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Support Needs of Elderly Caregivers of Persons with Dementia*

Published online by Cambridge University Press:  29 November 2010

Angela Colantonio
Affiliation:
University of Toronto
Carole Cohen
Affiliation:
Sunnybrook Health Science Centre
Sue Corlett
Affiliation:
University of Toronto

Abstract

The aim of this paper was (1) to document the extent to which elderly caregivers of persons with dementia engage in self-help/mutual aid activities such as groups and telephone support and (2) to document the extent to which non-users want to participate in this form of support. Caregivers aged 60 years of age and older were recruited from the Alzheimer's Society of Metropolitan Toronto Wandering Persons Registry. Data from telephone interviews (n = 84) from this multicultural sample showed that 21 per cent of subjects used support groups and 26 per cent of non attenders wanted to be part of a support group. Only 8 per cent of subjects utilized telephone support services yet 57 per cent of non-users wanted to use this service. We also report on other means of support such as use of computer networks and newsletters. The implications of this research for seniors will be discussed in light of these identified needs and barriers to participation.

Résumé

L'objet de cette étude était (1) de déterminer jusqu'à quel point les dispensateurs de soins âgés s'occupant de personnes atteintes de démence participent à des activités de soutien individuel (assistance téléphonique) ou de groupe, et (2) de déterminer jusqu'à quel point les non-participants souhaitent utiliser cette forme de soutien. On a recruté les dispensateurs de soins âgés de 60 ans et plus à partir du registre des personnes errantes de la Société Alzheimer du Toronto métropolitain. Les données provenant des entrevues téléphoniques (n = 84) parmi cet échantillonnage multiculturel ont indiqué que 21 pour cent des sujets ont utilisé les groupes de soutien et que 26 pour cent des non-participants souhaitaient faire partie d'un groupe de soutien. Seulement 8 pour cent des sujets ont utilisé les services d'assistance téléphonique même si 57 pour cent des non-utilisateurs voulaient avoir recours à ce service. Nous faisons également état d'autres moyens de soutien tels que les réseaux informatiques et les bulletins d'information. Les implications de cette étude pour les personnes âgées seront discutées à la lumière de ces besoins identifiés et des barrières à la participation.

Type
Articles
Copyright
Copyright © Canadian Association on Gerontology 1998

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References

Brennan, P.F., Moore, S.M., & Smyth, K.A. (1992). Alzheimer's disease caregivers uses of a computer network. Western Journal of Nursing Research, 14(5), 662673.CrossRefGoogle ScholarPubMed
Canada. Department of Health. (1994). Strategies for population health: Investing in the health of Canadians. Ottawa, ON: Minister of Supply and Services Canada.Google Scholar
Canadian Study of Health and Aging Working Group. (1994). Patterns of caring for people with dementia in Canada. Canadian Journal on Aging, 13(4), 470487.CrossRefGoogle Scholar
Chiverton, P., & Caine, E. (1989). Education to assist spouses in coping with Alzheimer's disease: a controlled trial. Journal of the American Geriatric Society, 37, 593–487.CrossRefGoogle Scholar
Davies, H., Priddy, J.M., & Tinklenberg, J.R. (1986). Support groups for male caregivers of Alzheimer's patients. Clinical Gerontologist, 5(3/4), 385395.CrossRefGoogle Scholar
Farran, C.J., & Keane-Hagerty, E. (1994). Interventions for caregivers or persons with dementia: educational support groups and Alzheimer's Association support groups. Applied Nursing Research, 7(3), 112117.CrossRefGoogle ScholarPubMed
Fillenbaum, G.G. (1978). Validity and reliability of the multidimensional Functional Assessment Questionnaire. Multidimensional Functional Assessment: The OARS Methodology, Duke University Center for the Study of Aging and Human Development. Durham, NC: Duke University.Google Scholar
Fried, L.P., Borhani, N.O., Enright, P., Furberg, C.D., Gardin, J.M., Kronmal, R.A., Kuller, L.H., Manolio, T.A., Mittelmark, M.B., Newman, A., et al. (1991). The Cardiovascular Health Study: design and rationale. Annals of Epidemiology, 1(3), 263276.CrossRefGoogle ScholarPubMed
Gonyea, J.G. (1989). Alzheimer's disease support groups: and analysis of then-structure, format and perceived benefits. Social Work in Health Care, 14(1), 6172.CrossRefGoogle Scholar
Goodman, C.C., & Pynoos, J. (1990). A model telephone information and support program for caregivers of Alzheimer's patients. The Gerontologist, 30(3), 399404.CrossRefGoogle Scholar
Gottlieb, B.H., & Peters, L. (1991). A national demographic portrait of mutual aid group participants in Canada. American Journal of Community Psychology, 19(5), 651666.CrossRefGoogle Scholar
Haley, W.E. (1989). Group intervention for dementia family caregivers: a longitudinal perspective. The Gerontologist, 29(4), 478480.CrossRefGoogle ScholarPubMed
Hamilton, N., & Bhatti, T. (1996). Population health promotion: An integrated model of population health and health promotion. Ottawa: Health Promotion Development Division.Google Scholar
Kane, R.A., & Kane, R.L. (1987). Long-term care: Principles, programs, and policies. New York: Springer Publishing Co.Google Scholar
Knight, B.G., Lutsky, S.M., & Macofsky-Urban, F. (1993). A meta-analytic review of interventions for caregiver distress: recommendations for future research. The Gerontologist, 33(2), 240248.CrossRefGoogle ScholarPubMed
Lavoie, F., & Stewart, M. (1995). Mutual-aid groups and support groups: The Canadian context. Canadian Journal of Mental Health, 14(2), 512.Google Scholar
Lavoie, F., Stewart, M., & Landry, S. (1996). Barriers to the use of mutual aid /self-help groups by Canadian senior citizens. Poster presentation, XXVI International Congress of Psychology, Montreal, Quebec.Google Scholar
Lovett, S., & Gallagher, D. (1988). Psychoeducational interventions for family caregivers: preliminary efficacy data. Behaviour Therapy, 19, 321330.CrossRefGoogle Scholar
Radloff, L.S. (1977). The CES-D Scale: a self-report depression scale for research in the general population. Journal of Applied Psychological Measurement, 1, 385401.CrossRefGoogle Scholar
Romeder, J.M. (1993). Of surveys and definitions of self help and mutual aid. In Self-Help /Mutual Aid for Seniors: Research Challenges. Report of the discussion session at the Canadian Association of Gerontology. Ottawa: Self Help Canada.Google Scholar
Self-Help Resource Centre of Greater Toronto. (1996). Directory of Self-Help /Mutual Aid Groups in Greater Toronto. Toronto.Google Scholar
Shultz, R., O'Brien, A.T., Bookwalla, J., & Fleissner, K. (1995). Psychiatric and physical morbidity effects of dementia caregiving: prevalence, correlates and causes. The Gerontologist, 35, 771791.Google Scholar
Shultz, R., Visintainer, P., & Williamson, G.M. (1990). Psychiatric and physical morbidity effects of caregiving. Journal of Gerontology: Psychological Sciences, 45(5), 181191.Google Scholar
Stewart, M., & Tilden, V. (1995). The contribution of nursing science to social support. International Journal of Nursing Studies, 32(6), 535544.CrossRefGoogle Scholar
Toseland, R.W., Rossiter, C.M., & Labreque, M.S. (1989). The effectiveness of peer-led and professionally led groups to support family caregivers. The Gerontologist, 29(4), 465471.CrossRefGoogle ScholarPubMed
Walker, A. (1995). The future of long-term care in Canada: A British perspective. Canadian Journal on Aging, 14(2), 437446.CrossRefGoogle Scholar
Wister, A. (1995). The relationship between self-help group participation and other health behaviours among older adults. Canadian Journal of Mental Health, 14(2), 2337.Google Scholar