Background Disparities in clinical research participation perpetuate broader health
disparities. Recruitment registries are novel tools to address known challenges in accrual to …

INTRODUCTION Alzheimer's‐focused participant recruitment registries are tools for
accelerating enrollment into studies, however, registry members are primarily White women …

Introduction Alzheimer's disease and related dementias (ADRD) disproportionately impact
racial and ethnic minority and socioeconomically disadvantaged adults. Yet, these …

Potential participant registries are tools to address the challenge of slow recruitment to
clinical research. In particular, registries may aid recruitment to secondary prevention clinical …

Alzheimer disease (AD) research faces challenges to successful enrollment, especially to
clinical trials and biomarker studies. Failure to recruit the planned number of participants in a …

We describe the history, development, and success of the recruitment and screening
procedures used by researchers at the University of California, Davis Alzheimer's Disease …

Abstract Background Recruitment for Alzheimer's disease (AD)-focused studies, particularly
prevention studies, is challenging due to the public's lack of awareness about study …

Background Alzheimer's disease and related dementias (AD) disproportionately impact
disadvantaged populations, including racial/ethnic minorities and those from low …

Background It is widely understood that dementia researchers need to do more to foster
diversity and equitable access to research participation for underserved groups (eg …

Clinical Alzheimer's disease (AD) trials currently face a critical shortfall of thousands of
eligible participants, which inflates the duration and cost of the clinical study as well as …