• 한국노년학
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• 제31권4호
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• pp.871-884
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• 2011

표준장기요양이용계획서는 노인장기요양보험 이용자와 가족의 급여이용을 지원하기 위한 목적으로 도입된 일종의 케어플랜이라고 할 수 있다. 본 연구는 가족수발자가 인지하는 표준장기요양이용계획서의 질과 만족도, 활용도를 파악하고 이들 간의 관계를 파악하는 것을 목적으로 한다. 연구자료는 2008년 11월~12월 현재 노인장기요양보험 1~3등급 판정을 받고 재가장기요양서비스를 이용하고 있는 수급자의 가족수발자를 대상으로 가정방문면접조사를 통해 수집하였고, 총 944명의 가족수발자 가운데 표준장기요양이용계획서를 읽어본 경험이 있으며 설문을 완성한 351명이 최종분석대상이 되었다. 조사도구는 가족수발자와 수급자의 인구사회학적 특성 및 장기요양특성, 질 측정항목(9개), 전반적 만족도 측정항목(1개), 활용도 측정항목(2개) 등을 포함하였고, 질, 만족도 및 활용도 간의 관계를 파악하기 위해 경로분석을 실시하였다. 연구결과, 표준장기요양이용계획서의 질은 장기요양 욕구평가 영역, 장기요양 이용계획 영역, 월 한도액 관리지원 영역 등 세 개 영역으로 구분되었고, 모든 영역이 만족도 및 활용도와 유의한 상관관계를 나타냈다. 다음으로 경로분석 결과, 표준장기요양이용계획서의 장기요양 욕구평가 영역의 질(간접효과, 경로계수=0.077)과 전반적 만족도(전체효과, 경로계수=0.324)가 활용도에 통계적으로 유의한 영향을 미쳤다. 본 연구결과는 표준장기요양이용계획서의 역할을 향상시키기 위한 전략을 개발하는데 도움이 될 것으로 기대된다.

• 한국사회복지학
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• 제18권
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• pp.175-205
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• 1991

• 대한간호학회지
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• 제37권5호
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• pp.693-702
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• 2007

Purpose: The purpose of this study was to develop and evaluate the effects of a support group intervention on the burden of primary family caregivers of stroke patients. Method: A nonequivalent control group pretest-posttest design was used. The subjects were 36 primary family caregivers of stroke patients [experimental(N=18) and control(N=18) groups] in a neurosurgery ward of a university hospital. The experimental group members participated in six sessions of a support group intervention for two weeks and the degree of their caregiving burden was evaluated. Data was analyzed by Chi-square tests, t-tests, and paired t-tests using SPSS 10.0. Result: The experimental group had a significantly lower total burden score (t=2.06l, p= .047)and sub-scales of emotional(t=-3.319, p= .002), time-dependent(t=-2.045, p= .049) and developmental(t=-2.656, p= .012) burden scores than the control group, while no significant differences were found in physical, social or financial burden scores between the two groups. Within the experimental group, there was a significant decrease in physical(t=2.507, p= .023), emotional(t=4.754, p= .000), social(t=2.932, p= .009), time- dependent(t=5.015, p= .000) and developmental(t=7.541, p= .000) burden scores but not the financial burden score. Conclusion: The results suggest that a support group intervention can be utilized as an effective nursing program to reduce the burden of primary family caregivers of stroke patients.

• 여성건강간호학회지
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• 제17권3호
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• pp.285-293
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• 2011

Purpose: This study was designed to examine the relationship between perceived entrapment to depression and subjective well-being of women as family caregivers caring for elderly dementia patients. Methods: One hundred and sixty-nine women family caregivers were recruited from two high schools located in Seoul, Korea for this descriptive study. The instruments used were The Entrapment Scale, The Center for Epidemiology Studies Depression Scale (CES-D) and Subjective well-being scale. Results: The score of perceived entrapment significantly correlated with depression and subjective well-being. The significant predictor of depression in women caregivers was perceived entrapment, 50.3% of the variance in depression. Also, perceived entrapment was predictor of subjective well-being in women caregivers, explaining 41.4% of the variance in depression. Conclusion: This study showed that perceived entrapment is an important predictor for depression and subjective well-being. Therefore, in order to reduce depression in women caregivers, it is necessary to design an intervention program that helps with coping and reduces perceived entrapment.

• 지역사회간호학회지
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• 제23권4호
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• pp.347-357
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• 2012

Purpose: The purpose of this study was to explore the experiences of family caregivers who care for the elderly under Long-term Care Insurance. Methods: Data were collected using focus group interviews and analyzed using a phenomenological approach. The four focus groups consisted of eight caregivers, two social workers and three nurses in B city, Korea. Results: Five themes were identified: 'Obtaining a care-helper certification for employment', 'Taking care of the elderly in their homes', 'Difficulties due to life changes', 'Difficulties due to reduced wages' and 'Dissatisfaction with the Long-term Care Insurance operating system'. Conclusion: The results of this study demonstrate that the long-term care system for family caregivers faces many systematic challenges in providing care for the elderly harmoniously in their home. To help them succeed in their tasks, Long-term Care Insurance system must offer respite and support programs to family caregivers.

• 지역사회간호학회지
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• 제22권4호
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• pp.389-398
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• 2011

Purpose: This study of this study was to identify factors influencing the burden of main family caregivers who take care of elderly patients with brain and spinal diseases. Methods: This was conducted as descriptive research and data were collected from 255 main family caregivers who were taking care of elderly patients with brain and spinal diseases from 4 hospitals in Daegu and Gyeongbuk Province. Stepwise-multiple regression was used to identify the influencing factors of burden felt. Results: As the score of burden felt by the main family, economic, social, physical, interdependent and emotional burdens were high in order. Factors influencing burden felt by main family care givers taking care of elderly patients with brain and spinal diseases were changed relation with patient after hospitalization, daily life ability, marital status, education and family caregiver's personality (explanatory power of 24.6%). Family caregivers felt a heavier burden when their relation with the patient was changed negatively or when the patient's activity of daily living was low. Conclusion: Based on these results, we need to develop coping measures and interventional programs for reducing the burden felt by the main family caregivers of elderly patients with brain and spinal diseases.

• 대한가정학회지
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• 제49권10호
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• pp.15-27
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• 2011

The predominant concern of the study consists in:(1)the positive direct effects of both individual's intimacy toward parents and individual's self-efficacy of care-giving roles on individual's care-giving commitment; (2)the positive mediating effect of individual's self-efficacy of care-giving on individual's care-giving commitment; (3)the moderating effect of the degree of unhealthy condition of individual's elderly parents on each causal relationship. For conducting this study, a survey method was used on 318 males with parents at the aged of 45-60, residing in Daegu and KyungPook. In order for subjects to verify research questions, structural equation models were explored. The findings of the study supported the direct, indirect effect and moderating effects, which suggested in research questions. Participants with unhealthy parents showed greater tendency in terms of influencing their intimacy toward parents on care giving commitment than participants with healthy parents did. The above findings claimed our attention in that provided a range of practical implication.

• 폴리머
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• 제27권5호
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• pp.436-442
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• 2003

에틸렌-프로필렌 디엔 고무 (EPDM)와 같은 열경화성 탄성체는 자동차의 스폰지 웨더스트립 (sponge weatherstrip)에 적용되는 주 재료이다. 그러나 열경화성 탄성체의 특성 때문에 환경적인 문제가 야기된다. 더구나 EPDM 재료의 weatherstrip 제조 시 배합, 가류와 같은 여러 생산 공정을 거쳐야 함으로 생산 단계별 품질산포가 크고 제품의 형상 유지가 어려워 품질의 안정성이 떨어진다. 따라서 재활용과 획기적인 제조기술 그리고 수발포를 할 수 있는 새로운 열가소성 가황체 (TPV)재료 개발로 종래의 EPDM 웨드스트립 제조 문제들을 개선이 필요하게 되었다. 본 연구에서는 TPV 수발포 공정에서의 발포체의 밀도와 구조적인 면을 물의 양과 발포 온도 등의 가공 조건들의 영향을 수행하여 TPV가 수발포로서 균일한 발포체를 얻을 수 있다는 것을 알 수 있었다. 연구결과 EPDM 웨더스트립의 많은 재활용이 곤란한 문제점 등을 해결할 수 있고, 이 새로운 발포 기술은 고무산업에 돌파구를 만들어 나갈 것으로 기대된다.

• 한국사회복지학
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• 제59권2호
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• pp.65-88
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• 2007

본 연구의 목표는 서양에서 가족수발자가 돌보는 노인의 인지적 기능을 평가하기 위해 개발된 기억 및 행동문제 개정점검표를 우리나라 요보호노인의 가족수발자에게 맞게 수정하여 한국형 기억 및 행동 문제 개정점검표를 제시하는 것이다. 연구에 참여한 가족수발자 387명을 무작위로 두 집단으로 나눠서, 연구 1에서는 기억 및 행동문제 개정점검표의 신뢰도, 탐색적 요인, 수렴 및 기준 타당도 분석을 실시하였고, 연구 2는 연구 1에서 제시한 한국형 기억 및 행동문제 개정점검표의 신뢰도 분석, 확증적 요인분석, 수렴 및 기준 타당도를 검증하였다. 본 연구결과는 수정된 척도(K-RMBPC)가 노인의 기억 및 행동문제를 측정하기 위한 도구로서 적절함을 통계적으로 보여주고 있다. 이는 사회복지 연구와 실천현장에서 노인의 인지적 기능을 더욱 정확하게 측정할 수 있는 틀로 사용될 것으로 기대한다.

• 기본간호학회지
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• 제18권3호
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• pp.337-347
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• 2011

Purpose: Purposes of this study were to develop a community-based respite program for family caregivers and to test the effects of the program. Methods: Focus group interviews were performed to extract meaning of respite care for family caregivers (13 participants) and a survey was done to identify respite needs of family caregivers (157 participants). The community-based respite program for family caregivers was developed based on results of the focus group interview and survey. The program was used with 41 participants (19 experimental and 22 control). Independent t-test and Mann-Whitney U-test were used to test differences between control and experimental groups for respite needs, burden of caregivers, subjective wellbeing, social support, fatigue and functional status of elders with dementia. Results: There were statistical differences in caregiver burden, subjective wellbeing, and social support after the program, but, none for respite needs, fatigue and functional status of elders with dementia. Conclusion: The results indicate that a respite program can be useful to decrease burden of caregivers and increase subjective wellbeing and perceived social support of family caregivers in community settings. Further intervention research is needed to increase the functional status of elders with dementia and decrease fatigue in caregivers.