• 가정과삶의질연구
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• 제23권6호
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• pp.117-131
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• 2005

In this paper, 1 examined role gratification and role strain of South Korean working mothers. The results show that South Korean working mothers experienced very similar level of role gratification and role strain as taking their multiple roles. The findings also show that the factors of caregiving demands, employment demands, caregiving resources, employment resources are not strongly related to role gratification and role strain. Among the 12 caregiving demand variables and employment demand variables, number of children, type of family, number of hours worked were significantly related to producing role gratification. Among the 12 caregiving demand variables, number of hours worked, number of husbands absence due to night work were significantly related to producing role strain. Among the 8 caregiving resources, participants satisfaction due to income contribution, look to make a purchase new electric home appliances were significantly related to produce role satisfaction. Among the 8 caregiving resources, number of family support policies in the husbands workplace, participants satisfaction due to income contribution were significantly related to producing role strain.

• 한국사회복지학
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• 제54권
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• pp.203-220
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• 2003

본 연구의 목적은 비공식 부양자가 기능제안이 있는 중증 장애노인에게 제공하는 노인보호의 양과 유형에 영향을 미치는 요인을 파악하는 데 있다. 이를 위해 65세 이상 중증장애노인을 수발하고 있는 주부양자들을 대상으로 설문조사를 하여 회수된 설문지 중에서 사용 가능한 211부를 본 연구의 분석 표본으로 선정하였다. 연구목적에 따라서 부양상태에 대한 확률 추정과 보호제공시간량에 미치는 요인을 분석한 결과, 부양상태와 부양결정에 관련된 요인들에 대하여 유의미안 결과를 얻을 수 있었다. 보호제공시간 시간량에 OLS분석을 실시한 결과에 따르면, 첫째 소득은 총가족보호시간에 회귀한 모형 1에서만 효과가 있는 것으로 나타났다. 둘째, 부양생산기술의 구성요소들 중 일상생활동작제한과 수단적 일상생활동작제안, 부양팀원수, 공식서비스 이용이 보호제공량에 유의미한 영양을 주는 것으로 나타났다. 셋째, 가계생산기술을 구성하는 요소들은 부양시수에 유의한 영양을 미치지 않는 것으로 나타났다. 넷째, 부양자 선호의 구성요소에서는 부양자의 경제활동 여부, 노인보호 구입을 위해 지불할 용의가 있는 금액이 유의한 것으로 나타났다.

• 가정간호학회지
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• 제2권
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• pp.19-34
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• 1995

The purpose of this study was to analysis level on family caregiver's burden for the elderly with chronic disease in a rural area and to choose priority care group, thereby facilitating the development of interventions to reduce the caregiver's burden. For this purpose, data were collected by questionaire from June 10 to October 8, 1994. The instruments for data collection were Caregiver Burden Inventory by Novak(1989) and Zarit et al(1982), severity of dementia by Hughes Scales(1982), ADL by Lawton(1971), patients' family caregiving activity by pre-survey and reference review(Lee, 1993 ; Jang, 1990 ; Yoo, 1982). The subjects were 213 family caregiver of elderly with chronic disease in a rural area. The data was analysed by the use of t-test, ANOVA, correlation and multiple regression. The results were as follows ; 1. Total burden was evaluated below average, the mean of family burden was 46.98. By the diagnostic classification, Hypertension was 27.37, DM 32.46, CVA 62.96, Dementia 61.24. 2. Significant variables which were correlated to the family caregiver's burden were the patient's disease diagnosis (F=33.82, p<0.001), severity of dementia(F=30.52, p<0.001), the status of disease management(F=11.53, p<0.001), ADL(F=10.54, p<0.001), PADL(F=7.50, p<0.001), income(F=7.17, p<0.001), caregiver's health status(F=24.53, p<0.001), a view of patient's prognosis (F=22.17, p<0.001), relationship with the patient(F=33.82, p<0.001), the number of hours per day spent on caregiving(F=77.52, p<0.001), level of intimacy of caregiver and patients(F=8.75, p<0.001), level of helping(F=4.90, p<0.01), the frequency of caregiving activity(F=3.80, p<0.01), the number of admission(F=5.54, p<0.01), the length of caregiving(F=4.43, p<0.01), other chronic patient in family(t=2.81, p<0.01), caregiver's job(F=3.11, p<0.01), the duration of illness(F=2.98, p<0.05), caregiver's religion(F=2.93, p<0.05), medical security(F=3.89, p<0.05), caregiving's helper(t=2.42, p<0.05). 3. PADL was the most important predictor to family caregiver burden(R2=0.6611). In addition to this, IADL, caregiver's health status, the length of caregiving. level of intimacy of caregiver and patients, patient's age, the patient's disease diagnosis and patient's job accounted for 76% of family caregiver burden. 4. The criteria of priority care group were as follows ; the mean of family caregiver burden was above 58, above of moderate ADL, the number of hours per day spent on caregiving above of 8 hours, above of moderate dementia. By the diagnostic classification, number of priority care group, Hypertension was 4 (8.0%), DM 4(8.0%), CVA 34(64.1%), Dementia 45(75.0%).

• 한국노년학
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• 제36권3호
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• pp.693-709
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• 2016

손자녀를 돌보는 한국 조모들의 돌봄 특성에 따른 우울 증상을 살펴보기 위하여 시행한 연구이다. 한국고령화연구패널조사 4차 자료(2012년) 참여자 중, 손자녀가 1명 이상인 여성은 총 3,291명이다. 이 중 손자녀를 돌본경험이 있는 127명을 대상으로 하였다. 돌봄 제공 손자녀 수, 연간 돌봄 기간 및 주당 돌봄 시간에 따라 우울증상에 차이가 있는지 다중 로지스틱 회귀분석을 실시하였다. 사회경제적 특성과 건강상태(주관적 건강, 만성질환 이환 개수, 통증 유무)를 통제하였을 때, 조모들은 손자녀 돌봄 기간이 길수록 우울 증상이 낮게 나타났고, 이와 반대로 주당 돌봄 시간이 길수록 우울 증상이 높게 나타났다. 손자녀를 돌보는 조모는 고령여성이 가지는 다양한 건강 문제와 더불어 돌봄 제공자 역할을 받아들일 수밖에 없으며, 이 과정에서 주당 돌봄 시간이 길수록 우울 증상 고위험군에 속할 확률이 높아진다. 손자녀 돌봄 특성과 정신 건강의 관련성에 대한 상세한 파악과 이해를 통해 손자녀 돌봄에 대한 사회적 책임 분담 등 지원 서비스와 정책에 대한 논의가 이어져야 하겠다.

• 가정간호학회지
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• 제2권
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• pp.60-76
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• 1995

The purpose of this study was to analysis level on family caregiver's burden for the elderly with senile dementia in a rural area and to choose priority care group, thereby facilitating the development of interventions to reduce the caregiver's burden. For this purpose, data were collected by questionaire from June 10 to October 8, 1994. The instruments for data collection were Caregiver Burden Inventory by Novak(1989) and Zarit et al(1982), severity of dementia by Hughes Scales (1982), ADL by Lawton (1971), patients' family caregiving activity by pre-survey and reference review(Lee, 1993 ; Jang, 1990 ; Yoo, 1982). The subjects were 60 family caregiver of senile dementia in a rural area. The data was analysed by the use of t-test, ANOVA, correlation and multiple regression. The results were as follows : 1. Total burden was evaluated over average, the mean of family burden was 61.24. 2. Significant variables which were correlated to the family caregiver's burden were the severity of dementia(F=30.52, p<0.001), ADL(F=5.43, p<0.01), PADL(F=6.14, p<0.01), caregiver's health status(F=6.05, p<0.01), a view of patient's prognosis(F=4.08, p<0.05), the number of hours per day spent on caregiving(F=19.64, p<0.001), level of intimacy of caregiver and patients(F=7.16, p<0.001), the frequency of caregiving activity(F=5.31, p<0.01). 3. ADL was the most important predictor to family caregiver burden(R2=0.6611). In addition to this, the severity of dementia, level of intimacy of caregiver and patient, relationship with the patient accounted for 79% of family caregiver burden. 4. The criteria of priority care group were as follows ; the mean of family caregiver burden was above 58, above of moderate ADL, the number of hours per day spent on caregiving above of 8 hours, above of moderate dementia. By the the severity of dementia, number of priority care group, mild dementia was 10(43.4%), moderate dementia 23 (92.0%), sever dementia 12(100.0%).

• 한국사회복지학
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• 제46권
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• pp.319-348
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• 2001

The primary purpose of this study is to examine the buffering effect of social welfare services on the relationship between the level of older persons' impairment and burden experienced by the family caregivers. It also assessed the level of caregiving burden as well as the effect of both older person's impairment and the characteristics of the caregivers on burden. The survey data collected from 150 community residing family caregivers was used for analyses. Findings are as follows. First, the caregivers are more burdened in the deterioration of mental health, scarce time for oneself, and the suffering of social life than in other areas of burden. Second, the more severe the physical and the mental impairment of the elder, the more burden the caregivers experience. The caregivers' characteristics such as the worse mental health, the lower level of attachment to the elder, the longer caregiving hours are also related to the higher level of caregiving burden. Third, the caregivers' use of adult day care and respite care services buffer the relationship between the level of impairment of older persons and the caregiving burden. However, social work counselling, visiting nurse, homemaker services do not have such buffering effects. Among informal support, instrumental support buffers the relationship between the elder's physical impairment and burden, while emotional support buffers the relationship between the elder's mental impairment and burden. According to the results, implication for social welfare services and practice methods for the family caregivers was discussed.

• 대한가정학회지
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• 제45권6호
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• pp.61-75
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• 2007

This paper examines the intergenerational time transfers between married women and their co-residing elderly parents, and how they affect married women's labor force participation and work hour. The sample was drawn from the "2004 Time Use Survey" conducted by Korea National Statistical Office and the Heckman's 2-step model was estimated to examine these relationships. We find that women's caregiving time for their elderly parents reduces their likelihood of participating in the labor force. On the contrary, parental time transfers for married women increases the probability of their labor force participation. We find no evidence that the actual hours of paid work is related to the time transfers between married women and their elderly parents. In other words, after married women decide to participate in the labor force, their work hours are not affected by the time spent for parents and time gained from parents to them. Parental income is positively associated with the married women's labor force participation whereas husband's income is negatively related. The married women working in service occupation and earn salaries work longer hours than those employed as laborer and wage workers. Having older parents and owning the second home reduce working hours of married women.

• 한국간호교육학회지
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• 제25권1호
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• pp.136-147
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• 2019

Purpose: This study aimed to explore influencing factors on care burden among family caregivers for elders with dementia living at home. Methods: Participants in this study were 211 family caregivers who were taking care of elders registered at a support center for dementia located in S-gu, Seoul. Data were collected using a structured questionnaire. Data were analyzed with descriptive statistics, t-test, ANOVA, Pearson correlation coefficients, and multiple regression in SPSS WIN 23.0. Results: The care burden of family caregivers was mild to moderate ($40.31{\pm}21.50$) in this study. The factors influencing care burden among family caregivers for elders with dementia were the age, behavioral problems, and dependency in instrumental activities of daily living of demented elderly, in addition to the perceived health status and resting hours of family caregivers. Overall, these factors explained 46.5% of the total variability in care burden in this sample (F=13.01, p<.001). Conclusion: Findings from this study suggest that the characteristics of demented elderly and family caregivers can influence care burden differently. Individually tailored strategies based on the various caregiving contexts need to be developed to reduce the level of care burden among family caregivers for elders with dementia.

• 한국콘텐츠학회논문지
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• 제16권3호
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• pp.649-660
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• 2016

본 연구는 입원 중인 뇌졸중 환자 주돌봄자의 돌봄 부담감, 대처행동, 자아탄력성 및 관계를 파악하기 위한 조사연구이다. 연구대상은 C시 S대학교 부속병원 신경외과, 신경과에 입원한 뇌졸중 환자의 주돌봄자 74명이었고, 자료수집은 2014년 3월 23일부터 9월 30일까지 이루어졌다. 연구결과, 돌봄 부담감은 3.66점, 대처행동은 2.67점, 자아탄력성은 3.10점이었다. 돌봄 부담감은 성별, 연령, 환자와의 관계, 교육수준, 결혼상태, 주관적 건강상태, 대처행동은 결혼상태, 돌봄시간에서 유의한 차이를 보였고, 자아탄력성은 유의한 차이를 보인 변수가 없었다. 돌봄 부담감, 대처행동 및 자아탄력성은 상관관계가 없는 것으로 나타났다. 결론적으로 주돌봄자의 돌봄 부담감은 크며, 돌봄 부담감을 감소시키기 위한 정부 병원 차원의 보호자 없는 병동, 포괄간호서비스 실시와 간호부의 주돌봄자를 위한 상담, 교육, 지지간호가 절실히 필요하며, 세 변수간의 관계를 밝힐 수 있는 반복 연구가 필요하다.

• Journal of Hospice and Palliative Care
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• 제19권1호
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• pp.61-69
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• 2016

목적: 말기암환자 가족 간병인의 간병 부담을 줄이는 것은 가족뿐 아니라 환자를 위해서도 중요하다. 본 연구에서는 말기암환자 가족 간병인의 간병 부담과 관련된 요인에 대해 살펴보았다. 방법: 국내 7개 기관의 완화의료병동에서 입원치료를 받는 말기암환자의 가족 간병인 289명의 자료를 분석하였다. 간병인이 느끼는 주관적 간병 부담은 암환자 가족 돌봄 경험 평가도구를 사용하였고, 5가지 차원에서 단계적 변수 선정을 사용한 로지스틱 회귀 모형을 통해 유의한 인자를 확인하였다. 결과: 간병부담의 각 차원에서 다양한 인자들과의 관련성이 확인되었다. 감정적 요인은 가장 폭넓은 영향을 미쳤는데, 감정적 스트레스를 가진 군은 그렇지 않은 군에 비해, 생활패턴이 변할 가능성이 2.54배(95% confidence interval, 1.29~5.02), 가족의 협조가 부족할 가능성이 2.27배(1.04~4.97), 그리고 신체적 부담이 커질 가능성이 5.44배(2.50~11.88)였다. 가족기능은 가족의 협조부족을 매우 잘 반영하였으며, 심한 가족기능 장애를 보일 경우 경제적 부담과도 관련이 있었다. 종교를 가진 군과 동반질환이 없는 군에서 오히려 간병 부담이 더 높은 것으로 나타났으며, 간병기간과 하루 중 간병시간은 생활패턴의 변화와 신체적 부담을 유의하게 예측하였다. 직업을 가지고 있거나, 사회적 지지가 부족하거나, 자주 방문하지 못하는 가족 간병인은 낮은 자아 존중감을 보였다. 결론: 본 연구 결과에 의하면, 가족 간병인의 간병 부담을 파악하기 위해서는 그들의 정서상태와 가족기능을 파악하는 것이 도움이 되며, 사회적 지지체계를 포함하여 경제적 부담을 완화시키는 노력이 필요하겠다.