Vidoni Eric D, Swinford Emma, Barton Kelli, Perales-Puchalt Jaime, Niedens C Michelle, Lewandowski Tina, Schwasinger-Schmidt Tiffany, Peltzer Jill, Wurth JoEllen, Berkley-Patton Jannette, Townley Ryan A, Moore W Todd, Shaw Ashley R, Key Mickeal N, Andrade Erica, Robinson Melissa, Sprague Susan, Bondurant Aiden, Brook Debra, Freund Jennifer, Burns Jeffrey M
University of Kansas Alzheimer's Disease Research Center University of Kansas Medical Center Fairway Kansas USA.
Institute for Human Development University of Missouri Kansas City Kansas City Missouri USA.
Alzheimers Dement (N Y). 2024 Jun 20;10(2):e12475. doi: 10.1002/trc2.12475. eCollection 2024 Apr-Jun.
Recruitment of sufficient and diverse participants into clinical research for Alzheimer's disease and related dementias remains a formidable challenge. The primary goal of this manuscript is to provide an overview of an approach to diversifying research recruitment and to provide case examples of several methods for achieving greater diversity in clinical research enrollment.
The University of Kansas Alzheimer's Disease Research Center (KU ADRC) developed MyAlliance for Brain Health (MyAlliance), a service-oriented recruitment model. MyAlliance comprises a Primary Care Provider Network, a Patient and Family Network, and a Community Organization Network, each delivering tailored value to relevant parties while facilitating research referrals.
We review three methods for encouraging increased diversity in clinical research participation. Initial outcomes reveal an increase in underrepresented participants from 17% to 27% in a research registry. Enrollments into studies supported by the research registry experienced a 51% increase in proportion of participants from underrepresented communities.
MyAlliance shifts power, resources, and knowledge to community advocates, promoting brain health awareness and research participation, and demands substantial financial investment and administrative commitment. MyAlliance offers valuable lessons for building sustainable, community-centered research recruitment infrastructure, emphasizing the importance of localized engagement and cultural understanding.
MyAlliance led to a significant increase in the representation of underrepresented racial and ethnic groups and individuals from rural areas.The service-oriented approach facilitated long-term community engagement and trust-building, extending partnerships between an academic medical center and community organizations.While effective, MyAlliance required substantial financial investment, with costs including infrastructure development, staff support, partner organization compensation, and promotional activities, underscoring the resource-intensive nature of inclusive research recruitment efforts.
为阿尔茨海默病及相关痴呆症的临床研究招募足够数量且多样化的参与者仍然是一项艰巨的挑战。本手稿的主要目标是概述一种使研究招募多样化的方法,并提供几个在临床研究入组中实现更大多样性的方法的案例。
堪萨斯大学阿尔茨海默病研究中心(KU ADRC)开发了脑健康联盟(MyAlliance),这是一种以服务为导向的招募模式。MyAlliance由一个初级保健提供者网络、一个患者及家庭网络和一个社区组织网络组成,每个网络都为相关方提供量身定制的价值,同时促进研究推荐。
我们回顾了三种鼓励临床研究参与度提高多样性的方法。初步结果显示,在一个研究登记处中,代表性不足的参与者比例从17%增加到了27%。由该研究登记处支持的研究的入组中,来自代表性不足社区的参与者比例增加了51%。
MyAlliance将权力、资源和知识转移给社区倡导者,提高了脑健康意识和研究参与度,并且需要大量的资金投入和行政承诺。MyAlliance为建立可持续的、以社区为中心的研究招募基础设施提供了宝贵的经验教训,强调了本地化参与和文化理解的重要性。
MyAlliance使代表性不足的种族和族裔群体以及农村地区个人的代表性显著增加。这种以服务为导向的方法促进了长期的社区参与和信任建立,扩展了学术医疗中心与社区组织之间的伙伴关系。虽然有效,但MyAlliance需要大量资金投入,成本包括基础设施建设、人员支持、合作伙伴组织补偿和推广活动,突显了包容性研究招募工作资源密集的性质。