A Mini-Review of Strategies for Recruiting Older African Americans to Alzheimer's Disease Research.

Community health equity research & policy Pub Date : 2024-07-01 Epub Date: 2022-09-18 DOI:10.1177/0272684X221118493
Darlingtina Esiaka, Christina C Yarborough, Bernadette A Fausto, Mark A Gluck
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Abstract

African Americans experience higher incidence and prevalence of Alzheimer's disease (AD). Yet, they continue to be underrepresented in AD research, limiting the ability to generalize findings to the increasingly diverse US population. To reduce AD disparities, targeted efforts are needed to increase the representation of African Americans in AD research. This mini review identified evidence-based strategies that increased research participation among older African Americans. Four recruitment strategies emerged from eight published peer-reviewed studies that directly evaluated the effectiveness of strategies aimed at increasing the number of African American participants in Alzheimer's research. The strategies include community outreach and education, face-to-face discussions, remote access, and referral and partnership with local organizations. Across different locations, these strategies increased the number of African Americans enrolled into AD research, the number of people that signed up to donate their brains for AD research upon death, and the knowledge and perception of AD in the communities. Targeted efforts are effective in increasing AD research participation among older African Americans, especially when combined with approaches that emphasize transparency and mutual trust and involve the community as stakeholders in the research process.

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招募老年非裔美国人参与阿尔茨海默病研究的策略小型回顾。
非裔美国人的阿尔茨海默病(AD)发病率和患病率都较高。然而,他们在老年痴呆症研究中的代表性仍然不足,这限制了将研究结果推广到日益多样化的美国人口的能力。为了减少阿兹海默症的差异,需要有针对性地努力提高非裔美国人在阿兹海默症研究中的代表性。本微型综述确定了增加非裔美国老年人参与研究的循证策略。八项已发表的同行评审研究直接评估了旨在增加参与阿尔茨海默病研究的非裔美国人人数的策略的有效性,从中总结出四项招募策略。这些策略包括社区宣传和教育、面对面讨论、远程访问以及转介和与当地组织合作。在不同的地方,这些策略增加了参与阿兹海默症研究的非裔美国人的数量,增加了签约在死后捐献大脑用于阿兹海默症研究的人数,也增加了社区对阿兹海默症的了解和认知。有针对性的努力能有效提高非裔美国老年人对注意力缺失症研究的参与度,尤其是与强调透明度和相互信任以及让社区作为利益相关者参与研究过程的方法相结合时。
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