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非裔美国人参与阿尔茨海默病临床研究障碍的根本原因。

Fundamental causes of barriers to participation in Alzheimer's clinical research among African Americans.

机构信息

Suzanne Dworak-Peck School of Social Work, University of Southern California, Los Angeles, CA, USA.

Alzheimer's Therapeutic Research Institute, University of Southern California, San Diego, CA, USA.

出版信息

Ethn Health. 2021 May;26(4):585-599. doi: 10.1080/13557858.2018.1539222. Epub 2018 Oct 30.

Abstract

African Americans have a significantly higher risk than Whites for developing Alzheimer's disease (AD), but show lower participation in AD clinical trials. Studies of African Americans' involvement in clinical research have identified fear and mistrust of research as barriers to participation. Historical occurrences of unethical research practices are often cited as the source of these attitudes, but underlying factors such as African Americans' experiences of racism and discrimination remain unexplored. The goal of this study was to examine the roles of race and culture in the attitudes and beliefs of African Americans about participating in clinical research. Five focus groups were conducted with 44 African American men and women (aged 50 and over) in a western U.S. state. Participants were asked scripted questions regarding their knowledge and beliefs about AD and their feelings about participating in clinical research. A taxonomy was created to organize results based on participant responses. Four major thematic clusters emerged that influence African Americans beliefs about and participation in clinical research: (a) experiences of unequal treatment and racism, (b) cultural trauma due to historical events and contemporary experiences, (c) racial identity and cultural norms, and (d) the importance of cultural competency and racial congruence in recruitment and research studies. Understanding, acknowledging, and addressing the factors that underlie mistrust and fear of research is important to build trust and to develop culturally appropriate outreach, education, and recruitment strategies that will increase African Americans' participation in clinical research.

摘要

非裔美国人患老年痴呆症(AD)的风险明显高于白人,但参与 AD 临床试验的比例较低。对非裔美国人参与临床研究的研究表明,对研究的恐惧和不信任是参与的障碍。人们经常将不道德的研究行为的历史事件作为这些态度的根源,但种族主义和歧视等潜在因素仍未得到探索。本研究的目的是检验种族和文化在非裔美国人对参与临床研究的态度和信念中的作用。在美国西部的一个州,对 44 名年龄在 50 岁及以上的非裔美国男性和女性进行了 5 个焦点小组的访谈。参与者被问到有关他们对 AD 的知识和信仰以及对参与临床研究的感受的脚本问题。创建了一个分类法来根据参与者的回答组织结果。出现了四个主要的主题集群,影响了非裔美国人对临床研究的信念和参与:(a)不平等对待和种族主义的经历,(b)历史事件和当代经历造成的文化创伤,(c)种族身份和文化规范,以及(d)在招募和研究中注重文化能力和种族一致性的重要性。了解、承认和解决不信任和对研究的恐惧的根源,对于建立信任以及制定文化上适当的外联、教育和招募策略,以增加非裔美国人参与临床研究的比例非常重要。

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