최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기성인간호학회지 = Korean Journal of Adult Nursing, v.24 no.1, 2012년, pp.1 - 10
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 f...
* AI 자동 식별 결과로 적합하지 않은 문장이 있을 수 있으니, 이용에 유의하시기 바랍니다.
핵심어 | 질문 | 논문에서 추출한 답변 |
---|---|---|
가족 간호제공자의 불안과 부담감의 원인을 탐색하여 접근하는것이 가족 뿐만 아니라 뇌졸중 환자들을 위해서도 매우 중요한 이유는 무엇인가? | 그런데 뇌졸중 생존자들의 주 간호제공자는 아직도 가족인 경우가 대부분이므로 가족 내 뇌졸중 환자의 발생은 가족들에게 커다란 불안과 부담감을 야기한다. 이러한 문제는 가족중심적인 우리나라에서 더욱 문제가 되는 것으로 보고되었다(Choi-Kwon et al., 2009). 가족들의 불안과 부담감은 가족들의 삶의 질에 영향을 미쳐 간호를 하는 가족 당사자들의 삶의 질을 저해할 뿐만 아니라 환자의 예후에도 좋지 않은 영향을 미치는 것으로 여러 연구에서 보고되었다(Suh et al., 2005). | |
가족 간호제공자의 불안과 부담감에 대한 환자 관련 요인은 무엇인가? | 그런데 지금까지 이루어진 가족 간호제공자의 불안과 부담감에 대한 연구를 살펴보면 불안과 부담감은 여러 요인에 의하여 발생하는 것으로 보고되었다. 환자 관련 요인으로는 진단명, 뇌졸중 정도, 재발 여부, 인지장애 정도, 의사소통장애, 우울 등이 보고되었다(Scazufca, Menezes, & Almeida, 2002). 가족 간호제공자의 관련요인으로는 성별(Wilz & Kalytta, 2008), 사회적 지지 여부(Chang, Brecht, & Carter, 2001)와 자신감(Molloy et al. | |
뇌졸중의 경우 자기간호 활동부터 다른 사람의 돌봄이 필수적인 이유는 무엇인가? | 또한 의학의 발전과 더불어 발병 후 생존가능성이 증가하여 뇌졸중 생존자들에 대한 치료와 간호가 더욱 중요해지고 있다. 특히 뇌졸중은 다른 질환과 달리 치료 후 대상자가 생존하더라도 사지마비, 의사소통 장애, 인지장애 등과 같은 문제를 야기하는데 이러한 문제들로 인하여 인간의 가장 기본적인 활동인 자기간호 활동부터 다른 사람의 돌봄이 필수적이다(Suh et al., 2005). |
Chang, B. L., Brecht, M. L., & Carter, P. A. (2001). Predictors of social support and caregiver outcomes. Women Health, 33 (1-2), 39-61.
Choi-Kwon, S., Mitchell, P. H., Veith, R., Teri, L., Buzaitis, A., Cain, K. C., et al. (2009). Comparing perceived burden for Korean and American informal caregivers of stroke survivors. Rehabilitation Nursing, 34 (4), 141-150.
Courts, N. F. (2000). Psychosocial adjustment of patients on home hemodialysis and their dialysis partners. Clinical Nursing Research, 9 (2), 177-190.
Dunn, L. B., Aouizerat, B. E., Cooper, B. A., Dodd, M., Lee, K., West, C., et al. (2011). Trajectories of anxiety in oncology patients and family caregivers during and after radiation therapy. European Journal of Oncology Nursing, 16 (1) 1-9.
Gallagher, D., Ni Mhaolain, A., Crosby, L., Ryan, D., Lacey, L., Coen, R. F., et al. (2011). Self-efficacy for managing dementia may protect against burden and depression in Alzheimer's caregivers. Aging and Mental Health, 15 (6), 663-670.
Gao, L. L., Ip, W. W., & Sun, K. (2011). Validation of the short form of the Chinese childbirth self-efficacy inventory in Mainland China. Research in Nursing & Health, 34 (1), 49-59.
Han, K. S., Kang, E. S., Kim, H. O., Yang, M. H., & Kim, S. Y. (2004). Effect of a family education program on the family burden of the stroke. Journal of Korean Academy of Psychyatric and Mental Health Nursing, 13 (1), 43-50.
Hoffmann, T., Worrall, L., Eames, S., & Ryan, A. (2010). Measuring outcomes in people who had a stroke and their carers: Can the telephoe be used? Topics in Stroke Rehabilitation, 17 (2), 119-127.
Kalra, L., Evans, A., Perez, I., Melbourn, A., Patel, A., Knapp, M., et al. (2004). Training carers of stroke patients: Randomised controlled trial. British Medical Journal, 328 (7448), 1099. http://www.bmj.com/content/328/7448/1099
Kim, J. T. (1978). The relationship between trait anxiety and social tendency: Focused on Spielberger's STAI. Unpublished master's thesis, Korea University, Seoul.
Kim, D. H. (1998). A study on the health state and burden of the chronic patient's family members. Unpublished master's thesis, Pusan National University, Busan.
Lee, Y. S. (1993). The family burden of chronically ill patients at hospital. Unpublished master's thesis, Seoul National University, Seoul.
Lee, H. S., Kim, D. K., & Kim, J. H. (2006). Stress in caregivers of demented people in Korea: A modification of Pearlin and colleagues' stress model. International Journal of Geriatric Psychiatry, 21 (8), 784-791.
Macdonald, P., Murray, J., Goddard, E., & Treasure, J. (2011). Carer's experience and perceived effects of a skills based training programme for families of people with eating disorders: A qualitative study. European Eating Disorder Review, 19 (6), 475-486.
Molloy, G. J., Johnston, M., Johnston, D. W., Pollard, B., Morrison, V., Bonetti, D., et al. (2008). Spousal caregiver confidence and recovery from ambulatory activity limitations in stroke survivors. Health Psychology, 27 (2), 286-290.
Montgomery, R. J., Gonyea, J., & Hooyman, N. (1985). Caregiving and the experience of subjective and objective burden. Family Relations, 34 , 19-26.
Oeu, Y. S. (1997). A study on the mental health of the stroke patients' family. Unpublished master's thesis, Ewha Womans University, Seoul.
Oh, H. S. (1993). Health promoting behaviors and quality of life of Korean women with arthritis. Journal of Korean Academy of Nursing, 23 (4), 617-630.
Paukert, A. L., Pettit, J. W., Kunik, M. E., Wilson, N., Novy, D. M., Rhoades, H. M., et al. (2010). The roles of social support and self-efficacy in physical health's impact on depressive and anxiety symptoms in older adults. Journal of Clinical Psychology Medicine Settings, 17 (4), 387-400.
Rigby, H., Gubitz, G., Eskes, G., Reidy, Y., Christian, C., Grover, V., et al. (2009). Caring for stroke survivors: Baseline and 1-year determinants of caregiver burden. International Journal of Stroke, 4 (3), 152-158.
Romero-Moreno, R., Losada, A., Mausbach, B. T., Marquez-Gonzalez, M., Patterson, T. L., & Lopez, J. (2011). Analysis of the moderating effect of self-efficacy domains in different points of the dementia caregiving process. Aging and Mental Health, 15 (2), 221-231.
Scazufca, M., Menezes, P. R., & Almeida, O. P. (2002). Caregiver burden in an elderly population with depression in Sao Paulo, Brazil. Social Psychiatry and Psychiatric Epidemiology, 37 (9), 416-422.
Sherer, M., Maddux, J. E., Mercandante, B., Prentice-Dunn, S., Jacobs, B., & Rogers, R. W. (1982). The self-efficacy scale: Construction and validation. Psychological Reports, 51 (2), 663-671.
Smith, J., Forster, A., & Young, J. (2004). A randomized trial to evaluate an education programme for patients and carers after stroke. Clinical Rehabilitation, 18 (7), 726-736.
Spielberger, C., Gorsuch, R., & Lushene, R. (1970). STAI manual for the state-trait anxiety inventory. Palo Alto, CA: Consulting Psychologists Press.
Suh, M., Kim, K., Kim, I., Cho, N., Choi, H., & Noh, S. (2005). Caregiver's burden, depression and support as predictors of post-stroke depression: A cross-sectional survey. International Journal of Nursing Studies, 42 , 611-618.
Van Den Wijngaart, M. A., Vernooij-Dassen, M. J., & Felling, A. J. (2007). The influence of stressors, appraisal and personal conditions on the burden of spousal caregivers of persons with dementia. Aging and Mental Health, 11 (6), 626-636.
Vincent, C., Desrosiers, J., Landreville, P., & Demers, L. (2009). Burden of caregivers of people with stroke: Evolution and predictors. Cerebrovascular Disease, 27 (5), 456-464.
Williams, V. P., Bishop-Fitzpatrick, L., Lane, J. D., Gwyther, L. P., Ballard, E. L., Vendittelli, A. P., et al. (2010). Video-based coping skills to reduce health risk and improve psychological and physical well-being in Alzheimer's disease family caregivers. Psychosomatic Medicine, 72 (9), 897-904.
Wilz, G., & Kalytta, T. (2008). Anxiety symptoms in spouses of stroke patients. Cerebrovascular Disease, 25 (4), 311-315.
Yip, Y. B., Sit, J. W., Fung, K. K., Wong, D. Y., Chong, S. Y., Chung, L. H., et al. (2007). Effects of a self-management arthritis programme with an added exercise component for osteoarthritic knee: Randomized controlled trial. Journal of Advanced Nursing, 59 (1), 20-28.
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.