Purpose: The aims of this study were to identify the effects of caring burden and the way of coping on burnout in caregivers of cancer patients. Methods: One-hundred and forty family caregivers of cancer patients who visited the cancer center at one tertiary hospital in metropolitan city B were included. The data collection was conducted from August 1st to October 1st, 2018, using a structured, self-reported questionnaire. The collected data were analyzed using descriptive statistics, t-test, one-way ANOVA, Pearson correlation coefficients, and multiple regression. Results: In the multiple regression analysis, the subject’s gender (β=.12, p=.028) and caring burden (β=.74, p<.001) had a significant effect on burnout. The explanatory power of the subject’s gender, education level, religion, caring time, number of family caregivers, monthly income, economic burden, expectation for treatment, caring burden, the way of aggressive coping, and the way of passive coping with burnout was 63.8% (F=23.28, p<.001). Conclusion: Reducing the caring burden in family caregivers of cancer patients will ultimately contribute to reducing burnout, thereby contributing to an improvement in the psychological well-being and quality of life of family members, as well as positively contributing to the recovery of patients.
목차
Abstract 서론 1. 연구의 필요성 2. 연구목적 연구방법 1. 연구설계 2. 연구대상 3. 연구도구 4. 자료수집 5. 자료분석 연구결과 1. 대상자의 일반적 특성 2. 대상자의 돌봄부담감, 대처방식, 소진의 정도 3. 대상자의 일반적 특성에 따른 소진의 차이 4. 대상자의 돌봄부담감, 대처방식, 소진의 상관관계 5. 대상자의 돌봄부담감과 대처방식이 소진에 미치는 영향 논의 결론 및 제언 REFERENCES
키워드
돌봄제공자돌봄부담감대처방식소진CaregiverBurnoutCoping behaviorBurden of illness
저자
허수빈 [ Heo, Su Bin | 인제대학교 부산백병원 간호사 ]
신소영 [ Shin, So Young | 인제대학교 의과대학 간호학과 조교수 ]
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