Introduction Clinical research focused on aging, Alzheimer's disease and related dementias
(ADRD), and caregiving often does not recruit Asian Americans and Pacific Islanders …

The aims of this paper are to illustrate the trend towards data sharing, ie the regulated
availability of the original patient-level data obtained during a study, and to discuss the …

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 …

Importance Black or African American (hereinafter, Black) and Hispanic or Latino/a/x
(hereinafter, Latinx) adults are disproportionally affected by Alzheimer disease, but most …

Abstract Background Although Black/African American older adults bear significant
inequities in prevalence, incidence, and outcomes of Alzheimer's disease and related …

Abstract Introduction This study elicited Asian Americans and Pacific Islanders'(AAPI)
perspectives about recruitment strategies/messaging for participation in an aging …

Participant registries are repositories of individuals who have expressed willingness to learn
about studies for which they may be eligible. Registries are increasingly being used to …

Background Recruitment in sexual health research is challenging. This study explores the
potential of a Consent for Contact system (C4C)-generic consent for research contact-to …

Research registries are a powerful tool for boosting recruitment into clinical trials. However,
little is known about how parents approach the decision to enroll their child in a pediatric …

Background: Registries have been proposed as a novel way to accelerate targeted
recruitment for Alzheimer disease prevention clinical trials. However, there are limited data …