Psychology, Maastricht University, Maastricht, the Netherlands.

Department of Interdisciplinary Social Science, Utrecht University, Utrecht, The Netherlands.

出版信息

HIV Res Clin Pract. 2024 Dec;25(1):2335454. Epub 2024 Apr 5.

Abstract

BACKGROUND

Meaningful involvement of people with HIV and affected communities in HIV cure research is essential to ensuring that cure research efforts are conducted transparently, socially justly, and ethically. This study set out to investigate how people with HIV and affected communities are involved in cure research in the Netherlands and explore what can be done to optimize involvement and engagement.

METHODS

Eighty-five semi-structured online, telephone, and face-to-face interviews were conducted with people with HIV ( = 30), key populations ( = 35), and key informants (KI;  = 20) in the field of HIV. The interviews were analyzed using reflexive thematic analysis.

RESULTS

Awareness of the meaningful involvement of people with HIV (MIPA) efforts was low among people with HIV and key populations, which contrasted with KI, who exhibited greater awareness. People with HIV and KI emphasized the importance of MIPA in ensuring the representation of lived experiences in HIV cure research and fostering trust between communities and researchers. Practical implementations of MIPA were unclear, ultimately resulting in difficulties defining MIPA beyond clinical trial participation. People with HIV and key populations also doubted their skills and self-efficacy to make meaningful contributions when confronted with involvement beyond participating in research and clinical trials.

CONCLUSIONS

MIPA is crucial for improving the quality, transparency, and ethical conduct of HIV cure research. It emphasizes the need for increased awareness and funding, standardized guidelines to ensure meaningful involvement, and combat tokenism and misconceptions.

摘要

背景

让 HIV 感染者和受影响社区充分参与 HIV 治愈研究对于确保治愈研究工作透明、公正和符合伦理至关重要。本研究旨在调查荷兰 HIV 治愈研究中 HIV 感染者和受影响社区的参与情况,并探讨如何优化参与和投入。

方法

对 HIV 领域的 85 名 HIV 感染者( = 30)、重点人群( = 35)和关键信息提供者(KI; = 20)进行了 85 次在线、电话和面对面的半结构化访谈。使用反思性主题分析对访谈进行了分析。

结果

HIV 感染者和重点人群对 HIV 感染者有意义参与(MIPA)工作的认识程度较低,而 KI 对 MIPA 的认识程度较高。HIV 感染者和 KI 强调 MIPA 对于确保 HIV 治愈研究中体现真实经验以及在社区和研究人员之间建立信任的重要性。MIPA 的实际实施情况不明确,最终导致除了临床试验参与之外,很难定义 MIPA。HIV 感染者和重点人群在面临参与研究和临床试验以外的活动时,还对自己的技能和自我效能产生怀疑,认为自己无法做出有意义的贡献。

结论

MIPA 对于提高 HIV 治愈研究的质量、透明度和道德规范至关重要。它强调需要提高认识和资金投入,制定标准化指南以确保有意义的参与,并解决象征性参与和误解的问题。

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