英文摘要 |
In Taiwan, there are about 90% of the intellectual disabled living at home, and most of their caregivers are their parents. As the intellectual disability people get older, their parents are getting older, and the aging parents are gradually unable to take care of their children. In the past few decades, there had been few studies focused on caregivers, and most of these researches are based on qualitative research. Furthermore, empirical data on the relationship between formal social support, informal social support and caregiving burden in Taiwan are insufficient. Thus, this study used survey research and adopted the Supplemental Model to examine the effect between different support combinations and whether they can reduce the caregiving burden. This study utilized purposive sampling, and the data were gathered from the intellectual disability service agencies in northern Taiwan (total 7 institutions). Data were compiled through structured questionnaires which were interviewed by social workers. Participants were the caregivers of intellectual disability children, and a total of 74 questionnaires was received. Analysis of variance (ANOVA) was used to test the research hypothesis, and multiple regression analysis was utilized to explore the factors of caregiving burden. The results showed that the caregivers had a low level of social support and a high level of caregiving burden. In addition, the “high level of informal support” group had the lowest caregiving burden, which is consistent with the hypothesis of the Supplemental Model that the informal care system is the primary one, and the formal system is used to supplement the informal system. The study also demonstrated a significant negative correlation between “information support” and “caregiving burden,” as well as “emotional support” and “caregiving burden.” By using regression analysis, it was found that “health status” and “emotional support” can significantly predict the caregiving burden, it indicated that the poorer the caregivers' health, the lower the emotional support, and the higher the caregiving burden. According to these findings, we suggest that service providers and policy makers should improve the care support system on the basis of “mainly rely on informal system supplemented by formal system” and should pay more attention to the needs of the caregivers. In addition, service providers and policy makers should understand the importance of emotional support services. Furthermore, the instrumental support services need to be reinforced in order to reduce the caregiving burden. |