“You just can’t do that in dementia care”: Barriers to partnership working within dementia services for people from South Asian communities

Cheston, Richard; Dodd, Emily; Smith, P; Woodstoke, Natasha S.; Jutlla, K; Fry, G; Truswell, D; Butt, J; Parveen, S

Abstract

Background: People from South Asian communities are under-represented at all levels of dementia services. Consequently, there is pressure for the statutory sector to deliver services in partnership with Voluntary, Community, Faith and Social Enterprises (VCFSEs). This study set out to explore the constraints to effective partnership working which prevent dementia care from being delivered in an equitable way.
Methods: Data collection consisted of two phases. First, we interviewed seven people with experience of partnership working and developed three fictional vignettes that were representative of the challenges they faced. We then used these vignettes to stimulate discussion in focus groups and interviews with 13 VCFSE and 16 statutory sector participants. Data was analysed using deductive thematic analysis.
Findings: Three themes were developed during the analysis. First, White British-centric services focused on the challenges for statutory services in meeting the needs of South Asians, developing flexible, responsive services and making inclusive partnership working truly meaningful. Second, VCFSE participants (but not statutory service participants) associated a failure to deliver effective partnership working with unconscious bias operating within systems, leading to the devaluing of their expertise and to their views being ignored. Finally, participants emphasised the need to prioritise relationships if they were to meet the challenges of developing partnership working.
Conclusion: We identified three constraints acting to prevent effective partnership working. First, the different meanings that statutory and VCFSE participants attach to challenges threatens their ability to develop a shared understanding of the needs of communities. Second, a reluctance to explicitly address service deficiencies can mean that stereotypes remain unaddressed. Finally, while both parties lacked power to change the fundamentals of service delivery, power and resources were also unbalanced with VCSFE services being more reliant on the statutory sector.

• Journal Article Type: Article
• Acceptance Date: Aug 29, 2024
• Online Publication Date: Sep 14, 2024
• Deposit Date: Sep 16, 2024
• Publicly Available Date: Sep 23, 2024
• Journal: Dementia: The International Journal of Social Research and Practice
• Print ISSN: 1471-3012
• Electronic ISSN: 1741-2684
• Publisher: SAGE Publications
• Peer Reviewed: Peer Reviewed
• DOI: https://doi.org/10.1177/14713012241283189
• Keywords: minority health, Alzheimer’s disease, voluntary health agencies, caregivers, accessibility of health services, community health care
• Public URL: https://uwe-repository.worktribe.com/output/12889707