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Larkin, John P.; Hopcroft, Barbara Most – Health & Social Work, 1993
Obtained data on family caregiver stress from 23 family caregivers before, during, and following respite. Findings suggest that stress was moderated by in-hospital respite program for patients with Alzheimer's disease. Although short-term benefits may be realized for caregivers, in-hospital Alzheimer's respite care may present particular risk for…
Descriptors: Alzheimers Disease, Family Caregivers, Hospitals, Patients
Peer reviewed Peer reviewed
Ehrlich, Phyllis; White, Judith – Gerontologist, 1991
Describes Time Off Promotes Strength (TOPS), program for caregivers of Alzheimer's victims which provides in-home and day program services. Explains that, through application of service/training model adapted from Global Deterioration Scale, TOPS maintains high quality of services with limited but highly trained professional staff. (Author/NB)
Descriptors: Alzheimers Disease, Coping, Family Caregivers, Individual Needs
Pietrukowicz, Mary; Johnson, Mitzi M. S. – 1989
Studies consistently have found that caregivers who use respite care are satisfied with and appreciate such care. However, preliminary evaluations of the effect of respite care on caregiver burden have had mixed, limited, and in some cases null empirical findings of program effectiveness. This study explored the relationship between caregiver…
Descriptors: Alzheimers Disease, Chronic Illness, Disabilities, Family Caregivers
Peer reviewed Peer reviewed
Lawton, M. Powell; And Others – Gerontologist, 1989
Conducted baseline interviews with 642 caregivers of aged Alzheimer's disease patients, then assigned one-half to formal respite care. Over 12 months, families with respite care maintained Alzheimer's patient significantly longer in community than did caregivers without respite. Respite care was ineffective for caregiver burden and mental health,…
Descriptors: Alzheimers Disease, Chronic Illness, Family Caregivers, Mental Health
Peer reviewed Peer reviewed
Berry, Greta L.; And Others – Gerontologist, 1991
Examined use of time among female caregivers of dementia patients who used home care (n=20) and day care (n=20) respite services. Assessment of caregiver activity during respite and nonrespite days revealed significant program differences in amount of caregiving time and overall differences in amount of noncaregiving time. Use of respite time was…
Descriptors: Adult Day Care, Alzheimers Disease, Daughters, Family Caregivers