Resources

Deimling, G. T. & Looman, W. J. (1993). Predictors of the use of respite services by caregivers of Alzheimer's patients: Racial and generational differences. Sociological Practice, 11(1), 158-175.

Menne, H. L., Judge, K. S., & Whitlatch, C. J. (2009). Predictors of quality of life for individuals with dementia: Implications for intervention. Dementia: The International Journal of Social Research and Practice, 8(4), 543-560. doi:10.1177/1471301209350288

Whitlatch, C. J., Feinberg, L. F., & Stevens, E. J. (1999). Predictors of institutionalization for persons with Alzheimer's disease and the impact on family caregivers. Journal of Mental Health and Aging, 5(3), 275-288.

Biegel, D. E., Bass, D. M., Schultz, R., & Morycz, R. (1993). Predictors of in-home and out-of home service use by family caregivers of Alzheimer's disease patients. Journal of Aging and Health, 5(4), 419-438. doi:10.1177/089826439300500401

Moon, H., Townsend, A. L., Dilworth-Anderson, P. & Whitlatch, C. (2016). Predictors of discrepancy between care recipients with mild-to-moderate dementia and their caregivers on perceptions of the care recipients' quality of life. American Journal of Alzheimer’s Disease and Other Dementias, 31(6), 508-515. doi:10.1177/1533317516653819