• 한국가족복지학
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• 제53호
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• pp.235-263
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• 2016

본 연구는 치매환자 자녀의 부양부담이 배우자폭력에 미치는 영향을 파악하고 우울의 매개효과를 검증하여 사회복지적 개입방안을 찾고자 한다. 이를 위하여 서울, 경기, 부산의 각 지역 데이케어센터 및 요양기관의 치매환자와 가족을 대상으로 조사를 실시하였다. 전체 응답자 중 기혼인 치매환자의 자녀 223명의 자료를 최종 분석에 활용하였고, 빈도분석, 평균비교 및 상관관계분석 그리고 회귀분석을 실시하였다. 최종적으로 우울의 매개효과의 유의성을 검증하기 위하여 부트스트래핑(bootstrapping)을 실시하였다. 연구결과, 조사대상자의 37.6%, 즉 3명 중 1명 이상의 치매환자 자녀가 배우자에게 지난 1년간 적어도 한차례 이상 정서적 폭력이나 신체적 폭력을 행사한 것으로 나타나 배우자폭력 수준이 매우 심각한 것으로 조사되었다. 또한 조사대상자의 우울 평균은 1.00으로 일반인(M=0.73)보다 높은 수준이었으며, 여성이 남성보다 부양부담이 더 많은 것으로 나타났다. 한편 치매환자 자녀의 부양부담은 배우자폭력에 정적인 영향을 미쳤으며, 부양부담과 배우자폭력의 관계에서 매개변수인 우울은 완전매개효과가 있는 것으로 확인되었다. 이러한 연구결과를 바탕으로 부양부담, 우울을 줄이고 배우자폭력을 예방하기 위한 정책적 실천적 개입 방안을 제시하였다.

• 한국노년학
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• 제29권4호
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• pp.1591-1609
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• 2009

본 연구는 미국의 치매노인 부양자들을 대상으로 하여 치매환자가 배우자인 경우와 부모인 경우를 분리하여 이들 두 집단의 우울증이 어떠한 차이를 보이는지 또 우울증에 영향을 미치는 요소가 어떻게 다른지를 회귀모형을 통해 분석해보았다. 분석결과에 의하면, 치매에 걸린 남편을 돌보는 아내 부양자가 치매에 걸린 부모를 돌보는 딸 부양자보다 우울증 점수가 더 높은 경향성을 보여주었다. 한편, 배우자 부양자와 딸 부양자 집단의 우울증 점수에 영향을 미치는 요소들에 어떠한 공통점과 차이점을 갖고 있는지 알아보기 위해 각각의 회귀분석을 실시한 결과는 다음과 같다. 먼저, 딸 부양자의 경우 역할부담감, 역할구속감, 그리고 문제행동이 그들의 우울증에 유의미한 영향을 주었고, 아내 부양자의 경우에는 역할부담감, 역할구속감, 문제행동, 그리고 교육수준이 우울증에 유의미한 영향을 주는 변수였으며, 마지막으로 남편 부양자에게는 오직 역할구속감과 문제행동만이 그들의 우울감에 유의미한 영향을 미치는 변수로 나타났다. 따라서 모든 부양자 집단의 우울증에 공통적으로 영향을 주는 유의미한 예측변수는 역할구속감과 문제행동이었다. 즉 부양자의 역할구속감이 클수록, 그리고 피부양자인 치매환자의 문제행동 수준이 높아질수록 부양자의 우울증 점수는 높아지는 경향성을 보였다.

• 한국가족복지학
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• 제57호
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• pp.99-124
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• 2017

본 연구는 정신질환자의 가장 기본적인 보호체계인 가족의 기능에 대한 기존연구가 정신질환의 발병 단계(초기, 만성)에 대한 고려 없이 진행된 한계를 극복하고자 발병초기 정신질환자가족과 만성 정신질환자 가족의 가족기능이 차이가 있는지, 각 그룹의 가족기능에 영향을 미치는 요인이 무엇인지에 대해 살펴보는 것을 목적으로 하였다. 부산지역 정신보건 서비스 이용 정신질환자 628명을 대상으로 분석한 결과 발병초기 정신질환자의 가족기능보다 만성 정신질환자 가족기능이 더 높게 나타났다. 발병초기 정신질환자의 경우 가족기능 괴리감이 가족기능에 영향을 미치는 요인으로 확인되었다. 반면, 만성 정신질환자의 경우 일상생활수행능력, 주보호자의 건강상태, 가족기능 괴리감, 지역사회지지가 가족기능에 영향을 미치는 요인으로확인되어 두 그룹의 영향요인이 다름을 확인할 수 있었다. 이러한 연구결과를 바탕으로 실천현장에서 고려 할 수 있는 발병초기와 만성 정신질환자의 가족기능을 향상시키기 위한 차별적방법을 제언하였다.

• 보건교육건강증진학회지
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• 제16권2호
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• pp.67-80
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• 1999

This study was designed to provide the basic data of nursing intervention for alleviation of effective adjustment of cancer patients by identifying the correlation between the spiritual well-being and family support. The subjects for this study were 69 patients who were diagnosed as cancer and were admitted to a university hospital in Pusan. Data were collected during the period between December 1, 1998 and January 20, 1999 by interviewing with questionnaires. Family support questionnaire consisted of 11 questions answerable on a 5 point Likert scale developed by Kang Hyun Suk(1985). Spiritual well-being questionnaire consisted of 20 questions answerable on a 4 point Likert scale modified by Kang Jeong Ho(1996). The data were analyzed by in descriptive statistics, Pearson correlation coefficient, t-test and ANOVA using SPSS/WIN program. The results of this study were as follows. 1. The mean score for family support in cancer patients was 49.48, which indicated that cancer patients perceived their state of family support as high level. The mean score for spiritual well-being in cancer patients was 55.87, which indicated that cancer patients perceived their state of spiritual well-being as moderate level. Among the components of spiritual well-being, the mean score for religious well-being was 26.94 and for existential well-being 28.93. From the above, the mean score for existential well-being was higher than that of religious well-being. 2. There were statistically significant differences in family support according to the types of primary caregivers(F=3.48, p=0.008). The spouse caregiver showed the highest family support among the caregivers. There were statistically significant differences in spiritual well-being according to the job(F=2.20, p=0.046) and the level of perceived health status(F=2.71, p=0.05). There were statistically significant differences in religious well-being according to the religion(F=2.42, p=0.004) and the number of family members(F=3.38, p=0.040). And there were statistically significant differences in existential well-being according to the job(F=2.48, p=0.026) and the level of perceived health status(F=2.74, p=0.048). 3. There were positive correlation between spiritual well-being and the family support(r=0.481, p=0.000), between religious well-being and family support(r=0.336, p=0.008) and existential well-being and family support(r=0.519, p=0.000).

• 성인간호학회지
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• 제23권6호
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• pp.605-614
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• 2011

Purpose: The purpose of this study was to investigate the relationship among loneliness, life satisfaction, social support and perceived health status, and further to identify factors affecting loneliness among hospitalized patients with pneumoconiosis. Methods: This study was a cross-sectional descriptive survey. A sample of 205 hospitalized patients with pneumoconiosis was recruited from August 10 to 27, 2011. The data were collected using structured questionnaire and were analyzed with SPSS/WIN 17.0 program. Results: The mean score of loneliness was very high (46.5). The levels of loneliness depended on several factors including the duration of coalworker caregiver, personality, exercise, hobbies and reported complications. The reported loneliness was significantly correlated with life satisfaction (r=-.204, p=.003). family support (r=-.220, p=.002), professional medical team support (r=-.303, p<.001) and perceived health status (r=-.175, p=.012). The influential factors affecting loneliness were professional medical team support, life satisfaction, and personality, perceived health status, complication and family support, which explained about 21.8% of the variance. Conclusion: The results of this study indicate that nursing intervention is needed to reduce loneliness, and to improve the perceived health status, social support and life satisfaction in the hospitalized patient with pneumoconiosis. These results can provide for evidence of nursing intervention to facilitate reduction of loneliness.

• 대한간호학회지
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• 제41권3호
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• pp.374-381
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• 2011

Purpose: The purpose of this study was to develop and validate a hospice palliative care performance measure which would cover more than just physical symptoms or quality of life. Methods: Through an intensive literature review, the author chose questions that measured aspects of physical, emotional, spiritual, social, or practical domains pertinent to hospice palliative care for inclusion in the scale. Content validation of the questions was established by 15 hospice palliative care professionals. A preliminary Hospice Palliative Care Performance Scale (HPCPS) of 20 questions was administered to 134 pairs of terminal cancer patients from 5 hospice palliative care units and their main family caregiver. A validation study was conducted to evaluate construct validity and internal consistency. Results: Factor analysis showed 14 significant questions in five subscales; Physical, Emotional, Spiritual, Social, and Patient' rights. There were no significant differences between the ratings by patients and family members except for three out of the 14 questions. The measure demonstrated construct validity, and Cronbach's ${\alpha}$ of the subscales ranged from .73 to .79. Conclusion: The HPCOS demonstrated acceptable validity and reliability. It can be used to assess effectiveness of hospice palliative care for terminal cancer patients in practice and research.

• Child Health Nursing Research
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• 제16권2호
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• pp.136-143
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• 2010

Purpose: The purpose of this study was to identify the relationship of children's behavior problems and child-rearing stress to rejective parenting attitude in mothers. Methods: Study participants were 595 mothers who had children aged 3 to 5 who attended one of 10 kindergartens or infant schools in M or B Cities. The instruments used for this study were a self-report questionnaire, CBCL (Child Behavior Check List), PARQ (Parenting Acceptance-Rejection Questionnaire), and PSI (Parenting Stress Index Short Form by Abidin). Regression analysis was the statistical method used for data analysis. Results: The factors associated with rejective parenting attitude were child-rearing stress, birth order, mother's education, the major caregiver in the family, and the type of family. These factors explained 33.7% of rejective parenting attitude. Conclusion: The findings indicate a need to develop and provide parenting programs to reduce child-rearing stress in mothers.

• 부모자녀건강학회지
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• 제18권1호
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• pp.28-38
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• 2015

Purpose: This study was conducted to identify the role and role burden of caregivers with hospitalized children. Methods: The participants included 149 main caregivers from two pediatric hospitals whose children have been hospitalized for at least 2 days at children's hospital. The data were collected from August 1 to september 30, 2013 using self-report questionnaires of checklist type for caregivers' role and Likert scale for role burden. Results: Role for hospitalized children showed that personal hygiene was the highest, and consultation with nurses and doctors was the lowest in total frequency per day. Of the role for the caregivers themselves and family, personal hygiene was the highest, and home management was the lowest. The degree of role burden perceived by hospitalized children's caregivers was the slightly high. Of the categories, emotional burden was the highest and dependent burden was the lowest. There were differences by caregivers' age, children's age, and children's health status. Conclusion: The caregivers performed various roles, especially more frequently on personal hygiene and nutrition for their hospitalized children and themselves and family, and had slightly high role burden. These results may contribute to develop nursing interventions that can help adapt on hospitalization of children and their caregivers.

• 가정과삶의질연구
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• 제20권4호
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• pp.13-26
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• 2002

The purpose of this study was to understand the adult day care as a place for the elders and adults and to develop an initial understanding of the programs and their participants for adult day care for the cognitively-impaired in the U.S.A. The data was collected from 13 Adult Day Care Centers(ADC), and 318 participants from six Adult Day Care Centers from 2001 to 2002 by personal interview and the documents about the participants and their family and caregivers. Participants used ADC program average 8.15 hours In weekdays, 3 days per week. ADC programs provided primarily lunch and snack, transportation, personal care, professional health care, occupational.speech physical therapies, rehabilitation, and respite care. Participants'caregivers were mainly daughters and wives. It is the hope of this study to provide design and care professionals with a first draft of a ″sense-making″template by which they may understand adult day care in a systemic manner and engage in meaningful results as to what this place type could and should be.

• 종양간호연구
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• 제12권3호
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• pp.221-229
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• 2012

Purpose: The purpose of this study was to identify correlates influencing cognitive impairment in breast cancer patients receiving chemotherapy. Methods: Study subjects consisted of 102 breast cancer patients who received chemotherapy. Subjects were the members of a breast cancer self-help group. Data were collected using structured self-reporting questionnaires including scales of cognitive impairment, physical status, fatigue, quality of life, emotional status, sleeping, family support, and menopausal symptoms. Statistical Package for Social Sciences was used for statistical analyses. Results: Breast cancer patients receiving chemotherapy appeared to show a high level of cognitive impairment. Among demographic characteristics, the effects of economic status and family type on cognitive impairment were found to be statistically significant. Among disease related characteristics, the effect of duration of chemotherapy on cognitive impairment was statistically significant. Menopausal symptoms were positively associated with cognitive impairment. The model including postmenopausal symptoms and caregiver type explained about 66% of variability in cognitive impairment. Conclusion: These findings highlight the importance of contextual factors in understanding cognitive impairment in breast cancer patients receiving chemotherapy and can be used to develop appropriate, effective nursing interventions.