A service‐oriented approach to clinical trial recruitment for dementia and brain health: Methods and case examples of MyAlliance for Brain Health

Author:

Vidoni Eric D.1,Swinford Emma2,Barton Kelli2,Perales‐Puchalt Jaime1,Niedens C. Michelle1,Lewandowski Tina1,Schwasinger‐Schmidt Tiffany3,Peltzer Jill1,Wurth JoEllen1,Berkley‐Patton Jannette4,Townley Ryan A.1,Moore W. Todd1,Shaw Ashley R.1,Key Mickeal N.1,Andrade Erica5,Robinson Melissa6,Sprague Susan7,Bondurant Aiden1,Brook Debra1,Freund Jennifer1,Burns Jeffrey M.1

Affiliation:

1. University of Kansas Alzheimer's Disease Research Center University of Kansas Medical Center Fairway Kansas USA

2. Institute for Human Development University of Missouri Kansas City Kansas City Missouri USA

3. Department of Internal Medicine University of Kansas School of Medicine–Wichita Wichita Kansas USA

4. Department of Biomedical and Health Informatics University of Missouri Kansas City School of Medicine Kansas City Missouri USA

5. El Centro Inc. Kansas City Kansas USA

6. Black Health Care Coalition Kansas City Missouri USA

7. OCCK Inc. Salina Kansas USA

Abstract

AbstractINTRODUCTIONRecruitment 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.METHODSThe 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.RESULTSWe 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.DISCUSSIONMyAlliance 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.Highlights 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.

Funder

National Institutes of Health

Leo and Anne Albert Charitable Trust

Publisher

Wiley

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