| 英文摘要 |
Family members of patients receiving Severe Home Health Care, through their caregiving experiences or witnessing the patient's progression from health to complete disability, may be prompted to deeply reflect on the nature and meaning of life. This reflection could lead them to pay closer attention to the Patients’Right to Autonomy Act and the potential for pre-signing Advance Directives. The aim of this study is to explore the family members' knowledge, attitudes, and behavioral intentions regarding Advance Directives for patients receiving Severe Home Health Care, as well as to examine the relationships between these factors. Additionally, the study analyzes how the demographic characteristics of family members influence their knowledge, attitudes, and behavioral intentions. Using a questionnaire survey, purposive sampling was conducted among close relatives of patients receiving Severe Home Health Care, affiliated with the home care departments of a medical center and a regional hospital in central Taiwan. Data collection took place from June to October 2023, resulting in 199 valid responses. Statistical analysis was performed using SPSS 20.0, with descriptive statistics, the Mann-Whitney U test, Kruskal-Wallis test, and Spearman's rank correlation method. Key findings: (1) Over 80% of respondents understood the conditions under which Advance Directives become effective but lacked knowledge of the legal procedures involved. (2) Women, non-cohabitating family members, retirees, and those who perceived themselves to be in good health had higher levels of knowledge about Advance Directives. (3) Respondents under the age of 50, with higher education levels, and those with very close relationships with the patient exhibited more positive attitudes. (4) Family members of patients who had verbally expressed their end-of-life medical preferences or signed Do Not Resuscitate (DNR) orders had higher behavioral intentions regarding Advance Directives. |