Method: A descriptive design was used. One hundred sixteen women family caregivers of persons diagnosed with AD participated in the study. Family caregivers were interviewed face to face and responded to a questionnaire that includes demographic information, perceived health, time restriction, perceived stressed, activities, and care-recipient’s memory-related behavior problems. Descriptive statistical analyses, bivariate, and multiple regression analyzes were performed.
Results: The results showed that 41% of the variance on depression was explained by caregiver’s perceived health, stress, time restriction, and presence of disruptive behavior. Twenty –five percent of the family caregivers scored over 9 in the 10-item CESD indicating depression but only one sought mental health service. Reasons for not seeking mental health services are: stigma in seeing a mental health provider, belief that depression will just go away, lack of knowledge regarding available mental health provider, no insurance, and no time to see a physician.
Conclusions: Formal caregivers must act together to provide accessible and affordable programs and support services to screen caregiver’s health and depression, provide relief or respite, and teach caregivers stress management and how to deal with behavior problems.