Accelerating diversity in Alzheimer's disease research by partnering with a community advisory board

dc.contributor.authorPena-Garcia, Alex
dc.contributor.authorRichards, Ralph
dc.contributor.authorRichards, Mollie
dc.contributor.authorCampbell, Christopher
dc.contributor.authorMosley, Hank
dc.contributor.authorAsper, Joseph
dc.contributor.authorEliacin, Johanne
dc.contributor.authorPolsinelli, Angelina
dc.contributor.authorApostolova, Liana
dc.contributor.authorHendrie, Hugh
dc.contributor.authorTackett, Andrew
dc.contributor.authorElliott, Caprice
dc.contributor.authorVan Heiden, Sarah
dc.contributor.authorGao, Sujuan
dc.contributor.authorSaykin, Andrew
dc.contributor.authorWang, Sophia
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2023-09-20T15:58:49Z
dc.date.available2023-09-20T15:58:49Z
dc.date.issued2023-05-28
dc.description.abstractIntroduction: Community advisory boards (CABs) and researcher partnerships present a promising opportunity to accelerate enrollment of underrepresented groups (URGs). We outline the framework for how the CAB and researchers at the Indiana Alzheimer's Disease Research Center (IADRC) partnered to accelerate URG participation in AD neuroimaging research. Methods: CAB and the IADRC researchers partnered to increase the CAB's impact on URG study enrollment through community and research interactions. Community interactions included the CAB collaboratively building a network of URG focused community organizations and collaborating with those URG-focused organizations to host IADRC outreach and recruitment events. Research interactions included direct impact (CAB members referring themselves or close contacts as participants) and strategic impact, mainly by the CAB working with researchers to develop and refine URG focused outreach and recruitment strategies for IADRC and affiliated studies to increase URG representation. We created a database infrastructure to measure how these interactions impacted URG study enrollment. Results: Out of the 354 URG research referrals made to the IADRC between October 2019 and December 2022, 267 referrals were directly referred by the CAB (N = 36) or from community events in which CAB members organized and/or volunteered at (N = 231). Out of these 267 referrals, 34 were enrolled in IADRC and 2 were enrolled in Indiana University Longitudinal Early Onset AD Study (IU LEADS). Of note, both studies require the prospective participants to be willing to do MRI and PET scans. As of December 2022, 30 out of the 34 enrolled participants have received a consensus diagnosis; the majority were cognitively normal (64.7%), with the remainder having mild cognitive impairment (17.6%) or early-stage AD (2.9%). Discussion: The IADRC CAB-researcher partnership had a measurable impact on the enrollment of African American/Black adults in AD neuroimaging studies. Future studies will need to test whether this conceptual model works for other sites and for other URGs.
dc.eprint.versionFinal published version
dc.identifier.citationPena-Garcia A, Richards R, Richards M, et al. Accelerating diversity in Alzheimer's disease research by partnering with a community advisory board. Alzheimers Dement (N Y). 2023;9(2):e12400. Published 2023 May 28. doi:10.1002/trc2.12400
dc.identifier.urihttps://hdl.handle.net/1805/35659
dc.language.isoen_US
dc.publisherWiley
dc.relation.isversionof10.1002/trc2.12400
dc.relation.journalAlzheimer’s & Dementia: Translational Research & Clinical Interventions
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourcePMC
dc.subjectAlzheimer's disease
dc.subjectCommunity advisory boards
dc.subjectCommunity‐engaged research
dc.subjectOutreach
dc.subjectRecruitment
dc.titleAccelerating diversity in Alzheimer's disease research by partnering with a community advisory board
dc.typeArticle
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