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招募原住民患者参与临床试验:建立信任圈。

Recruiting Indigenous Patients Into Clinical Trials: A Circle of Trust.

机构信息

Department of Community Health and Family Medicine, University of Florida, Gainesville, Florida

Department of Health Services Research, Management and Policy, University of Florida, Gainesville, Florida.

出版信息

Ann Fam Med. 2023 Jan-Feb;21(1):54-56. doi: 10.1370/afm.2901.

Abstract

The Circle of Trust is a new conceptual model that can help investigators and the American Indian/Alaska Natives (AI/AN) community work together to promote inclusion of AI/AN populations in clinical trials to improve health outcomes. Racial/ethnic minority groups remain underrepresented in clinical trials and this creates the need and opportunity for novel approaches. Indigenous populations are particularly underrepresented in clinical trials. Studies show that AI/AN have the lowest representation of race/ethnic groups in the United States. American Indian/Alaska Natives suffer from significant health disparities with higher rates of morbidity and mortality and lower rates for preventative measures and access to health services. A variety of barriers to recruitment of minority patients exist at several levels including the system/institutional, interpersonal, and the individual. The authors, experts in AI/AN health and recruitment of minorities into research, collaborated to modify the currently existing and published "trust triangle" model that focuses on minority recruitment to include participants, researcher, and trusted entity. We advocate for expanding the trust triangle into a circle of trust inclusive of community. The "circle of trust" is a new conceptual model that can help investigators and the AI/AN community work together to promote inclusion of AI/AN populations in clinical trials to improve health outcomes.

摘要

信任圈是一个新的概念模型,可以帮助研究人员和美国印第安人/阿拉斯加原住民(AI/AN)社区合作,共同促进将 AI/AN 人群纳入临床试验,以改善健康结果。在临床试验中,少数族裔群体仍然代表性不足,这就需要并提供了新的方法。在临床试验中,土著人群的代表性尤其不足。研究表明,AI/AN 是美国各族裔中代表性最低的群体。美国印第安人/阿拉斯加原住民面临着严重的健康差距,发病率和死亡率较高,预防措施和获得医疗服务的机会较低。在多个层面上,包括系统/机构、人际和个人层面,都存在着招募少数族裔患者的各种障碍。作者是 AI/AN 健康和少数族裔参与研究方面的专家,他们合作修改了目前现有的和已发表的“信任三角”模型,该模型侧重于少数族裔的招募,包括参与者、研究人员和可信赖的实体。我们主张将信任三角扩展为一个包含社区的信任圈。“信任圈”是一个新的概念模型,可以帮助研究人员和 AI/AN 社区合作,共同促进将 AI/AN 人群纳入临床试验,以改善健康结果。

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