• 제목/요약/키워드: Caregiver(s)

검색결과 420건 처리시간 0.025초

경도 알츠하이머 치매환자와 보호자를 위한 가정기반 다요인 활동 프로그램(Home-based Multi-component Activities Program: Home-MAP)의 효과 (Effect of Home-based Multi-Component Activity Program (Home-MAP) for mild Alzheimer's Disease Patients and Caregivers)

  • 황윤정;정원미;이동영
    • 보건의료산업학회지
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    • 제9권3호
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    • pp.255-266
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    • 2015
  • Objective : The aim of this study was to examine the effects of the Home-based Multi-component Activity Program (Home-MAP) for the maintenance activities of daily living (ADL) for patients with mild Alzheimer's disease (AD) and on caregiver burden for caregivers. Methods : Nine mild AD patients and family caregivers. The Home-MAP was performed 1d/wk, for a total of 10 times over 10 weeks. Results : After the 10 sessions, participants' motor and process skills scores on the AMPS were found to have significantly improved (p=.028 and p=.028, respectively). The BPSD frequency score on the R-MBPC was found to be significantly reduced (p=.017). The BPSD symptoms related to caregiver reaction score on the R-MBPC and distress score on the NPI-Q were significantly reduced (p=.039 and p=.018, respectively). Conclusions : The Home-MAP appears to have contributed to the improvement of patients' capabilities in performing in ADL, to a reduction of BPSD, and to a reduction of burden related to BPSD.

뇌졸중 환자를 돌보는 가족의 심리적 안녕감에 영향을 미치는 요인 (Influencing Factors that Affect the Psychological Well-being in Family Caregivers of Stroke Patients)

  • 김정희;김옥수
    • 대한간호학회지
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    • 제35권2호
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    • pp.399-406
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    • 2005
  • Purpose: The purpose of this study was to investigate the factors that affect the psychological well-being in family caregivers of stroke patients. Method: The General Health Perception, short form 36, Health Survey Questionaire was used to measure health perception. The Caregiving Mastery Scale was used to assess the mastery, while the Psychological General Well-Being Index was used to examine the level of well-being. Result: Subjective health, caregiving mastery, patient's ADL and caregiving duration influenced on caregiver's psychological well-being. Subjective health had effect on psychological well-being both directly and indirectly. Caregiving duration and patient's ADL had indirect effect on psychological well-being through caregiving mastery. Conclusion: It is need to develop a health program for the caregivers of stroke patient's and to provide nursing intervention to improve the caregiver's ability, thereby improving the well-being of the family caregivers.

삼척시 유아의 보호자 사회경제적 지위 및 구강보건행태에 따른 간식 섭취 실태의 관련성 (Relationship between Snack Consumption Patterns and Socio-Economic Status and Oral Health Behavior in Samcheok-Si Children)

  • 노희진;정미애
    • 한국콘텐츠학회논문지
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    • 제13권8호
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    • pp.250-257
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    • 2013
  • 본 연구는 삼척소재 유아의 보호자 사회경제적 지위와 구강보건행태에 따른 간식 섭취 실태를 조사하였다. 삼척소재 3개 유치원 148명의 유아 보호자에게 설문조사를 실시한 후 결과를 분석하였으며, 보호자 사회경제적 지위 및 구강보건행태와 유아의 간식섭취 실태의 관련성을 알아보기 위하여 카이제곱검정과 로지스틱회귀분석을 이용하여 분석하였다. 연구결과 당 포함 간식 섭취빈도와 보호자의 교육수준, 그리고 가정의 수입에서 의미 있는 관련성이 검토되었다(p<.05), 또한, 탄산(청량)음료 섭취와 보호자 연령, 가정 수입에 따른 차이가 검토되었다(p<.05). 유아의 간식섭취와 구강보건행태에서는 보호자가 칫솔질을 해주는지 여부와 과일섭취빈도에서 의미 있는 관련성이 발견되었다(p<.05). 유아 보호자 사회경제적 지위 및 구강보건행태와 유아의 간식섭취 실태의 관련성을 로지스틱회귀분석을 통해 살펴본 결과 과일섭취빈도는 보호자 교육수준이 낮을 때 더욱 높았다(2.98(CI:1.01-8.81)). 탄산음료 섭취빈도는 보호자의 연령이 20-29세 일 때(14.51(CI:1.20-176.08)) 가장 높은 것으로 조사되었다. 보상성 당 제공의 경우 보호자 교육수준이 낮을 때(0.18(CI:0.05-0.68) 적게 제공되는 것으로 검토되었다.

고용량 $^{131}I$ 투여환자 퇴원이후 환자 간병인과 환자 가옥의 피폭선량 측정 (Caregiver or Family Doses due to Discharged $^{131}I$ Administrated Patient from the Hospital)

  • 정규환;이현국;조운갑;이재기
    • 대한방사선기술학회지:방사선기술과학
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    • 제33권2호
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    • pp.149-154
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    • 2010
  • 고용량 방사성요오드 $^{131}I$ 투여환자의 퇴원 이후 환자 가족이나 간병인, 가옥에 대한 외부피폭 방사선량을 개인선량계인 OSL(Optically Stimulated Luminescence dosimeter) 선량계를 사용하여 평가하였다. 3.37~5.55 GBq(100~150 mCi)의 $^{131}I$을 투여한 환자가 2박3일 또는 3박4일의 입원 기간이 지난 후 요양을 위하여 가정으로 귀가 한 후부터 5일에서 8일 동안 간병을 담당한 사람이 피폭한 방사선량과 집안 내 주요 지점에서의 누적 공간방사선량인 주변선량을 OSL 선량계를 이용하여 측정하였다. 고용량 치료 환자의 가족이나 간병인, 집안내 주요 지점에서의 누적피폭방사선량은 1 mSv의 1/10 수준인 0.1 mSv 내외로 측정되어 원자력법에서 정하고 있는 일반인에 대한 선량한도를 초과하지 않는 것으로 평가되었다. 소수의 표본임에도 불구하고 환자 주변인에 대한 측정값의 표준편차가 0.087 mSv로 크지 않았음을 볼 때 모집단인 전체 환자가족의 피폭 방사선량도 표본집단의 결과와 큰 차이를 보이지 않을 것으로 유추할 수 있어 환자의 입원 치료기간을 현재보다 단축하는 방안을 추가로 검토하거나 연구할 필요가 있을 것으로 보인다.

몽골 지적장애아동 주양육자의 교육요구 (Educational Needs of Primary Caregivers of Children with Intellectual Disability in Mongolia)

  • 김진희;박서진;이은영
    • 한국융합학회논문지
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    • 제10권3호
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    • pp.319-334
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    • 2019
  • 이 연구는 몽골 지적장애아 주양육자의 교육요구를 확인하기 위하여 수행되었다. 자료는 2017년 10월 25일부터 11월 30일까지 150명의 지적장애아동의 주양육자를 대상으로 수집되었다. 설문지는 10개의 범주에 35개 문항으로 구성되었다. 주양육자의 평균 교육요구도는 $4.05{\pm}0.65$점이었다. 정보와 지식습득 범주에서의 건강관련 교육요구도가 가장 높았다($4.48{\pm}0.57$). 주양육자의 교육요구도는 월 소득수준(F=7.07, p<.001), 보조양육자의 유무(t=-2.70, p=.008), 돌봐야 하는 추가 장애아동 유무(t=2.02, p=.046), 장애아동 어머니의 직업 유무(F=3.87, p=.023), 장애아동의 중복장애 유무(t=-2.60, p=.010)에 따라 통계적으로 유의한 차이가 있었다. 본 연구결과는 몽골의 지적장애아동 주양육자 지원 프로그램 개발 시 기초자료로 활용될 수 있을 것이라 기대된다.

뇌졸중 환자의 가족 기능에 영향을 미치는 요인 분석 (A Study on the Influencing Factors in Family Functioning of Stroke Patients)

  • 조복희
    • 재활간호학회지
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    • 제1권1호
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    • pp.1-14
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    • 1998
  • The purpose of this study was to identify the factors affecting family functioning of stroke patients. A descriptive survey research was conducted in which 65 stroke patients and their primary caregivers were conveniently sampled. Data were collected from July to September, 1998 through interviewing using a structured questionnare. The measuring instruments used were Barthel Index by Mahoney and Barthel(15 items), Quality of Relationship Scale by Archbold and Stewart(15 Items), Role Stress of Caregiver Scale by Yang(14 items), Situational Definition Scale by Lee(9 items), Family Hardiness Index by McCubbin, McCubbin. and Thompson(20 items), and Family Adaptability Cohesion Evaluation Scale(FACES-III) by Olson, Portner, and Lavee(20 items). The obtained data were analyzed using percentage, t-test, ANOVA, Duncan test, and Pearson coefficients correlation by SAS/PC program. The results were as follows; 1. Role Stress of Caregiver was not severe and Quality of Relationship was moderate. The level of Situational Definition of primary caregivers was not high but Family Hardiness and Family Functioning were rather high. 2. The following relationships between research variables and demographic characteristics of the primary caregivers of stroke patients were significantly different; occupation of caregiver between Quality of Relationship, occupation of caregiver between Situational Definition, family type between Role Stress, caregiving duration between Family Hardiness, caregiving duration between Family Functioning, and hospitalization days between Family Functioning. 3. The correlations between research variables were as follows; There was positively correlated between patient's ADL and Quality of Relationship. The relationship of the patient's ADL between Role Stress was negatively correlated. Quality of Relationship between Situational Definition, Family Hardiness, and Family Functioning were significantly correlated. The correlation of Situational Definition between Family Hardiness, and Situational Definition between Family Functioning were very high. As a result of these findings, Quality of Relationship, Role Stress, Situational Definition. and Family Hardiness were useful variables for identifying Family Functioning of stroke patients. It is important for the rehabilitation nurse to be knowledgeable about family functioning of stroke patients to promote rehabilitation process.

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중환자실 입원환자 가족의 삶의 질 영향요인 (Factors Affecting Quality of Life in Family Caregivers of Patients in Intensive Care Units)

  • 공경미;부선주;이영진;안정아
    • 중환자간호학회지
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    • 제17권2호
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    • pp.12-24
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    • 2024
  • Purpose : This study aimed to identify factors influencing the quality of life of family caregivers of intensive care unit (ICU) patients. Methods : We conducted a study using a cross-sectional design. The study involved 109 family caregivers of ICU patients at a university-affiliated hospital in Gyeonggi-do, South Korea. Data were collected through self-report questionnaires between July 2020 and April 2021 and analyzed using descriptive statistics, independent t-tests, one-way ANOVA, Pearson's correlation coefficients, and multiple regression analysis. Results : The study revealed significant differences in quality of life based on economic status (F=11.63, p<.001), cohabitation with patients (t=-2.04, p=.044), sleep duration after patient's admission to the ICU (t=-2.48, p =.025), and subjective health status (F=30.06, p<.001). There were significant negative correlations observed between quality of life and post-traumatic stress symptoms (r=-.38, p<.001) as well as caregiver burden (r=-.46, p<.001). Factors affecting quality of life were subjective health status, economic status, and caregiver burden (adj. R2=0.52, F=15.64, p<.001). Conclusion : These findings underscore the need to develop and implement intervention programs tailored to the health conditions and economic status of family caregivers, with a focus on alleviating caregiver burden. Such initiatives are essential to ultimately improve the quality of life for family caregivers of ICU patients.

성인자녀의 노부모 부양분담정도와 부양에 따른 부담감 (Care Sharing and Care Burden for Old Parent)

  • 이윤정
    • 가정과삶의질연구
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    • 제13권4호
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    • pp.125-138
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    • 1995
  • The main purpose of this study is to observe correlation between caregiver's burden and care sharing and then to contribute to improve relationship between old parents and their adult children. The research samples were collected by structured questionnare and 507 samples were finnally selected. The data analysis was conducted by the method of frequency mean Pearson's correlation multiple regression The major findings were as follows: Care-sharing was made much in the case of this SES the oldest daughter-in-law living together with old parents and old parents' economic incapacity Caretiver's burden was serious in the case of living with old parents the oldest daughter-in-law and old parents' economic incapacity. And the correlation between care sharing and caregiver's burden was positive.

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A Study on the Oral Health Literacy and Related Factors of Mother's in Some Areas

  • Kim, Mi-Jeong;Lim, Cha-Young;Son, Ju-Lee
    • 치위생과학회지
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    • 제21권1호
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    • pp.52-62
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    • 2021
  • Background: This study aims to provide basic data for development of the level-based oral health care program depending on the mother's oral health literacy by finding out how mother's oral health literacy can effect on the preschool children's oral health and behavior. Methods: The survey was conducted on 192 mothers who have preschool children and the data were analyzed by t-test, ANOVA, multiple regression analysis to identify differences in verbal and functional oral health literacy. Results: The study showed statistical significance (p<0.05) in educational level depending on differences in verbal and functional oral health literacy by sociodemographic factor. In differences in verbal and functional literacy depending on experience of education for oral health behavior and oral health, statistical significance (p<0.05) was showed highly on verbal and functional literacy in the case that subjects have an experience of education for oral health and their children have not been experienced of oral illness. And when it comes to the case that subjects have experience of education for oral health within one to two years, statistical significance was showed highly on verbal literacy. It showed that verbal and functional oral health literacy effects to oral health care behavior of children judging from results that the higher level of mother's verbal oral health literacy, the higher score of children's oral health knowledge, attitude and behavior. Conclusion: It is necessary to develop the systematic program which is appropriate for characteristics of each oral period in childhood depending on level of primary caregiver's oral health literacy, and systematic education should be preceded to enhance the literacy of the caregiver. It is considered necessary to improve the oral health care of children by developing a manual for oral health care education to enhance primary caregiver's oral health literacy.

사회적 지지의 특성에 따른 뇌졸중 환자의 우울 (The Relationship between the Characteristics of Social Support and Post-Stroke Depression)

  • 김인자;서문자;김금순;조남옥
    • 재활간호학회지
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    • 제2권2호
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    • pp.206-214
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    • 1999
  • The effect s of social support on post-stroke depression were investigated. Social support was classified into three categories : primary caregiver's, significant other's, and professional support. And primary caregiver's and significant other's support were divided into their relation, living state (which means they living together or not), frequency which they met at, and perceived satisfaction about the support, respectively. Professional support was divided into number of professionals who take care of, frequency they met at, and perceived satisfaction. The subjects were 254 stroke patients who had been discharged and were taken follow-up care at the out patient department. The depression was measured using CES-D. Out of the primary caregiver's support, only relation and perceived satisfaction were identified to affect the post-stroke depression. The patients who primarily their spouse takes care of were less depressed than those who their adult children take care of. None of the significant other's support affects the post-stroke depression. Only perceived satisfaction of the professional support was found to affect the post-stroke depression. So it was found that the quality, not the amount, of care was important to post-stroke depression. These results also support the claim that the facilities and teaching programs for primary caregivers are necessary.

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