The Alzheimer’s Prevention Registry: A Large Internet-Based Participant Recruitment Registry to Accelerate Referrals to Alzheimer’s-Focused Studies - 21/11/24

Doi : 10.14283/jpad.2020.31 
Jessica B. Langbaum 1, 5, 8, , , N. High 1, J. Nichols 1, 2, C. Kettenhoven 1, E.M. Reiman 1, 3, 4, 6, 7, 8, P.N. Tariot 1, 4, 8
1 Banner Alzheimer’s Institute, 901 E. Willetta Street, 85006, Phoenix, AZ, USA 
2 Midwestern University, Glendale, AZ, USA 
3 Neurodegenerative Disease Research Center, Arizona State University, Tempe, AZ, USA 
4 Department of Psychiatry, University of Arizona College of Medicine, Phoenix, AZ, USA 
5 Department of Neurology, University of Arizona College of Medicine, Phoenix, AZ, USA 
6 Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ, USA 
7 Biodesign Institute, Arizona State University, Tempe, AZ, USA 
8 Arizona Alzheimer’s Consortium, Phoenix, AZ, USA 

a Jessica.Langbaum@bannerhealth.com

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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 opportunities coupled with studies’ inclusion and exclusion criteria, resulting in a high screen fail rate.

Objectives

To develop an internet-based participant recruitment registry for efficiently and effectively raising awareness about AD-focused study opportunities and connecting potentially eligible volunteers to studies in their communities.

Methods

Individuals age 18 and older are eligible to join the Alzheimer’s Prevention Registry (APR). Individuals provide first and last name, year of birth, country, and zip/postal code to join the APR; for questions regarding race, ethnicity, sex, family history of AD or other dementia, and diagnosis of cognitive impairment, individuals have the option to select “prefer not to answer.” The APR website maintains a list of recruiting studies and contacts members who have opted in by email when new studies are available for enrollment.

Results

As of December 1, 2019, 346,661 individuals had joined the APR. Members had a mean age of 63.3 (SD 11.7) years and were predominately women (75%). 94% were cognitively unimpaired, 50% reported a family history of AD or other dementia, and of those who provided race, 76% were white. 39% joined the APR as a result of a paid social media advertisement. To date, the APR helped recruit for 82 studies.

Conclusions

The APR is a large, internet-based participant recruitment registry designed to raise awareness about AD prevention research and connect members with enrolling studies in their communities. It has demonstrated the ability to recruit and engage a large number of highly motivated members and assist researchers in meeting their recruitment goals. Future publications will report on the effectiveness of APR for accelerating recruitment and enrollment into AD-focused studies.

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Key words : Registry, recruitment, Alzheimer’s disease


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Vol 7 - N° 4

P. 242-250 - Settembre 2020 Ritorno al numero
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