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(1989)
The differential impact of burden on spouse and adult child caregivers of dementia patients
M. Ory, T. Williams, M. Emr, B. Lebowitz, P. Rabins, J. Salloway, T. Sluss-Radbaugh, E. Wolff, S. Zarit (1987)
Families, informal supports, and Alzheimerʼs disease: current research and future agendasAlzheimer Disease & Associated Disorders, 1
M. Novak, C. Guest (1989)
Caregiver Response to Alzheimer's DiseaseThe International Journal of Aging and Human Development, 28
B. Robinson (1983)
Validation of a Caregiver Strain Index.Journal of gerontology, 38 3
J. Kosberg, R. Cairl (1986)
The Cost of Care Index: a case management tool for screening informal care providers.The Gerontologist, 26 3
E. Colerick, L. George (1986)
Predictors of Institutionalization Among Caregivers of Patients With Alzheimer's DiseaseJournal of the American Geriatrics Society, 34
Age and the Life Course
Aging, Society, and the Life Course
(1983)
Caregiver stress in dementia : Clinical outcomes and family considerations
S. Poulshock, G. Deimling (1984)
Families caring for elders in residence: issues in the measurement of burden.Journal of gerontology, 39 2
G. Niederehe, E. Frugé (1984)
Dementia and family dynamics: clinical research issues.Journal of geriatric psychiatry, 17 1
R. Morycz (1985)
Caregiving Strain and the Desire to Institutionalize Family Members with Alzheimer's DiseaseResearch on Aging, 7
R. Montgomery, J. Gonyea, N. Hooyman (1985)
Caregiving and the experience of subjective and objective burden.Family Relations, 34
L. George, L. Gwyther (1986)
Caregiver well-being: a multidimensional examination of family caregivers of demented adults.The Gerontologist, 26 3
(1982)
Measuring burden and support in families with Alzheimer ' s disease elders
(1985)
Social correlates of caregiver burden
S. Zarit, K. Reever, J. Bach-Peterson (1980)
Relatives of the impaired elderly: correlates of feelings of burden.The Gerontologist, 20 6
(1987)
Development and preliminary validation of a caregiver burden inventory
C. Guest (1986)
An investigation of the dimensions of burden in family caregivers of Alzheimer's disease patients.
Abstract Multidimensional measures of caregiver burden give a sensitive reading of caregivers' feelings and a sophisticated picture of caregivers' responses to the demands of care. This paper reports on the development of a 24-item, five-subscale Caregiver Burden Inventory (CBI) and demonstrates its use as a diagnostic tool for professional caregivers. It concludes with a discussion of several ways that professional caregivers can use this multidimensional measure of caregiver burden. Alzheimer's disease, Family support, Assessment This content is only available as a PDF. Author notes 1 The first author gratefully acknowledges support in this research by a Leave Fellowship from the Social Sciences and Humanities Research Council of Canada. The first author also acknowledges the support of the University of Winnipeg, where the author worked while conducting this study. © 1989 The Gerontological Society of America
The Gerontologist – Oxford University Press
Published: Dec 1, 1989
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