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Bass, D. M. (1985). The hospice ideology and success of hospice care. Research on Aging, 7(3), 307-327. doi:10.1177/0164027585007003001

Menne, H. L., Bass, D. M., Johnson, J. D., Primetica, B., Kearney, K. R., Bollin, S., Molea, M. J., & Teri, L. (2014). Statewide implementation of "Reducing Disability of Alzheimer's Disease”: Impact on family caregiver outcomes. Journal of Gerontological Social Work, 57(6/7), 626-639. doi:10.1080/01634372.2013.870276

Rose , M., Ejaz, F. K., Noelker, L. S., Castora-Binkley, M. (2010). Recent findings on home- and community-based services across the states. Public Policy and Aging Report, 20(1), 10-15. doi:10.1093/ppar/20.1.10

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