英文摘要 |
The major purpose of this study was to explore the changes of disease cognition, social support, and burden of caregivers of stroke patients before and after receiving health education. The design was longitudinal and used purposive sampling. One hundred forty-three (143) main caregivers of stroke patients were recruited at a neuro-medical ward of a medical center in northern Taiwan. A structured questionnaire and assessment tool was used to collected data at five time intervals: pre-education, pre-discharge, and the first month, the sixth month, and the first year post-discharge. Multivariate and univariate repeated measures were used to analyze the data. The results were as follows. First, the main caregivers' knowledge about stroke improved significantly after health education, but declined one year post-discharge. However, the knowledge score after one year was still higher than at pre-education. Second, the function of emotional and informational social support improved steadily after health education. Finally, when compared with the pre-education time, the psychological burden declined significantly at the first month, the sixth month, and the first year post discharge. Results suggested that cooperation on discharge planning between acute hospitals and community care agencies is necessary to improve caregivers' knowledge of stroke and social supports. Moreover, instrumental support for health education needs to be implemented to decrease the burden of caregivers. |