Transcending inequities in dementia care in Black communities: Lessons from the maximizing independence at home care coordination program.

community-based dementia care dementia care coordination dementia care in Black American populations dementia caregiving equity in dementia care

Journal

Dementia (London, England)
ISSN: 1741-2684
Titre abrégé: Dementia (London)
Pays: England
ID NLM: 101128698

Informations de publication

Date de publication:
Jul 2022
Historique:
pubmed: 1 6 2022
medline: 28 6 2022
entrez: 31 5 2022
Statut: ppublish

Résumé

We examine care partners' experience of the Maximizing Independence at Home (MIND) intervention, a multicomponent, home-based dementia care coordination program designed to provide high quality, wholistic care coordination for people and families living with dementia. The goal of the study was to understand 1. the unique dementia-related needs of Black care partners and barriers and challenges to caregiving experienced within the Black community, 2. perceived benefits of the MIND program, and 3. ways to improve the program and make it more culturally responsive to the Black community. We conducted three focus groups totaling 20 care partners of people living with dementia; who participated in the MIND intervention (2014-2019); all Black/African American and English speaking. Verbatim transcriptions were independently analyzed line-by-line by two coders using inductive approaches. Participants noted three overarching themes related to dementia care needs and challenges in the Black community: difficulty finding and accessing dementia information and relevant services and supports; familial conflict/lack of sibling and familial support; and lack of effective communication about dementia within Black Communities. Regarding MIND at home program benefits, four themes emerged: 1. perceived to help locate resources (formal and informal); 2. provided care partners an opportunity for socialization and interaction; 3. included comprehensive assessments and helpful linked information; and 4. resulted in a "much needed break for care partners." Increased diversity of the MIND program personnel, greater clarity and consistency in MIND program promotion, and better communications were themes for how the program could be improved. Care partners participating in the MIND program perceived common benefits in aspects related to care for the persons living with dementia as well as benefits to themselves, believed the program addressed important challenges and gaps in education, services, and social support, and could be enhanced in its delivery and cultural responsiveness.

Identifiants

pubmed: 35634792
doi: 10.1177/14713012221085808
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1653-1668

Subventions

Organisme : NIA NIH HHS
ID : R01 AG046274
Pays : United States

Auteurs

Danetta H Sloan (DH)

Department of Health, Behavior and Society, 25802Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Deirdre Johnston (D)

Department of Psychiatry and Behavioral Sciences, 1500Johns Hopkins School of Medicine, Baltimore, MD, USA.

Chanee Fabius (C)

Department of Health, Policy and Management, 25802Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Tabitha Pyatt (T)

Department of Mental Health, 25802Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

Inga Antonsdottir (I)

Department of Psychiatry and Behavioral Sciences, 1500Johns Hopkins School of Medicine, Baltimore, MD, USA; 15851Johns Hopkins School of Nursing, Baltimore, MD, USA.

Melissa Reuland (M)

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA15851.

Morgan Spliedt (M)

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA15851.

Quincy M Samus (QM)

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA15851.

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Classifications MeSH