Recruit & Retain Participants

This article highlights how concentrated community memory screening events can be an effective and efficient recruitment strategy for Alzheimer’s disease research.

Researchers assessed direct-to-consumer APOE genetic testing usage and their attitudes toward using this information in clinical trial recruitment.

This paper describes the researchers’ experiences in establishing and maintaining a diverse Alzheimer’s Disease Prevention Registry.

A report that overviews the Washington University School of Medicine Knight ADRC's “African American Participation in Alzheimer Disease Research: Effective Strategies” Workshop on research participation.

This research examined the effectiveness and differences in using both traditional and social media materials for the recruitment of African American versus non-Hispanic white participants.

This research article describes the Minority Aging Research Study's brain donation challenges, processes, and successful procurement with older African American adults.

The CARE registry is addressing the gap and disparities in research participation among Asian Americans and Pacific Islanders and encourages participating in research.

Dr. Jonathan Jackson and the Massachusetts Alzheimer’s Disease Research Center give a webinar about direct actions researchers can take to improve diversity and equity in clinical research studies.

In this two-page flyer, a healthy participant who does not have Alzheimer’s disease describes why he decided to participate in Alzheimer’s research.

The Massachusetts Alzheimer’s Disease Research Center offers an eight-page handout and presentation on participating in Alzheimer’s disease clinical research.