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Community Input for Addressing Dementia Health Disparities

Richmond Brain Health Initiative

Bibliographic Data

ID6446388
AuthorsFaika Zanjani (0000-0001-5808-6116), Annie Rhodes (0000-0002-3097-918X), Kelsey O’donnell (0000-0002-2264-3889), Kennedy O'Donnell, Cate Hawks, Peter A Boling, Peter Boling, Patricia W Slattum (0000-0003-1858-5089), Elvin T Price (0000-0001-6046-7540), Elvin Price (0000-0001-7991-6430), Pamela Parsons (0000-0001-8839-3336), Kathie Falls, Natalie Mansion (0009-0000-5180-2239), Ana F Diallo (0000-0003-1547-2062), Ana Diallo, Kimberely Battle, Sarah Hobgood, Leland Waters (0000-0003-2537-102X), Tracey Gendron (0000-0001-8975-2302), Emily Atkinson (0000-0003-0072-3287), Matthew Jones (0000-0002-9272-5687), Katie Mcdonoug, George Worthington, Julie Blaskewicz Boron (0000-0003-1121-8120), Christine Jensen (0000-0003-2085-9122), Brian D Berman (0000-0002-0602-9942), Lana Sargent (0000-0001-5555-9985)
Year2025
Volume19
Issue1
Pages71-83
Publication date2025-03-01
Open AccessYes
TypeARTICLE
VenueProgress in community health partnerships (JOURNAL)
Journal identifiersISSN: 1557-055X • E-ISSN: 1557-0541
PublisherJohns Hopkins University Press (PUBLISHER • US)
DOI10.1353/cpr.2025.a956599
PMID40223630
OpenAlexW4409339821
LanguageEN
Citations received1

Background: The development of the Richmond Brain Health Initiative (RBHI) was guided by the need to address local brain health service gaps to improve Alzheimer's/Dementia health disparities in racially diverse communities. This paper describes the establishment of RBHI through 1) community and provider stakeholder input and 2) community brain health screening/intake development and testing. Methods: Phase 1 involved provider and community stakeholder questionnaires to gather feedback as part of the Plan–Do–Study–Act cycle. Subsequently, stakeholder findings directed the RBHI structure and screening/intake registration testing in the community. Results: Based on the stakeholder responses from fifteen providers and twenty community members, there was strong consensus in the need for local brain health services. The most highly recommended screening needs were for caregiving, cognitive status, and lifestyle risks. Thereafter the RBHI screening/intake was developed and completed by 45 community participants. Participants showed hypertension (62%) as the most prevalent brain health risk factor, followed by depression/anxiety (56%), and loneliness (44%). The intake also indicated cognitive and functional deficits, with the Montreal Cognitive mean equaling 18.4 and the Functional Activities mean equaling 14.9. Additionally, 73% of participants reported experiencing subjective cognitive decline. Conclusions: This study showcases a model for promoting brain health in racially diverse communities to improve access to Alzheimer's disease and related dementia resources and services

Community health · Community-based participatory research · Dementia · Health equity · Participatory action research · Political science · Public health · Sociology · Health Policy Implementation Science · Medicine · Nursing · Psychology · Gerontology

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Citations per year1
Citation span2026 - 2026 (1)
Highly citedNo

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