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在全球卫生研究中共享权力:一个用于设计有意义地纳入社区的优先事项设定过程的伦理工具包。

Sharing power in global health research: an ethical toolkit for designing priority-setting processes that meaningfully include communities.

机构信息

Centre for Health Equity, School of Population and Global Health, University of Melbourne, 207 Bouverie St, Carlton, Victoria, 3053, Australia.

出版信息

Int J Equity Health. 2021 May 25;20(1):127. doi: 10.1186/s12939-021-01453-y.

Abstract

To promote social justice and equity, global health research should meaningfully engage communities throughout projects: from setting agendas onwards. But communities, especially those that are considered disadvantaged or marginalised, rarely have a say in the priorities of the research projects that aim to help them. So far, there remains limited ethical guidance and resources on how to share power with communities in health research priority-setting. This paper presents an "ethical toolkit" for academic researchers and their community partners to use to design priority-setting processes that meaningfully include the communities impacted by their projects. An empirical reflective equilibrium approach was employed to develop the toolkit. Conceptual work articulated ethical considerations related to sharing power in g0l0o0bal health research priority-setting, developed guidance on how to address them, and created an initial version of the toolkit. Empirical work (51 in-depth interviews, 1 focus group, 2 case studies in India and the Philippines) conducted in 2018 and 2019 then tested those findings against information from global health research practice. The final ethical toolkit is a reflective project planning aid. It consists of 4 worksheets (Worksheet 1- Selecting Partners; Worksheet 2- Deciding to Partner; Worksheet 3- Deciding to Engage with the Wider Community; Worksheet 4- Designing Priority-setting) and a Companion Document detailing how to use them. Reflecting on and discussing the questions in Worksheets 1 to 4 before priority-setting will help deliver priority-setting processes that share power with communities and projects with research topics and questions that more accurately reflect their healthcare and system needs.

摘要

为了促进社会公正和平等,全球卫生研究应在项目过程中让社区有意义地参与进来:从设定议程开始。但是,社区,尤其是那些被认为处于不利地位或边缘化的社区,在旨在帮助他们的研究项目的优先事项方面几乎没有发言权。迄今为止,关于如何在卫生研究优先事项设定中与社区分享权力,仍然缺乏有限的道德指导和资源。本文为学术研究人员及其社区合作伙伴提供了一个“道德工具包”,用于设计有意义地纳入受项目影响的社区的优先事项设定过程。采用实证反思平衡方法来开发工具包。概念性工作阐明了在全球卫生研究优先事项设定中分享权力的道德考虑因素,制定了如何解决这些问题的指导意见,并创建了工具包的初始版本。2018 年和 2019 年进行的实证工作(51 次深入访谈、1 次焦点小组、印度和菲律宾的 2 个案例研究)然后根据全球卫生研究实践中的信息对这些发现进行了测试。最终的道德工具包是一个反思性项目规划辅助工具。它由 4 个工作表(工作表 1-选择合作伙伴;工作表 2-决定合作;工作表 3-决定与更广泛的社区接触;工作表 4-设计优先事项设定)和一份详细说明如何使用它们的配套文件组成。在进行优先事项设定之前,对工作表 1 至 4 中的问题进行反思和讨论,将有助于实施与社区分享权力的优先事项设定过程,并使研究主题和问题更准确地反映其医疗保健和系统需求的项目。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fd/8145852/eb26bd1de206/12939_2021_1453_Fig1_HTML.jpg

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