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首页> 外文期刊>BMC Medical Ethics >Exploring researchers’ experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study
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Exploring researchers’ experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics study

机译:在南非精神分裂症基因组学研究中探索研究人员与研究人员驱动,针对特定人群的社区咨询委员会合作的经验

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Background Community engagement within biomedical research is broadly defined as a collaborative relationship between a research team and a group of individuals targeted for research. A Community Advisory Board (CAB) is one mechanism of engaging the community. Within genomics research CABs may be particularly relevant due to the potential implications of research findings drawn from individual participants on the larger communities they represent. Within such research, CABs seek to meet instrumental goals such as protecting research participants and their community from research-related risks, as well as intrinsic goals such as promoting the respect of participants and their community. However, successful community engagement depends on the degree to which CABs legitimately represent and engage with communities targeted for research. Currently, there is little literature describing the use of CABs in genomics research taking place in developing countries, and even less in the field of genomics research relating to mental illness. The aim of this article is to describe and consider the contributions made by a researcher-driven, population-specific CAB in a genomics of schizophrenia research project taking place in South Africa, from the perspective of the research team. Discussion Four broad discussion topics emerged during the CAB meetings namely: 1) informed consent procedures, 2) recruitment strategies, 3) patient illness beliefs and stigma experiences, and 4) specific ethical concerns relating to the project. The authors consider these discussions in terms of their contributions to instrumental and intrinsic goals of community engagement. Summary The CAB gave valuable input on the consent processes and materials, recruitment strategies and suggested ways of minimizing the potential for stigma and discrimination. All of these contributions were of an instrumental nature, and helped improve the way in which the research took place. In addition, and perhaps more importantly, the CAB made a unique and important contribution relating to intrinsic functions such as promoting the respect and dignity of research participants and their community. This was particularly evident in ensuring sensitivity and respect of the community’s traditional beliefs about schizophrenia and its treatment, and in this way promoting a respectful relationship between the research team and the participants.
机译:背景技术生物医学研究中的社区参与被广泛定义为研究团队与一组研究对象之间的协作关系。社区咨询委员会(CAB)是一种与社区互动的机制。在基因组学研究中,CAB可能特别相关,因为从单个参与者那里获得的研究结果可能会对潜在的更大社区产生潜在影响。在此类研究中,CAB寻求实现工具性目标,例如保护研究参与者及其社区免受与研究相关的风险,以及内在目标,例如促进对参与者及其社区的尊重。但是,成功的社区参与取决于CAB合法代表和参与研究社区的程度。当前,很少有文献描述在发展中国家进行的基因组学研究中使用CAB的情况,而在有关精神疾病的基因组学研究领域则更少。本文的目的是从研究团队的角度描述和考虑由研究人员驱动的针对特定人群的CAB在南非发生的精神分裂症基因组研究项目中的贡献。讨论在CAB会议期间出现了四个广泛的讨论主题,即:1)知情同意程序,2)招聘策略,3)患者疾病的信念和污名化经历以及4)与项目有关的特定道德问题。作者根据对社区参与的工具性和内在目标的贡献来考虑这些讨论。总结CAB在同意过程和材料,招聘策略以及减少污名化和歧视的可能性方面提供了宝贵的意见。所有这些贡献都是工具性的,有助于改善研究的方式。此外,也许更重要的是,CAB在诸如促进研究参与者及其社区的尊重和尊严等内在功能方面做出了独特而重要的贡献。在确保敏感性和尊重社区关于精神分裂症及其治疗的传统观念方面,这尤其明显,从而促进了研究团队与参与者之间的尊重关系。

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