2023
DOI: 10.1002/alz.13077
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Brain health registry updates: An online longitudinal neuroscience platform

Abstract: IntroductionRemote, internet‐based methods for recruitment, screening, and longitudinally assessing older adults have the potential to facilitate Alzheimer's disease (AD) clinical trials and observational studies.MethodsThe Brain Health Registry (BHR) is an online registry that includes longitudinal assessments including self‐ and study partner‐report questionnaires and neuropsychological tests. New initiatives aim to increase inclusion and engagement of commonly underincluded communities using digital, commun… Show more

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Cited by 6 publications
(12 citation statements)
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“…These rates are substantially higher than those of other BHR surveys. 9 Still, the drop-off from 3565 study invitations to 288 individuals enrolled (8% of those invited) suggests that there may be study selection biases and emphasizes the need for caution regarding CDR scalability in other settings.…”
Section: Discussionmentioning
confidence: 99%
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“…These rates are substantially higher than those of other BHR surveys. 9 Still, the drop-off from 3565 study invitations to 288 individuals enrolled (8% of those invited) suggests that there may be study selection biases and emphasizes the need for caution regarding CDR scalability in other settings.…”
Section: Discussionmentioning
confidence: 99%
“…Participants and study partners completed the eCDR in-clinic at their baseline visit without assistance and then were instructed to complete the eCDR remotely, through the BHR online portal, within 2 weeks of the initial in-clinic administration (eAppendix 1 in Supplement 1). The mean (SD) time to complete the eCDR was 12.0 (3.4) minutes for participants and 16.0 (2.1) minutes for study partners.…”
Section: Methodsmentioning
confidence: 99%
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“…[3][4][5] In the ADRD field, several registries exist that differ in terms of reach (e.g., local vs national), population of interest, and format. [6][7][8][9][10][11][12][13][14][15] One of the priorities outlined in the "National Strategy for Recruitment and Participation in Alzheimer's Disease Clinical Research" is the assessment of registry performance. 16 Registry performance metrics include but are not limited to, registry enrollment, registry engagement (e.g., baseline and longitudinal assessment completion), and referral success to other studies.…”
Section: Introductionmentioning
confidence: 99%