Evidence map›Paper›PMID 39152913›Full record

ArticleDementia (London, England)2024

Understanding dementia in minority ethnic communities: The perspectives of key stakeholders interviewed as part of the IDEAL programme.

Christina R Victor, Eleanor van den Heuvel, Claire Pentecost, Catherine Quinn, Catherine Charlwood, Linda Clare

Abstract read
In one paragraph

Article in Dementia (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Christina R VictorDepartment of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, London, UK.ORCID 0000-0002-4213-3974
Eleanor van den HeuvelDepartment of Health Sciences, College of Health, Medicine and Life Sciences, Brunel University London, London, UK.ORCID 0000-0003-3603-2576
Claire PentecostUniversity of Exeter Medical School, University of Exeter, Exeter, UK.ORCID 0000-0003-2048-5538
Catherine QuinnCentre for Applied Dementia Studies, Faculty of Health Studies, University of Bradford, Bradford, UK.ORCID 0000-0001-9553-853X
Catherine CharlwoodUniversity of Exeter Medical School, University of Exeter, Exeter, UK.ORCID 0000-0002-3522-8457
Linda ClareUniversity of Exeter Medical School, University of Exeter, Exeter, UK.ORCID 0000-0003-3989-5318

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

DementiaAgedBangladeshCaregiversEthnicityFemaleHumansIndiaInterviews as TopicMaleMiddle AgedMinority GroupsPakistanQualitative ResearchUnited Kingdombelongingethnicityracismresponding to dementiathe migrant lifecourseunderstanding dementia

Identifiers

PMID39152913
PMCPMC11437690

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.