• 제목/요약/키워드: Correlation of Burden

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한국 요양시설을 이용하는 직장인 가족의 노인 돌봄 부담감에 영향을 미치는 요인 (Factors Influcing Elderly Care Burden of A Working Family in Korean Nursing Facilities: A Convergence Approach)

  • 성경미;김은정
    • 디지털융복합연구
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    • 제18권2호
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    • pp.333-342
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    • 2020
  • 본 연구의 목적은 직장인을 대상으로 요양시설 노인의 돌봄 부담감을 조사하고 이에 영향을 미치는 특성들을 파악하는 것이다. 연구방법은 서술적 상관관계 연구로 5개 요양시설에 노인을 입소시킨 153명의 직장인 가족이었다. 자료는 2019년 7월부터 10월까지 자가보고형 설문지를 통해 수집하였다. 자료는 SPSS WIN 25.0 프로그램을 이용하여 독립표본 t-test, one-way ANOVA, Pearson's correlation, 그리고 hierarchical multiple regression으로 분석하였다. 연구결과 직장인 가족의 노인 돌봄 부담감에 유의하게 영향을 미치는 요인은 노인과의 관계, 요양비 부담정도, 요양시설 서비스에 대한 만족으로 나타났으며 이들의 설명력은 20.8%였다. 또한 직장인 가족의 노인 돌봄 부담감에 유의하게 영향을 미치는 개인의 특성들을 심리적, 사회적, 경제적 및 신체적 부담영역별로 확인하였으며 이러한 결과는 돌봄 가족의 부담감을 줄이기 위한 중재방안에 활용될 수 있다.

중환자실 입원 노인 중증도별 주 부양가족의 부담감 영향요인 비교 (A Comparative Study of the Factors Influencing Burden of Primary Family Caregivers according to the Degree of Serious Illness of Elderly Patients Admitted in an Intensive Care Unit)

  • 김귀분;한경숙;석소현
    • 성인간호학회지
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    • 제21권2호
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    • pp.187-198
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    • 2009
  • Purpose: This study was to compare and examine the factors influencing burden of primary family caregivers according to the severity of illness of elderly patients admitted in an intensive care unit. Methods: Subjects were the families of elderly patients in intensive care units of K, S and Y hospitals in Seoul. Data were collected from March to October 2007. Subjects were 108 persons over age 65. Data were analyzed by SAS statistics. Results: First, groups 5 and 3 showed higher burden than that of group 4. Second, high correlation was found between stress and burden, stress and anxiety, and burden and anxiety. Third, factors influencing family burden were found to be stress for group 5, stress, anxiety, and monthly income for group 4, and stress and patient age for group 3. Conclusion: Specific nursing interventions to decrease the stress of primary family caregivers of serious ill elderly patients in an intensive care unit are needed. Additionally, more effective and systematic activation of a long-term medical insurance system for seriously ill seniors is considered necessary to mediate the burden of primary family caregivers.

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치매노인을 돌보는 가족부양자 부양부담의 영향 요인: 치매지원센터 이용자를 중심으로 (Influencing Factors on Care Burden among Family Caregivers for Elders with Dementia: Focusing on Family Caregivers using a Support Center for Dementia)

  • 임경춘
    • 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.

An Efficient Signal Processing Scheme Using Signal Compression for Software GPS Receivers

  • Cho Deuk-Jae;Lim Deok-Won;Park Chan-Sik;Lee Sang-Jeong
    • International Journal of Control, Automation, and Systems
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    • 제4권3호
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    • pp.344-350
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    • 2006
  • The software GPS receivers based on the SDR technology provide the ability to easily adapt the other signal processing algorithms without changing or modifying the hardware of the GPS receiver. However, it is difficult to implement the software GPS receivers using a commercial processor because of the heavy computational burden for processing the GPS signals in real-time. This paper proposes an efficient GPS signal processing scheme to reduce the computational burden for processing the GPS signals in the software GPS receiver, which uses a fundamental notion compressing the replica signals and the encoded look-up table method to generate correlation values between GPS signals and replica signals. In this paper, it is explained that the computational burden of the proposed scheme is much smaller than that of the typical GPS signal processing scheme. Finally, the processing time of the proposed scheme is compared with that of the typical scheme, and the improvement in the aspect of the computational burden is also shown.

치매지원센터 간호사의 치매지식, 태도, 간호부담감 간의 상관관계 (Relationship among Dementia Knowledge, Attitude, and Care Burden of Nurses in Center for Dementia)

  • 고일선;한은경;김두리
    • 한국융합학회논문지
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    • 제8권9호
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    • pp.67-75
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    • 2017
  • 본 연구의 목적은 치매지원센터 간호사의 치매지식, 치매노인에 대한 태도, 간호부담감과의 관계를 분석하기 위함이다. 본 연구는 서술적 조사연구로 연구대상자는 서울시 25개 자치구의 치매지원센터에 근무하는 간호사 101명을 대상으로 하였으며, 구조화된 설문지로 자가설문조사를 수행하였다. 연구결과 치매지식은 20점 만점에서 평균 $18.14{\pm}1.09$점, 치매노인에 대한 태도는 266점 만점에 평균 $153.07{\pm}.76$점, 간호부담감은 64점 만점에 평균 $28.01{\pm}7.09$점이었다. 또한 치매지원센터 간호사의 치매지식이 높을수록 간호부담감이 낮았으며(r=-.32, p<.001), 치매노인에 대한 태도가 부정적일수록 간호부담감이 높았다(r=.25, p<.05). 추후 치매지원센터 간호사의 간호부담감을 줄이기 위해서는 치매지식을 높이고, 치매노인에 대한 태도를 긍정적으로 바꿀 수 있는 지속적인 교육과 정책적 지원이 필요하다.

암 환자 돌봄제공자의 돌봄부담감과 대처방식이 소진에 미치는 영향 (Influence of Caring Burden and the Way of Coping on Burnout in Caregivers of Cancer Patients)

  • 허수빈;신소영
    • 한국직업건강간호학회지
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    • 제28권2호
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    • pp.114-123
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    • 2019
  • Purpose: The aims of this study were to identify the effects of caring burden and the way of coping on burnout in caregivers of cancer patients. Methods: One-hundred and forty family caregivers of cancer patients who visited the cancer center at one tertiary hospital in metropolitan city B were included. The data collection was conducted from August 1st to October 1st, 2018, using a structured, self-reported questionnaire. The collected data were analyzed using descriptive statistics, t-test, one-way ANOVA, Pearson correlation coefficients, and multiple regression. Results: In the multiple regression analysis, the subject's gender (${\beta}=.12$, p=.028) and caring burden (${\beta}=.74$, p<.001) had a significant effect on burnout. The explanatory power of the subject's gender, education level, religion, caring time, number of family caregivers, monthly income, economic burden, expectation for treatment, caring burden, the way of aggressive coping, and the way of passive coping with burnout was 63.8% (F=23.28, p<.001). Conclusion: Reducing the caring burden in family caregivers of cancer patients will ultimately contribute to reducing burnout, thereby contributing to an improvement in the psychological well-being and quality of life of family members, as well as positively contributing to the recovery of patients.

뇌졸중 환자 가족 간호제공자의 불안과 부담감의 예측 요인: 자기효능과 돌봄에 대한 지식을 중심으로 (Sources of Anxiety and Burden of Family Caregivers of Stroke Patients: The Role of Self-efficacy and Knowledge about Care)

  • 김인자
    • 성인간호학회지
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    • 제24권1호
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    • pp.1-10
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    • 2012
  • Purpose: Among the sources of anxiety and burden of family caregivers of stroke patients, this study investigated the role of self-efficacy and knowledge about care. Methods: Descriptive and correlational study design was used. One hundred and thirteen subjects were included. They were anticipated family caregivers of stroke patients. All patients were hospitalized at the intensive care unit (ICU) for the first time as a stroke patients. Data of family caregivers were collected during the time that patients were in the ICU with self-reported standardized questionnaire. Pearson's correlation coefficients and regression analysis were used to explore the role of self-efficacy and knowledge. Results: Self-efficacy was correlated with burden, but not with anxiety. Knowledge about care was correlated with anxiety and burden. Only knowledge about care was the significant predictor of anxiety and burden of anticipated family caregivers. Conclusion: The knowledge about care for stroke patients is important especially to the family caregivers who have to care stroke patients for the first time to reduce their anxiety and burden.

노인 만성 질환자의 일상생활 수행정도와 가족간호자의 부담감 (Activities of Daily Living of The Elderly with a Chronic Disease and Burden on Family Care-givers)

  • 방수향;장희정
    • 대한간호학회지
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    • 제37권1호
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    • pp.135-144
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    • 2007
  • Propose: The purpose of this study was to help families decrease and alleviate the burden on family care-givers taking care of elderly patients. Method: Data was collected by a questionnaire from 100 family members who were registered in the department of home health care nursing at 4 hospitals of H University Medical Center from September 20 to October 25, 2005. The collected data was analyzed using Mean and Standard Deviation, Pearson Correlation Coefficient, t-test and One-Way ANOVA with the Duncan's test, and Stepwise multiple regression. Result: The average burden on family care-givers of elderly patients with chronic diseases was 3.31. The social burden was the highest(M=3.68), the lowest was the emotional burden(M=2.95). In ADL of elderly patients with chronic diseases, all 10 questions showed an average point above 2.50. The dependency level of going up and down the stairs was the highest(M=2.88). Conclusion: This research is necessary for the application of a plan in the social support system in order to reduce the burden on family care-givers who are taking care of elderly patients with a chronic disease.

일부 농촌 지역 치매노인 가족의 부양부담에 관한 연구 (A Study of the Family Caregiver's Burden for the Senile Dementia in a Rural Area)

  • 장인순
    • 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%).

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중환자실 입원환자 가족의 부담감과 요구도 (Burden and Needs of the Family Members of the Intensive Care Unit Patients)

  • 이지원;임선영
    • 한국콘텐츠학회논문지
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    • 제14권2호
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    • pp.421-429
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    • 2014
  • 본 연구는 가족의 중환자실 입원이라는 위기상황에 직면한 중환자실 입원환자 가족을 대상으로, 부담감과 요구도 정도 및 관계를 확인하여 중환자실 입원환자 가족을 위한 간호중재 개발의 기초자료를 마련하기 위하여 시도되었다. 연구대상은 2013년 5월부터 10월까지 B지역에 소재한 4개의 종합병원 중환자실에 입원한 환자의 가족 중 최소 입원기간이 3일이 경과한 환자의 가족 중 주간호대상자 93명을 대상으로 하였다. 자료 분석은 SPSS WIN 20.0 프로그램을 활용하여 t-test와 ANOVA, Scheff$\acute{e}$ test, Pearson's correlation coefficient로 분석 하였다. 연구 결과로 중환자실 입원환자 가족의 부담감은 평균 3.56점(5점 만점)로 중등도로, 요구도는 평균 3.58점(4점 만점)으로 높았으며, 일반적 특성 중 입원기간에 따라 부담감에 유의한 차이(F=3.463, p=.036)가 있었다. 또 부담감과 요구도의 관계는 유의한 순상관관계(r=.332, p<.001)로 나타났다. 이상의 결과를 볼 때 중환자실 입원환자 가족의 부담감을 감소시키고 요구도를 만족시키기 위한 적극적인 간호중재가 이루어질 때 가족의 위기는 완화되고 나아가 환자의 회복에도 긍정적인 영향을 미칠 수 있을 것으로 사료된다.