• 한국생활과학회지
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• 제7권2호
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• pp.1-10
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• 1998

The purpose of this study are to examine the influential variables between general character, family system, coping strategies, social support and stress of main caregivers for disordered elderly family. This study was conducted by interviewing of 177 family-members care to giving disordered elderly families in Taegu and Kyeongbuk province. The data were analyzed with the SPSS statistical package using frequency and percentage, multiple regression and path analysis. The results of this study were as follow : The variables influencing stress related to the disordered elderly family are the degree of disorder (${\beta}=.348^{***}$), caring-time-per day (${\beta}=.303^{***}$), employment status of main caregivers (${\beta}=.223^{***}$), social support (${\beta}=.241^{**}$), relational coping strategies (${\beta}=.199^{**}$), problem-avoidance coping strategies (${\beta}=.327^{***}$). Thus, in disordered elderly families, a high-stress situation arises with a highly-educated caregiver when problem-avoidence coping strategies or relational coping strategies are used or when daily caring time is great. A low-stress situation results when the caregiver is employed and the social support level is high.

• 한국지역사회생활과학회지
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• 제18권1호
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• pp.71-85
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• 2007

This study investigates differences by type of caregiving using data on three groups of caregivers, 177 from home stay situations, 189 from day care centers, and 138 from nursing homes. First, the result shows that characteristics of both caregivers and elders differ by type of caregiving. Second, caregivers in the home stay situation have the highest caregiving burden of the three groups. Third, from examination of the related variables, the caregiving burden of home stay caregivers is affected by family income, caregivers' health, type of job, and whether or not the elder has symptoms of dementia. Also, the study reveals that emotional services for elders reduce the aggravation of family relations and economic burden, but that instrumental services highly increase economic burden. It reveals that caregivers of elders in day care centers, especially those who are in bad health, are more likely to experience feelings of constriction, aggravation of family relations and economic burden. On the other hand, caregivers who receive more emotional services have better experiences in family relations, including relations with the elder. In case of the elders of nursing homes, if the main caregiver is a daughter-in-law, aggravation of family relations is higher than if the main caregiver is a spouse. Finally, the caregiver's burden is affected by their own health and income, and by whether the elder has symptoms of dementia or stroke.

• 사회복지연구
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• 제44권3호
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• pp.31-56
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• 2013

한국에서 2008년부터 시행된 노인장기요양보험제도는 요양욕구가 인정된 모든 노인에게 장기요양서비스 공급이라는 사회적 지원을 제도화하였다. 이를 계기로 한국 노인돌봄의 사회적, 제도적 환경은 새롭게 형성되었다. 이러한 새로운 조건에서 가족돌봄의 위치와 의미를 재조명하고자 하는 것이 본 연구의 문제의식이다. 이를 위해 공식적인 돌봄서비스를 이용하는 노인들에 대한 가족돌봄의 변화를 분석하였다. 분석의 초점은 공식과 비공식, 제도적 서비스와 가족돌봄의 통합으로서 노인돌봄의 양상을 파악하고 이 안에서 공식적 돌봄의 역할과 가족돌봄에서 일어난 변화를 파악하는 데 있다. 이를 위해 노인장기요양보험제도를 이용하는 가족돌봄자(노인의 배우자 및 자녀) 중 재가서비스 이용자 18명을 대상으로 심층면접조사를 실시하였고, 질적내용분석을 통해 연구결과를 도출하였다. 연구 결과, 표준화된 방문요양 및 방문목욕 등 노인장기요양서비스는 개별 사례별로 상이한 비중과 의미로 이용되고 있었다. 공식돌봄과 비공식 가족돌봄의 결합양상은 다양하게 나타났는데 본 연구에서는 네 가지 서로 다른 양상을 발견할 수 있었다. 요양보호사에 의한 노인장기요양서비스를 중심으로 노인돌봄을 구성하는 양상, 가족돌봄자가 다양한 돌봄자원을 동원하며 조정하는 역할을 하는 돌봄혼합의 양상, 중증노인이 재가서비스를 이용하면서 형성되는 노인돌봄의 양상, 그리고 무엇보다 노인장기요양보험제도의 현실화과정에서 공식돌봄과 비공식돌봄을 일치시키는 변종(hybrid)방식으로 가족요양보호사 방식의 노인돌봄 양상이 그것이다. 본 연구는 표준화되고 공식화된 노인장기요양보험제도의 재가서비스 이용이 실제 다양한 노인의 욕구와 가족돌봄자원이라는 현실을 만나면서 다양한 노인돌봄의 양상으로 현실화되고 있는 것을 드러냈다는 데 의미를 가진다. 이는 노인돌봄이 공식, 비공식 돌봄의 결합으로 작동하고 있음을 증명하는 것이며 공식적 돌봄서비스의 공급이 실제 가족돌봄의 조건과 현실 위에서 이루어져야 한다는 것을 보여준다. 따라서 노인장기요양서비스 공급에서 노인이용자의 삶의 조건이자 공간으로서 가족과 지역사회의 다양한 특성이 포함되어야 한다는 시사점을 준다고 하겠다.

• 기본간호학회지
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• 제15권3호
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• pp.274-283
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• 2008

Purpose. The purpose of the study was to identify the factors, which predict care burden perceived by caregivers of elders with dementia. Methods: The participants in this descriptive survey were 92 caregivers who used one of six daycare centers located in Incheon. The data were collected by questionnaires composed of items on general characteristics of the elders and caregivers, care burden, caregiver fatigue, and functional status of the elders. Results: General characteristics of the elders associated with care burden were age, gender, religion, and the presence of a spouse. Features of caregivers related to care burden were education, relationship with elderly, amount of rest, intention to care, monthly family income, and perceived family economic status. There were significant correlations among care burden, fatigue of caregiver and functional status of the elders. In stepwised multiple regression analysis, significant influencing factors were identified as caregiver fatigue, functional status of the elders, intention to care, relationship with the elders, amount of rest and elder's gender. Those variables explained 46% of variance of care burden. Conclusion: Functional status of elders and amount of rest were significant predictors and are supported by other previous studies. Future interventions for caregivers need to be focused on the slowing down of functional status of elders and increasing of number and length of caregiver's rest periods.

• 디지털융복합연구
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• 제12권12호
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• pp.61-76
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• 2014

본 연구는 노인요양병원에 입원한 환자보호자를 대상으로 소비가치와 병원 만족도 및 환자보호자의 심리적 안녕감 간의 관계를 조사하는데 목적이 있다. 본 연구를 위하여 서울 경기지역에 소재한 민간노인요양병원 10개소에 입원하고 있는 환자보호자를 대상으로 설문조사를 실시하여, 총 355부의 자료로 분석을 수행하였다. 분석방법은 SPSS 18.0을 이용하여 요인분석을 통한 타당도 분석, 신뢰성 검토와 다중회귀분석법을 시행하였다. 연구결과 노인요양병원의 소비가치 중에서 기능적 가치, 감정적 가치가 병원 만족도에 정(+)의 영향을 미쳤고, 진귀적 가치는 병원 만족도에 부(-)의 영향을 미치는 것으로 나타났다. 병원 만족도는 환자보호자의 심리적 안녕감에 정(+)의 영향을 미쳤다. 또한 가족지지가 기능적 가치와 병원 만족도 간의 관계에서 조절변수로서 역할을 하였고, 환자보호자의 심리적 안녕감에 직접적인 영향을 미치는 것으로 나타났다. 이 연구결과의 함의를 논의하고, 환자보호자의 병원 만족도와 심리적 안녕감을 향상시킬 수 있는 병원경영 연구과제를 제시하였다.

• 한국노년학
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• 제30권4호
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• pp.1117-1127
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• 2010

본 연구는 치매노인 가족의 부담감, 대처능력과 삶의 질을 파악하고 그 관계를 확인하기위해 구조화된 설문지를 이용해 시행된 서술적 조사연구이다. 연구의 대상자는 치매주간보호센터에 등록되어 서비스를 받고 있는 65세 이상 치매 진단자의 가족으로 경기도 일개 시 주간보호센터 8곳을 임의 표출하여 2010년 4월부터 6월까지 조사하였고 최종 연구대상자는 탈락자를 제외한 93명이었다. 연구결과 치매노인 가족의 부담감과 대처능력, 건강관련 삶의 질 정도를 확인하였고 부담감은 연령, 학력, 직업에 따라 차이가 있었으며 대처능력은 학력과 월소득에 따라, 건강관련 삶의 질은 연령과 결혼형태, 치매노인과의 관계에 따른 차이가 있음을 확인하였다. 본 연구의 의의는 건강관련 삶의 질과 대처능력, 부담감간의 관계를 확인함으로써 건강관련 삶의 질 향상을 위한 중재개발에 기초자료를 제시한 것이며 앞으로 대처능력 향상을 위한 구체적 연구와 치매노인 가족의 대처능력이 스트레스와 부담감에 미치는 영향에 대한 연구가 확대될 것을 제언한다.

• 한국노년학
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• 제29권2호
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• pp.407-424
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• 2009

본 연구의 목적은 일상생활을 독립적으로 수행하기 어려워 도움이 필요한 노인을 돌보는 가족부양자의 부양경험을 다차원적으로 평가하기 위해 서양에서 개발된 부양자반응척도(CRA)를 우리나라 가족부양자에게 적합하도록 수정하여 한국형 부양자반응척도(K-CRA)를 제시하는 것이다. 이를 위해 우리나라 가족부양자를 대상으로 부양자반응척도(CRA)를 조사한 결과를 문항분석, 탐색적 요인분석, 타당도분석 등을 실시하였다. 연구의 대상은 조사시점을 기준으로 6개월 이상동안 일주일에 최소 7시간 이상의 돌봄을 일상생활수행능력에 제약이 있는 노인에게 제공한 253명의 가족부양자이었다. 분석결과를 통해 최종적으로 수정된 한국형 부양자반응척도(K-CRA)가 만족스러운 수준의 내적신뢰도, 구조적 타당도, 기준타당도, 수렴타당도를 지닌 것으로 나타났다. 본 연구를 통해 제시된 한국형 부양자반응척도(K-CRA)는 노인복지연구와 실천현장에서 가족부양자의 경험을 다차원적으로 평가할 수 있는 도구로 활용될 것으로 기대된다.

• Child Health Nursing Research
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• 제6권2호
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• pp.199-211
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• 2000

Today, more chronically ill and handicapped children are being cared for at home by a family member caregiver. The task of caring for a family member may feel burden that the caregiver has less time and money and more work. Family functioning and their burden have influence on coping and adaptation of families with chronically-ill children. This study attempted to identify the levels of burden and family functioning in families of children with cerebral palsy and to examine their relationships. The instruments were burden scale developed by Suh and Oh(1993), and a modified Feetham Family Functioning Survey based on Roberts and Feetham.(1982). The subjects were 98 parents of children, under 15 years, who have cerebral palsy and being treated and living in Pusan. Data were collected through a self-administered question- aire from April 26 to May 29. The collected data were tested using frequencies, percentiles, means, t-test, ANOVA, and Pearson correlation coefficient with SPSSWIN program. The results of this study were as follows ; 1. The mean rating scores of burden and family functioning were 2.79±.51 and 4.12±.69, respectively. 2. The relationships between general character- istics and burden were statistically significant difference : degree of children's handicap(F=6.333, P<.01). The relationships between general characteristics and family functioning were statistically significant differences : familial relation with the children(F=3.628, P<.05), caregiver's health status(F=4.359, P<.05), age of children (F=4.185, P<.05), and duration of treatment (F=6.802, P<.01). 3. In families of children with cerebral palsy, there was significantly negative correlation between the burden of parents and the performance of family functioning(r=-.230, P<.05). There were significantly negative correlations between the burden of parents and the satisfaction of family functioning (r=-.211, P<.05), and between the perceived importance and the satisfaction of family functioning(r=-.481, P<.01); however, there was a positive correlation between the performance and the perceived importance of family functioning(r=.425, P<.01). In conclusion, this study suggests that families of children with cerebral palsy need family-focused nursing interventions as supportive care for relieving their burden and for improving family functioning.

• 기본간호학회지
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• 제4권2호
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• pp.175-192
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• 1997

The purpose of this study was to identify the care needs of family-caregivers to the patients with stroke. Subjects were 115 family-caregivers caring for the patients while they were in-patients or out-patients with stroke in two general hospitals and one oriental medicine hospital located in Seoul and Kwang-Ju. The instrument used for this study was made by the researcher on the basis of results of literature review and interviews with family-caregivers, composed of 35 items. Internal validity by calculation of cronbach's alpha with data of respondents was 0.91, which was regarded as high. The Data were analyzed by SAS program, with percentage, mean, t-test, and ANOVA. Factor structures of care needs of family-caregivers were elicited by factor analysis(PCA, Varimax rotation). Datum collection had been from July 1 to August 14, 1997. The results of this study were as follows : 1. The mean score of the sum of the care needs of family-caregivers was 3.96 and the highest-mean item was 'need for immediate care(M=4.77)', and the lowest-mean item was 'need for chaplian's visit (M=2.82)'. 2. Care needs of the family-caregivers were : Need to be informed of the disease, treatment and care ; need of education and assistance related to physical functional level ; need of social support and consultation ; need of management of nursing problem related to immobility ; need of appreciation ; need of the way to communicate with patients ; need of immediate care and help. The highest mean factor was the 'need for immediate care and help(M=4.74)', and the lowest mean factor was the 'need of appreciation(M=3.58)'. 3. The variables influencing the degree of care needs perceived by family-caregivers to the patients with stroke were as follows : There were significant differences between need to be informed of the disease, treatment and care and general characteristic factors, which were family caregiver's sex (p=.0178), caring period(p=.0223) and patient's suffering period(p=.0244). There were significant differences between need of education and assistance related to physical functional level and general characteristic factors, which were patient's paralysis(p=.0177), patient's ADL dependency(p=.0032). There were significant differences between need of social support and consultation and general characteristic factors, which were family caregiver's sex(p=.0055), occupation(p=.0159), religion(p=.0093) and patient's sex(p=.0134). There was significant difference in the degree of need of management of nursing problem related to immobility, according to the patient's ADL dependency(p=.0493). There were significant differences between need of appreciation and general characteristic factors, which were family caregiver's age(p=.0107), sex(p=.0133), and patient's age(p=.0338). There were significant differences between need of the way to communicate with patient and general characteristic factors, which were patient's paralysis(p=.0002) and aphasia(p=.0001). There were significant differences between need of immediate care and help and general characteristic factors, which were family caregiver's caring period(p=.0162) and patient's suffering period(p=.0116). 4. The mean score of patient's ADL dependency was 3. 38 and the highest-mean item was 'ascending and descending stairs(M=4.12)', and the lowest-mean item was 'drinking(M=2.60)'. There was no significant difference in the degrees of care needs related to the patient's ADL dependency. 5. The highest information source of family-caregivers was from the doctors about the disease, treatment and care(26.1%). The second highest one was from mass media(20.8%), and the third one was from the nurses. The above findings may be used as the basic data to seek more efficient way of elevating nursing practice and quality for family-caregivers to the patients with stroke.

• 한국보건간호학회지
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• 제14권1호
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• pp.41-60
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• 2000

This study was designed and undertaken to identify the related factors of family caregivers' depression & quality of life with stroke elderly patient. The data was collected from August 16th to September 5th. 1999. The subjects in this study were 70 caregivers and 70 patients with stroke who were hospitalized in 2 oriental medicine hospitals and 3 hospitals located in Junla-buk do. The data was analized using percentage. means. t-test. ANOVA and pearson's correlation coefficients, step-wise multiple regression done with the SAS program. The results of this study are as follows; 1. The score for family caregivers' depression was 45.2 when total score was 80. The family caregivers who got more than 50 scores belongs to highly depression group amount to $29\%$. 2. The score for family caregivers' quality of life was 37.04 when total score was 56. 3. In the significant relationship between family caregivers' depression and general characteristics of the family caregivers ; age. sex, income. In the significant relationship between family caregivers' quality of life and general characteristics of family caregivers: age, education, income. In the significant relationship between family caregivers' depression and quality of life and general characteristics of stroke elderly patient ; sex. 4. The depression degree showed significant differences in the variables of family caregiver's physical health(r=-0.307, p=0.011), stress(r=0.463. p=0.011). social support (r=-0.241. p=0.046) and elderly stroke patient's ADL(r=-0.313, p=0.009). The quality of life degree showed significant differences in the variables of family caregivers' depression(r=-0.564, p=0.001), stress(r=-0.322, p=0.008), social support (r=0.353. p=0.003). 5. The most important variable affecting family caregiver's depression was caregivers' physical symptom which accounted for $32.0\%$ of the total variance in which multiple regression analysis. Total variance affecting the family caregivers' depression was $49\%$. The most important variable affecting family caregivers' quality of life was caregivers' depression which accounted for $48\%$ of the total variance in which multiple regression analysis. Total variance affecting the family caregivers' quality of life was $61\%$.