The role of caregiver burden in the familial functioning, social support, and quality of family life of family caregivers of elders with dementia

Author:

Kimura Hiromi1,Nishio Midori2,Kukihara Hiromko1,Koga Kayoko1,Inoue Yuriko1

Affiliation:

1. School of Nursing, Fukuoka University of Medicine, Japan

2. Japanese Red Cross Kyushu International College of Nursing, Japan

Publisher

Japanese Association of Rural Medicine

Reference41 articles.

1. 1. Miyajima T . General outline for dementia policy. Cognition and Dementia 2012 the report by the Ministry of Health. Labour and Welfare 2013; 12: 100–104.

2. 2. Karasawa H , Yasuma Y , Utagawa M , et al. A study on reliability and validity of speed interview sheet/differential diagnosis table for memory loss. Community Med 2014; 28: 504–512.

3. 3. Sakurai S , Kono Y , Hirai M . Characteristics of stress management methods in family caregivers living with persons requiring care. The Journal of Japan Academy of Home Care 2015; 19: 68–73.

4. 4. Terao S . The characteristic of caregivers who continue nursing care for the elderly consideration with fact-finding survey and interview survey. The study of social welfare 2010; 5: 19–27.

5. 5. Yoshizawa M , Sugisawa H . The effect on a sense of care burden by a level of family caregiver’s understanding for dementia. Journal of Gerontological Research 2012; 2: 43–56.

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