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허수빈 ( Heo Su-Bin ) - 인제대학교 부산백병원
신소영 ( Shin So-Young ) - 인제대학교 의과대학 간호학과
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Abstract
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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.
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KeyWords
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돌봄제공자, 돌봄부담감, 대처방식, 소진
Caregiver, Burnout, Coping behavior, Burden of illness
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원문 및 링크아웃 정보
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등재저널 정보
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