Research Article
Why caregivers of people with dementia and memory loss don't use services
Henry Brodaty,
Cathy Thomson,
Claire Thompson,
Michael Fine,
Corresponding Author
Henry Brodaty
School of Psychiatry, University of New South Wales, Australia
Academic Department for Old Age Psychiatry, Prince of Wales Hospital, Sydney, Australia
Academic Department for Old Age Psychiatry Euroa Centre, Prince of Wales Hospital, Avoca St, Randwick, Sydney NSW 2031, Australia.Search for more papers by this authorCathy Thomson
Social Policy Research Centre, University of New South Wales, Australia
Search for more papers by this authorClaire Thompson
Academic Department for Old Age Psychiatry, Prince of Wales Hospital, Sydney, Australia
Search for more papers by this authorMichael Fine
Department of Sociology, Macquarie University, Australia
Search for more papers by this authorHenry Brodaty,
Cathy Thomson,
Claire Thompson,
Michael Fine,
Corresponding Author
Henry Brodaty
School of Psychiatry, University of New South Wales, Australia
Academic Department for Old Age Psychiatry, Prince of Wales Hospital, Sydney, Australia
Academic Department for Old Age Psychiatry Euroa Centre, Prince of Wales Hospital, Avoca St, Randwick, Sydney NSW 2031, Australia.Search for more papers by this authorCathy Thomson
Social Policy Research Centre, University of New South Wales, Australia
Search for more papers by this authorClaire Thompson
Academic Department for Old Age Psychiatry, Prince of Wales Hospital, Sydney, Australia
Search for more papers by this authorMichael Fine
Department of Sociology, Macquarie University, Australia
Search for more papers by this authorAbstract
Objectives
To develop a typography of the characteristics of caregivers of community dwelling people with dementia or memory loss who do not use services and empirically investigate the reasons for service non-use.
Method
The findings of a literature review were used to develop a typography of caregivers' non-use of services. This typography was applied to a sample of community-based caregivers.
Results
One in three caregivers were using no services and one in four only one service. Despite considerable proportions reporting low levels of life satisfaction and high levels of overload and resentment the main reasons caregivers gave for not using services were that they did not consider they needed the services. Other reasons for service non-use included care recipient reluctance to use services, lack of knowledge of services or being in the process of applying for services. Service availability or affordability were not identified as major impediments to service use. Presence of a physical disability and contact with a social worker were associated with service use.
Conclusions
Caregivers of people with dementia incur significant strain and have substantial need for a variety of services. Nevertheless many caregivers were not using support services, mainly because of perceived lack of need or lack of awareness. Better public promotion of services, destigmatising dementia and encouraging referrals from health professionals could help overcome the barriers to service use. Copyright © 2005 John Wiley & Sons, Ltd.
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