Culturally competent communication in Indigenous disability assessment: a qualitative study.


Journal

International journal for equity in health
ISSN: 1475-9276
Titre abrégé: Int J Equity Health
Pays: England
ID NLM: 101147692

Informations de publication

Date de publication:
01 03 2021
Historique:
received: 03 11 2020
accepted: 07 02 2021
entrez: 2 3 2021
pubmed: 3 3 2021
medline: 14 9 2021
Statut: epublish

Résumé

Indigenous people tend to exhibit a higher burden of disability than their non-Indigenous counterparts, and are often underserved by disability services. Engaging appropriately with Indigenous communities, families and individuals in the initial stages of disability assessment and planning is crucial in order to build trust and understanding of disability service models and ensure that Indigenous people receive support that is tailored to their needs and cultural realities. This article aims to identify key elements of culturally competent communication in Indigenous disability assessment and planning, and provide recommendations for strengthening capacity in this area. This qualitative research was designed to involve Aboriginal and Torres Strait Islander people at all stages and to reflect the views of Aboriginal and Torres Strait Islander researchers, people and families affected by disability and the community-controlled health sector. Semi-structured individual interviews were undertaken with staff implementing the National Disability Insurance Scheme (NDIS) (n = 4), NDIS participants (n = 24), disability support providers and organisational partners (n = 19) and Community Connectors (n = 8) in Queensland and the Northern Territory of Australia. Key themes derived from thematic analysis included appropriate and adequate engagement of individuals with disability and their families, the role of trusted relationships, and culturally safe and appropriate communication during planning meetings. Overall, the research findings highlight that a low level of cultural competence in the initial stages of the disability assessment and planning process exacerbated participant confusion and distrust towards assessment staff and the NDIS. Given difficulties in communication, participant understanding of the NDIS was generally limited. The necessity of culturally safe and appropriate use of interpreters was stressed, as was the role of trusted individuals, including existing service providers, Community Connectors and family members in providing a solid base for participant understanding of the NDIS. Cultural competence in disability assessment and planning can be strengthened through multi-level engagement with the Aboriginal community-controlled sector and community leaders. Implementing mechanisms to enable the involvement of families, trusted service providers and Community Connectors can support a more meaningful understanding of individuals' needs within their cultural context and in relation to their cultural roles.

Sections du résumé

BACKGROUND
Indigenous people tend to exhibit a higher burden of disability than their non-Indigenous counterparts, and are often underserved by disability services. Engaging appropriately with Indigenous communities, families and individuals in the initial stages of disability assessment and planning is crucial in order to build trust and understanding of disability service models and ensure that Indigenous people receive support that is tailored to their needs and cultural realities. This article aims to identify key elements of culturally competent communication in Indigenous disability assessment and planning, and provide recommendations for strengthening capacity in this area.
METHODS
This qualitative research was designed to involve Aboriginal and Torres Strait Islander people at all stages and to reflect the views of Aboriginal and Torres Strait Islander researchers, people and families affected by disability and the community-controlled health sector. Semi-structured individual interviews were undertaken with staff implementing the National Disability Insurance Scheme (NDIS) (n = 4), NDIS participants (n = 24), disability support providers and organisational partners (n = 19) and Community Connectors (n = 8) in Queensland and the Northern Territory of Australia. Key themes derived from thematic analysis included appropriate and adequate engagement of individuals with disability and their families, the role of trusted relationships, and culturally safe and appropriate communication during planning meetings.
RESULTS
Overall, the research findings highlight that a low level of cultural competence in the initial stages of the disability assessment and planning process exacerbated participant confusion and distrust towards assessment staff and the NDIS. Given difficulties in communication, participant understanding of the NDIS was generally limited. The necessity of culturally safe and appropriate use of interpreters was stressed, as was the role of trusted individuals, including existing service providers, Community Connectors and family members in providing a solid base for participant understanding of the NDIS.
CONCLUSIONS
Cultural competence in disability assessment and planning can be strengthened through multi-level engagement with the Aboriginal community-controlled sector and community leaders. Implementing mechanisms to enable the involvement of families, trusted service providers and Community Connectors can support a more meaningful understanding of individuals' needs within their cultural context and in relation to their cultural roles.

Identifiants

pubmed: 33648504
doi: 10.1186/s12939-021-01402-9
pii: 10.1186/s12939-021-01402-9
pmc: PMC7923453
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

68

Références

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pubmed: 31068230
Aust N Z J Public Health. 2020 Aug;44(4):271-278
pubmed: 32510736
Aust Health Rev. 2018 Apr;42(2):227-229
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Health Soc Care Community. 2006 Mar;14(2):125-35
pubmed: 16460362

Auteurs

Angeline Ferdinand (A)

Centre for Health Policy, School of Population and Global Health, University of Melbourne, Parkville, VIC, 3011, Australia. a.ferdinand@unimelb.edu.au.

Libby Massey (L)

MJD Foundation, Nightcliff, NT, 0814, Australia.
James Cook University, Cairns,, QLD, 4870, Australia.

Jennifer Cullen (J)

Synapse, Level 1/262 Montague Road, West End, QLD, 4101, Australia.

Jeromey Temple (J)

Centre for Health Policy, School of Population and Global Health, University of Melbourne, Parkville, VIC, 3011, Australia.

Kristy Meiselbach (K)

Centre for Health Policy, School of Population and Global Health, University of Melbourne, Parkville, VIC, 3011, Australia.

Yin Paradies (Y)

Alfred Deakin Institute for Citizenship and Globalisation, Deakin University, 221 Burwood Highway, Burwood, VIC, 3125, Australia.

Gareth Baynam (G)

Western Australian Register of Developmental Anomalies and Genetic Services of Western Australia, King Edward Memorial Hospital, 374 Bagot Rd, Subiaco, WA, 6008, Australia.
Telethon Kids Institute and the Faculty of Health and Medical Science, Division of Paediatrics, University of Western Australia, Monash Avenue, Nedlands, WA, 6009, Australia.

Ravi Savarirayan (R)

Victorian Clinical Genetics Services, The Royal Children's Hospital, 50 Flemington Rd, Parkville, VIC, 3052, Australia.
University of Melbourne, Parkville, VIC, 3052, Australia.

Margaret Kelaher (M)

Centre for Health Policy, School of Population and Global Health, University of Melbourne, Parkville, VIC, 3011, Australia.

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Classifications MeSH