Background: The burden produced by caring for relatives with dementia is an
increasing problem in the United States and Taiwan, necessitating a better
understanding of the interrelationships of the factors that influence burd
en.
Objectives: To test a theoretical model specifying how the demands of care,
filial obligation, caregiving self-efficacy, coping strategies, and caregi
ving involvement affect caregiver burden.
Method: A descriptive cross-sectional design with a convenience sample (n =
150) from outpatient clinics of three,hospitals in Taiwan was used. The Ca
regiver Burden Inventory and the Cost of Care index assessed caregiver burd
en. The antecedents of burden were assessed by the Physical Self; Maintenan
ce Scale, Instrumental Activities of Daily Living, the Mini-Mental State Ex
amination, the Revised Memory and Behavior Problem Checklist, the Montgomer
y obligation subscale, Cicirelli's obligation scale, the Caregiving Self-ef
ficacy Scale, the Caregiving Involvement Scale. and the Ways of Coping Ques
tionnaire.
Results: The original model did not fit the data well but minor respecifica
tions produced a good model as evidenced by a X-2/df ratio of 2.1, a goodne
ss-of-fit index of .89, and a comparative fit index of .93. Demands of care
on, the caregiver and filial obligation had direct positive effects on car
egiving involvement. Caregiving involvement and emotion-focused coping had
direct positive effects on caregiving burden. Filial obligation, caregiving
self-efficacy, and problem-focused coping had direct negative effects on c
aregiving burden. Six of the seven original hypothesized structural relatio
nships were-confirmed in the final model.
Conclusions: The Burden Model tested in this study corroborates findings fr
om other burden studies and extends our knowledge of caregiver burden. Fili
al obligation, self-efficacy, demands of care, involvement in care,and copi
ng were shown to predict burden in this sample of Taiwanese caregivers. Fut
ure study is needed to evaluate interventions designed for family caregiver
s of persons with dementia, Especially needed is research in the area of co
unseling and mental health services to assist caregivers in dealing with ma
nifestations of burden.