Statistics and society: a study on the burden experienced by caregivers of patients with Alzheimer

Abstract

The cost of caring for people with Alzheimer-type diseases is enormous. Caregivers experience emotional, physical and financial stress, and their demands are central to decisions on patient institutionalization. We hereby investigate the burden experienced by caregivers of Alzheimer patients in Cyprus. We explore whether burden is related to variables such as patient psychopathology, caregiver gender, income and level of education. Moreover, we examine if there is a significant difference in the level of burden, depression, or reaction to memory and behavior problems when patients live in the community or in institutions and if the level of burden is associated with the use of different coping strategies by caregivers. Various statistical techniques are implemented for the analysis and all the conclusions are discussed. This work was partially funded by the Cyprus Research Promotion Foundation.