让性与性别少数群体 (SGM) 社区参与健康研究:建立和维持 PRIDEnet

J. Obedin-Maliver, Carolyn Hunt, A. Flentje, Cassie Armea-Warren, Mahri Bahati, M. Lubensky, Zubin Dastur, Chloe Eastburn, Ell Hundertmark, Daniel Moretti, Anthony Pho, Ana Rescate, Richard E. Greene, Philip-Jamal Thomas Williams, Devin Hursey, Loree Cooke Daniels, M. Lunn
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引用次数: 0

摘要

女同性恋、男同性恋、双性恋、变性人、同性恋者、双性人、无性恋者、芳香恋者以及其他性少数群体和/或性别少数群体(LGBTQIA+)群体在健康研究中的代表性不足,并存在有据可查的健康差异。此外,LGBTQIA+ 群体在医疗保健和健康研究环境中还遭受过虐待、歧视和侮辱。让 LGBTQIA+ 群体和个人有效参与健康研究对于开发具有代表性的数据集、改善医疗保健服务和政策以及减少差异至关重要。然而,人们对哪些参与方式对 LGBTQIA+ 群体有效却知之甚少。本文介绍了 PRIDEnet (pridenet.org)的发展情况,这是一个致力于促进 LGBTQIA+ 社区参与健康研究的全国性网络,它建立在成熟的社区参与研究 (CEnR) 原则之上。PRIDEnet 的关系建设和数字通信活动吸引了全国数以千计的 LGBTQIA+ 认同者参与,并提供了多种低门槛的方式来参与特定研究和影响研究。这些活动构成了一个 CEnR 基础设施,代表其他项目(主要是 PRIDE 研究 (pridestudy.org) 和美国国立卫生研究院的 "我们所有人 "研究计划 (joinallofus.org/lgbtqia))吸引 LGBTQIA+ 参与。我们的影响、成果和经验教训适用于那些让得不到充分服务的社区参与生物医学研究的人,其中包括:建立可长期维持变革关系的适应性基础设施的重要性;开展高接触活动以建立信任,开展广接触活动以建立大型数据集;培养一支由不同专业人士组成的团队,他们的生活经历反映了要参与研究的社区的生活经历;以及保持 CEnR 机制,使其超越提供建议的范围,自始至终为研究做出实质性贡献。
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Engaging Sexual and Gender Minority (SGM) Communities for Health Research: Building and Sustaining PRIDEnet
Lesbian, gay, bisexual, transgender, queer, intersex, asexual, aromantic, and other sexual and/or gender minority (LGBTQIA+) communities are underrepresented in health research and subject to documented health disparities. In addition, LGBTQIA+ communities have experienced mistreatment, discrimination, and stigma in health care and health research settings. Effectively engaging LGBTQIA+ communities and individuals in health research is critical to developing representative data sets, improving health care provision and policy, and reducing disparities. However, little is known about what engagement approaches work well with LGBTQIA+ people. This paper describes the development of PRIDEnet (pridenet.org), a national network dedicated to catalyzing LGBTQIA+ community involvement in health research and built upon well-established community-engaged research (CEnR) principles. PRIDEnet’s relationship building and digital communications activities engage thousands of LGBTQIA+-identified people across the country and offer multiple low-threshold ways to participate in specific studies and shape research. These activities comprise a CEnR infrastructure that engages LGBTQIA+ people on behalf of other projects, primarily The PRIDE Study (pridestudy.org) and the National Institutes of Health’s All of Us Research Program (joinallofus.org/lgbtqia). Our impact, results, and lessons learned apply to those engaging communities underserved in biomedical research and include: the importance of building adaptable infrastructure that sustains transformational relationships long-term; implementing high-touch activities to establish trust and broad-reach activities to build large data sets; nurturing a team of diverse professionals with lived experiences that reflect those of the communities to be engaged; and maintaining CEnR mechanisms that exceed advice-giving and result in substantive research contributions from beginning to end.
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