• 지역사회간호학회지
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• 제19권2호
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• pp.216-225
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• 2008

Purpose: This study was to explore the level of health status, burnout, and burden of primary family caregivers of the elderly in-patients, and to identify the relations among the factors. Method: The subjects were a total of 232 primary family caregivers of elderly in-patients at K and E Medical Center, and were surveyed from March 1 to April 10, 2007. Measures were a health status measuring tool based on CMI developed by Brodman et al. (1945), the burnout measuring tool developed by Pines et al. (1981), and the burden measuring tool revised by Jung, Soo-Jin (1998). Data were analyzed by SPSS-WIN 12.0. Results: Firstly, the mean of health status was 1.69, which means that they were mostly healthy, and the mean of burnout was 2.66, which means that they were a little burned out. The mean of burden was 2.71, which means that they were a little burdened. Second, there were high correlations between health status and burnout, between health status and burden, and between burnout and burden. Third, there were significant difference in health status and burnout according to sex and relationship, and in burden according to sex, education level and relationship. Conclusions: Nurses need to consider the characteristics, health status, burnout, and burden of primary family caregivers.

• 재활간호학회지
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• 제13권1호
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• pp.5-12
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• 2010

Purpose: The purpose of this study was to examine the psychometric properties of the Korean version of the General Practitioner Assessment of Cognition (K-GPCog) scale. Method: The K-GPCog consists of the 2 subscales, patients and caregivers. Using a sample of 412 community-based Korean older adults, internal consistency reliability was estimated using Cronbach's alpha. To evaluate validity of the K-GPCog, correlational analysis was conducted using Pearson r between K-GPCog and the Korean Dementia Screening Questionnaire (KDSQ). Results: Cronbach's alpha coefficients of the K-GPCog patients' and caregivers' subscales .788 and .794 respectively. Pearson's correlation coefficients were r=-.374, r=-.481, and r=-.493, respectively for the subscales of patients and primary caregivers, and total K-GPCog. The degree of diagnostic agreement about the risk for cognitive disorders of older adults showed 11.7% and 11.2% respectively for the K-GPCog and the KDSQ. Conclusion: The findings provided preliminary evidence of the K-GPCog as a useful screening measure for detecting mild cognitive disorders of Korean older adults. The K-GPCog is particularly useful to identify cognitive disorders from primary caregivers when it is difficult to assess the level of cognition of older adults.

• 간호행정학회지
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• 제18권4호
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• pp.402-413
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• 2012

Purpose: This study was done to explore factors related to amount of service use for elders with long-term care needs. Methods: A descriptive-correlation design was used. The sample included 259 elders and their primary caregivers who had cared for the elders for at least 6 months. Data on long-term care need assessment, service use and interviews with primary caregivers were analyzed. Results: There was no significant relationship between the sociodemographic characteristics and the amount of services use. Amount of service use differed significantly by Long-term care classification. The mean scores for class 1, 2 and 3 were 22.68, 21.47 and 17.87 days respectively. Primary caregiver relationship with the elders and the number of family-friend helpers were also significant. Multivariate regression analysis showed that gender, marital status, activities of daily living, cognitive impairment, and secondary caregiver support explained 17% of the total variance of service use among these elders (F=3.50, p<.001). Conclusion: The results of this study indicate that critical factors including secondary caregiver support and individual background, and other functional dependencies except for physical function should be considered in accurately predicting the amount of service use for community dwelling elders with long-term care needs.

• 성인간호학회지
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• 제20권3호
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• pp.443-451
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• 2008

Purpose: This study is to examine how dementia day care service affects fatigue, depression and life satisfaction of caregiver. Methods: The study was conducted using a convenient sampling method from 6 Dementia Day Care Center in Incheon. Thirty nine primary caregivers answered the questionnaires. Pre-test was done before demented elders start using the dementia day care center and post-test was done five months after. Data were analyzed by using descriptive statistics and paired t-test. Results: There was a significant difference in caregivers' fatigue level after using dementia day care service(t=2.188, p=.035). Results of subcategories were as follows; There was a significant difference in caregivers' physical fatigue level(t=2.270, p=.029) and psychological fatigue level(t=2.277, p=.029) after using dementia day care service. However, there was not significant difference in caregivers' neurological fatigue level(t=1.312, p=.197). There was a significant difference in caregivers' depression level(t=3.066, p=.004) and life satisfaction(t=-2.131, p=.040) after using dementia day care service. Conclusion: The results indicated that dementia day care service is helpful for family with demented elders. Therefore it is necessary to expand dementia day care center in terms of its size and numbers in order to support increasing number of demented elders and their families.

• Asian Pacific Journal of Cancer Prevention
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• 제17권2호
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• pp.755-758
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• 2016

Background: There is little information about the objectivity of posttraumatic growth experienced by cancer patients. So, the aim of present study was to investigate the viewpoints of family caregivers regarding posttraumatic growth in cancer patients. Materials and Methods: This descriptive study was conducted in one referral medical center in East Azerbaijan Province in northwest of Iran. 120 primary family caregivers of cancer patients participated with a convenience sampling method. The Posttraumatic Growth Inventory (PTGI) and Perception about Prognosis Scale (PPS) were applied for data collection with analysis performed using SPSS statistical software. Results: Family caregivers believed that their patients had a good prognosis (score 3.95 from 5). The total score of PTGI was 60.7 (SD=18.8) that indicates a moderate level of growth as reported by family caregivers. Conclusions: Family caregivers of cancer patients have incorrect viewpoints about the prognosis of their patients and reported moderate levels of growth. These findings showed that posttraumatic growth among cancer patients is an objective phenomenon.

• 한국노년학
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• 제38권4호
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• pp.1127-1148
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• 2018

본 연구는 치매환자가 보여주는 다양한 증상의 정도가 주부양자의 케어스트레스에 미치는 영향을 살펴보고, 이에 대한 보호요인으로써 전문가지지 및 가족지지의 영향을 검증하는 것을 목적으로 한다. 이를 위해 서울, 경기, 부산 3개 지역의 주간보호센터 및 병원, 요양시설 10곳을 대상으로 한 설문조사를 활용하였다. 연구대상으로 치매 진단기간 5년 이내인 치매환자의 배우자 및 자녀부양자 191명을 선정하였고, 다중회귀분석을 통해 연구모형 검증에 대한 분석을 진행하였다. 연구결과 치매환자의 증상정도는 주부양자가 느끼는 정신적 고통인 케어스트레스에 정적인 영향을 나타냈다. 전문가지지와 가족지지의 보호효과를 검증한 결과, 전문가지지는 치매환자의 증상으로 인한 주부양자의 케어스트레스를 완화시켜주는 것으로 나타난 반면, 가족지지의 보호효과는 유의미한 영향을 나타내지 않았다. 본 연구결과는 의료진 및 사회복지사와 같은 전문가지지는 주부양자의 케어스트레스 완화에 효과적이지만 친척과 같은 가족들의 지지는 케어스트레스 완화에 효과적이지 않았음을 보여준다. 분석결과를 바탕으로 본 연구는 치매환자의 부양가족을 대상으로 한 정기적인 치매 증상에 관한 교육의 필요성, 주부양자의 케어스트레스 감소를 위한 지원 정책의 확대, 치매전문인력 구성의 확대 및 협업 시스템의 구축, 치매환자 부양가족구성원 간의 기능 증진을 위한 개입 필요성을 제언하였다.

• 한국노년학
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• 제29권2호
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• pp.701-716
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• 2009

본 연구의 목적은 치매노인을 돌보는 주가족 간호자의 부담감과 간호만족감 정도를 파악하고, 부담감과 간호만족감에 영향을 미치는 문화적, 비문화적 요인을 규명하는 것이다. 본 연구의 대상자는 서울 및 경기도 소재 13개 치매주간보호센터를 이용하는 치매노인을 가정에서 돌보고 있는 주가족 간호자 112명 이었으며, 설문지 조사를 통하여 자료를 수집하였다. 주가족 간호자의 81%가 여성이었고, 관계별로는 며느리(46%)가 가장 많았다. 주가족 간호자가 느끼는 부담감 평균점수는 49.4 이었으며, 간호만족감 평균점수는 42.3 이었다. 주가족 간호자의 부담감에 통계적으로 유의한 영향을 미치는 요인으로는 비문화적 요인들인 간호자의 건강상태(β= .421, p= .049)와 치매노인의 기억 및 행동문제(β= .183, p= .041)로 나타났다. 간호만족감에 통계적으로 유의한 영향을 미치는 요인은 문화적 요인인 가족주의(β= .466, p= .005)로 나타났다. 치매노인 가족 간호자들의 부담감을 감소시키고 간호만족감을 증진시키기 위한 서비스 프로그램들의 개발과 활용 방안이 마련될 필요가 있다.

• 대한간호학회지
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• 제36권7호
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• pp.1175-1182
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• 2006

Purpose: This study was conducted to evaluate the effects of stroke patient care education on the knowledge and practice of caregivers of stroke patients. Method: Data was collected from December 15, 2004 to March 30, 2005. The research design was a non-equivalent control group non-synchronized design. The subjects were forty primary caregivers of stroke patients who were hospitalized in a neurology unit of a university hospital. Forty caregivers, twenty in the experimental group and twenty in the control group were assigned. The experimental group participated 2 times in an education class given by the researcher Data analysis included -test, and t-test using the SPSS program. Result: Knowledge(t=5..87, p=0.00) and practice(t=5.53, p=0.00) of the experimental group were significantly different from the control group. Conclusion: The stroke patient care education developed in this study shows a significant promotion of knowledge and practice of caregivers. Thus this program can be recommanded as an intervention model for stroke patients and caregivers.

• 디지털융복합연구
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• 제19권10호
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• pp.419-425
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• 2021

본 연구는 장애아동 주 양육자의 행복감에 관련성이 있다고 규명된 요인들 간의 직접·간접효과를 분석하여, 장애아동 주 양육자의 행복감을 향상시키는 정책적인 대안을 탐색하는데 있다. 연구수행을 위해 전라북도 3개 지역을 대상으로 장애자녀의 주양육자 430명을 대상으로 수집된 자료를 활용하여 장애자녀 주 양육자의 사회적지지, 양육스트레스, 가족건강성과 행복감의 영향력에 대해서 살펴보았다. 주요 분석결과는 다음과 같다. 첫째, 사회적지지는 장애자녀주 양육자의 행복감에 직접적인 영향을 미침과 동시에 가족건강성을 통한 간접적인 영향력을 가지고 있는 것으로 나타났다. 둘째, 장애자녀 주 양육자의 가족건강성이 사회적 지지와 행복감 사이에서 매개효과가 있는 것으로 나타났다. 연구결과를 바탕으로 하여 장애자녀 주양육자에 대한 사회적지지, 가족건강성, 행복감을 증진하기 위한 사회복지적 융복합적 제언을 제시하였다.

• 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.