Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/30045
Title: Understanding dementia in minority ethnic communities: The perspectives of key stakeholders interviewed as part of the IDEAL programme
Authors: Victor, CR
van den Heuvel, E
Pentecost, C
Quinn, C
Charlwood, C
Clare, L
Keywords: ethnicity;understanding dementia;belonging;racism;responding to dementia;the migrant lifecourse
Issue Date: 16-Aug-2024
Publisher: SAGE Publications
Citation: Victor, C.R. et al. (2024) 'Understanding dementia in minority ethnic communities: The perspectives of key stakeholders interviewed as part of the IDEAL programme', Dementia, 23 (7), pp. 1172 - 1182. doi: 10.1177/14713012241272817.
Abstract: Future populations of older adults in the UK, those aged 65+, will demonstrate increased diversity in terms of their ethnic identity resultant from the ageing of the post-war migrants from India, Pakistan, Bangladesh, and the Caribbean. As a consequence, there will be an increase in the numbers of older adults from these communities living with age-related chronic diseases such as dementia. In response to these demographic changes, we need to develop a research, policy and practice agenda that is inclusive and provides evidence for the development of culturally diverse and effective models of service delivery. This requires engagement with three key stakeholder groups: (a) people with dementia; (b) their carers; and (c) the wider community. As part of the IDEAL research programme on living well with dementia, we undertook semi-structured interviews with twelve community leaders, defined as known and trusted individuals active in their respective communities, and six community members (two people living with dementia and four carers). We explored their understandings, experiences, and views of about dementia. Our analysis identified two overarching themes. The migrant lifecourse highlighted issues of not belonging, discrimination and racism. This framed our second theme, the cultural context of dementia, which addressed dementia knowledge and attitudes, service provision and service access, and how being part of a minority ethnic community made a difference to these experiences. Our study highlights how lifecourse experiences of negative hostile social and policy environments and services can be profound and long-lasting and provide a prism through which accessing dementia care is experienced. Our findings argue for the inclusion of diverse views and lifecourse experiences within the context of developing a dementia strategy for research, policy and practice that is appropriate for a multicultural and heterogenous society.
Description: Data availability statement: The data that support the findings of this study are available from the corresponding author upon reasonable request.
URI: https://bura.brunel.ac.uk/handle/2438/30045
DOI: https://doi.org/10.1177/14713012241272817
ISSN: 1471-3012
Other Identifiers: ORCiD: Christina R. Victor https://orcid.org/0000-0002-4213-3974
ORCiD: Eleanor van den Heuvel https://orcid.org/0000-0003-3603-2576
ORCiD: Claire Pentecost https://orcid.org/0000-0003-2048-5538
ORCiD: Catherine Quinn https://orcid.org/0000-0001-9553-853X
ORCiD: Catherine Charlwood https://orcid.org/0000-0002-3522-8457
ORCiD: Linda Clare https://orcid.org/0000-0003-3989-5318
Appears in Collections:Dept of Health Sciences Research Papers

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