Mozersky Jessica, Dimtsu Assfaw Araya, Balls Berry Joyce E, Moulder Krista L, Denny Andrea, Aranda María, Asthana Sanjay, Babulal Ganesh, Berry Beverly, Boyd Amanda, Buchwald Dedra, Croff Raina, Flatt Jason, Gabel Mattew, Gleason Carey E, Glover Crystal M, Green-Harris Gina, Hudson Darrell, Jackson Jonathan, Johnson David K, Medina Luis, Mendez Scarlet, O'Bryant Sid, Park Van Ta, Parker Monica W, Petty Douglass, Stites Shana D, Streitz Marissa L, Ushe Mwiza, Wilkins Consuelo H, Zuelsdorff Megan, Morris John C
Knight Alzheimer Disease Research Center, Washington University in St Louis, St Louis, Missouri, USA.
Alzheimer's Disease Research Center, Alzheimer's Disease Resource Center for Minority Aging Research, Suzanne Dworak-Peck School of Social Work, Edward R. Roybal Institute on Aging Los Angeles, University of Southern California, Los Angeles, California, USA.
Alzheimers Dement. 2025 May;21(5):e70168. doi: 10.1002/alz.70168.
This paper reports on a Conference organized by the Washington University School of Medicine's (WUSM) Knight Alzheimer Disease Research Center (Knight ADRC), entitled "Enhancing Participation by Minoritized Groups in Alzheimer Disease and Related Dementia (ADRD) Research." It builds on recommendations from a 2018 Workshop. Representatives from all 37 federally funded ADRCs described strategies to enhance the recruitment and engagement of participants from historically minoritized groups. St. Louis community members attended and provided input. The Conference was guided by the 2015 National Institute on Aging (NIA) Health Disparities Research Framework, which delineates that "fundamental life-course factors such as race, ethnicity, and socioeconomic status interact with behavioral and biological characteristics to determine health and disease." The multiple ways of engaging participants described at the Conference provide guidance and strategies that can be adapted and utilized across the ADRC network and other research programs nationally to enhance inclusion of minoritized groups in ADRD research. Highlights Increasing representation in Alzheimer disease and related dementias (ADRD) research is a national priority. The National Conference described strategies to diversify participation in AD research. All Alzheimer's Disease Research Centers (ADRCs) were represented. Local community members attended and participated in breakout sessions. Many community-engaged strategies are being used to enhance recruitment and retention. Approaches can be adapted for local needs and utilized by ADRCs.
本文报道了由华盛顿大学医学院(WUSM)的奈特阿尔茨海默病研究中心(Knight ADRC)组织的一次会议,会议主题为“提高少数族裔群体对阿尔茨海默病及相关痴呆症(ADRD)研究的参与度”。它基于2018年一次研讨会的建议。来自所有37个由联邦政府资助的ADRC的代表描述了提高历史上少数族裔群体参与者招募和参与度的策略。圣路易斯社区成员出席并提供了意见。该会议以2015年美国国立衰老研究所(NIA)的健康差异研究框架为指导,该框架指出“种族、民族和社会经济地位等基本生命历程因素与行为和生物学特征相互作用,以决定健康和疾病”。会议上描述的多种吸引参与者的方式提供了可在ADRC网络以及全国其他研究项目中进行调整和利用的指导和策略,以提高少数族裔群体在ADRD研究中的参与度。要点在阿尔茨海默病及相关痴呆症(ADRD)研究中增加代表性是一项国家优先事项。全国会议描述了使AD研究参与多样化的策略。所有阿尔茨海默病研究中心(ADRC)均有代表出席。当地社区成员出席并参加了分组讨论。许多社区参与策略正在被用于加强招募和留用。这些方法可根据当地需求进行调整并由ADRC使用。