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A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities

BACKGROUND: People with dementia and their family carers need to be able to access formal services in the community to help maintain their wellbeing and independence. While knowing about and navigating one’s way through service systems is difficult for most people, it is particularly difficult for p...

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Autores principales: Shanley, Christopher, Boughtwood, Desiree, Adams, Jon, Santalucia, Yvonne, Kyriazopoulos, Helena, Pond, Dimity, Rowland, Jeffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523018/
https://www.ncbi.nlm.nih.gov/pubmed/23043332
http://dx.doi.org/10.1186/1472-6963-12-354
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author Shanley, Christopher
Boughtwood, Desiree
Adams, Jon
Santalucia, Yvonne
Kyriazopoulos, Helena
Pond, Dimity
Rowland, Jeffrey
author_facet Shanley, Christopher
Boughtwood, Desiree
Adams, Jon
Santalucia, Yvonne
Kyriazopoulos, Helena
Pond, Dimity
Rowland, Jeffrey
author_sort Shanley, Christopher
collection PubMed
description BACKGROUND: People with dementia and their family carers need to be able to access formal services in the community to help maintain their wellbeing and independence. While knowing about and navigating one’s way through service systems is difficult for most people, it is particularly difficult for people from culturally and linguistically diverse (CALD) communities. This study addresses a lack of literature on the use of formal services for dementia by people from CALD backgrounds by examining the experiences and perceptions of dementia caregiving within four CALD communities – Italian, Chinese, Spanish and Arabic-speaking – in south western Sydney, Australia. METHODS: The study used a qualitative design and the methods included focus groups with family carers and one-to-one interviews with bilingual/bicultural community workers, bilingual general practitioners and geriatricians. A total of 121 family carers participated in 15 focus groups and interviews were held with 60 health professionals. All fieldwork was audiotaped, transcribed and subjected to thematic analysis. RESULTS: People from CALD communities are often unfamiliar with the concept of formal services and there may be strong cultural norms about maintaining care within the family, rather than relying on external services. CALD communities often have limited knowledge of services. There is a preference for services that will allow families to keep their relative at home, for safety as well as cultural reasons, and they are particularly reluctant to use residential care. While there is a preference for ethno-specific or multicultural services, mainstream services also need to ensure they are more flexible in providing culturally appropriate care. Positive outcomes occur when ethno-specific services work in partnership with mainstream programs. Dementia service providers need to develop a trusting relationship with their local CALD communities and promote their services in a way that is understandable and culturally acceptable to members of these communities. CONCLUSIONS: While members of CALD communities may have difficulties accessing formal services, they will use them if they are culturally and linguistically appropriate and can meet their needs. There are a number of ways to improve service provision to CALD communities and the responsibility for this needs to be shared by a range of stakeholders.
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spelling pubmed-35230182012-12-16 A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities Shanley, Christopher Boughtwood, Desiree Adams, Jon Santalucia, Yvonne Kyriazopoulos, Helena Pond, Dimity Rowland, Jeffrey BMC Health Serv Res Research Article BACKGROUND: People with dementia and their family carers need to be able to access formal services in the community to help maintain their wellbeing and independence. While knowing about and navigating one’s way through service systems is difficult for most people, it is particularly difficult for people from culturally and linguistically diverse (CALD) communities. This study addresses a lack of literature on the use of formal services for dementia by people from CALD backgrounds by examining the experiences and perceptions of dementia caregiving within four CALD communities – Italian, Chinese, Spanish and Arabic-speaking – in south western Sydney, Australia. METHODS: The study used a qualitative design and the methods included focus groups with family carers and one-to-one interviews with bilingual/bicultural community workers, bilingual general practitioners and geriatricians. A total of 121 family carers participated in 15 focus groups and interviews were held with 60 health professionals. All fieldwork was audiotaped, transcribed and subjected to thematic analysis. RESULTS: People from CALD communities are often unfamiliar with the concept of formal services and there may be strong cultural norms about maintaining care within the family, rather than relying on external services. CALD communities often have limited knowledge of services. There is a preference for services that will allow families to keep their relative at home, for safety as well as cultural reasons, and they are particularly reluctant to use residential care. While there is a preference for ethno-specific or multicultural services, mainstream services also need to ensure they are more flexible in providing culturally appropriate care. Positive outcomes occur when ethno-specific services work in partnership with mainstream programs. Dementia service providers need to develop a trusting relationship with their local CALD communities and promote their services in a way that is understandable and culturally acceptable to members of these communities. CONCLUSIONS: While members of CALD communities may have difficulties accessing formal services, they will use them if they are culturally and linguistically appropriate and can meet their needs. There are a number of ways to improve service provision to CALD communities and the responsibility for this needs to be shared by a range of stakeholders. BioMed Central 2012-10-09 /pmc/articles/PMC3523018/ /pubmed/23043332 http://dx.doi.org/10.1186/1472-6963-12-354 Text en Copyright ©2012 Shanley et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shanley, Christopher
Boughtwood, Desiree
Adams, Jon
Santalucia, Yvonne
Kyriazopoulos, Helena
Pond, Dimity
Rowland, Jeffrey
A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title_full A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title_fullStr A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title_full_unstemmed A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title_short A qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (CALD) communities
title_sort qualitative study into the use of formal services for dementia by carers from culturally and linguistically diverse (cald) communities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523018/
https://www.ncbi.nlm.nih.gov/pubmed/23043332
http://dx.doi.org/10.1186/1472-6963-12-354
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