Resources

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

Whitlatch, C. J. (2006). Older consumers and decision making: A look at family caregivers and care receivers. In S. Kunkel & V. Wellin (Eds.), Consumer voice and choice in long-term care (pp. 3-19). New York, NY: Springer.

Bradford, A., Upchurch, C., Bass, D., Judge, K., Snow, A. L., Wilson, N., & Kunik, M. E. (2011). Knowledge of documented dementia diagnosis and treatment in veterans and their caregivers. American Journal of Alzheimer's Disease and Other Dementias, 26(2), 127-133. doi:10.1177/1533317510394648