Please use this identifier to cite or link to this item: https://ah.lib.nccu.edu.tw/handle/140.119/73320
題名: 時間與空間的另類喘息:家庭照顧者使用支持性方案之經驗
Alternative Respite in Time and Space: Caregivers` Experience in Using Supportive Programs
作者: 蔡曉欣
Tsai, Hsiao Hsin
貢獻者: 呂寶靜
蔡曉欣
Tsai, Hsiao Hsin
關鍵詞: 家庭照顧者
支持性方案
喘息服務
自助團體
Family caregiver
supportive program
respite care
self-help group
日期: 2013
上傳時間: 3-二月-2015
摘要: 家庭照顧者的照顧負荷沉重,其多表達有支持性服務的需要,故針對家庭照顧者使用支持性方案之經驗,頗值得研究加以探討。本研究目的為瞭解家庭照顧者使用支持性方案的情形為何,進而探索使用服務期間從事活動的經驗,剖析家庭照顧者在使用支持性服務期間重新回復能量之過程。\n本文採質性研究法,以深度訪談法蒐集資料,訪談樣本來自台灣失智症協會,共有4位失智症照顧者接受訪談。主要研究結果如下﹕\n1.家屬使用「各項家庭照顧者支持性方案」的情形,以瑞智學堂、瑞智互助家庭、家屬聯誼會為例,進而比較上述三項服務方案之異同:(1)學堂到互助家庭,家屬「聚在一起」和「舒緩的時間」更多;家屬更懂得「釋放關心」。(2)從學堂到家屬聯誼會:「家屬未經組織的團體聚會」到「成為團體成員後的聚會」。(3)服務對象與受惠對象方面,學堂服務對象以「失智長者為主,長者受惠較多」;互助家庭以「長者和家屬為主,家屬受惠較多」;家屬聯誼會以「家屬為主,家屬受惠較多」;但其實「長者與家屬之間具有相互性」,家屬獲益之後,更能以健康的身心靈來提供長者的照顧,相對的,長者的功能得以維持或減緩退化,亦有益於家屬提供照顧。\n2.家屬的需求與動力是推動支持性方案重要的推展,從學堂到互助家庭的歷程,家屬與長者有三個階段的活動經驗,包含麻將班、烹飪班以及樂樂班,其顯示家屬有時間、空間以及活動參與的需求。\n3.家屬使用服務期間從事活動獲得「心理喘息」的要素,可就休閒與休息、自我效能感、團體的歸屬感、採取行動的層面進行分析,分別為(1)休閒與休息:「才能展現」、「享受說話」以及提升生活「滿意感」;(2)自我效能感:「學習」、「突破」、「成就感」的過程,增進自我效能感;(3)團體的「歸屬感」,以及(4)社會貢獻的使命和生命的「意義感」,可見家屬由照顧者蛻變成助人者的軌跡。
The caregivers in families carry a heavy responsibility, and many of them express the need for supportive services. As such, their experience in using supportive programs warrants further study and examination. In this study, we aim to first understand how such programs are being used. Next, we examine the restorative process in which caregivers use such services to gain respite.\nThis study used the qualitative research approach, and collected data from Taiwan Alzheimer`s Disease Association and included semi-structured in-depth interviews with four caregivers of the elderly with dementia. The research findings were listed below:\n1.We studied the following three supportive programs and analyzed their similarities and differences: the School of Wisdom, the Family of Wisdom, and the Family Club. (1) As the group progresses from the School of Wisdom to the Family of Wisdom, family members have more and more time to spend together and respite time; they also tend to show more care for others. (2) As the group progresses from the School of Wisdom to the Family Club, unorganized group gatherings evolve into organized gatherings for members of the group. (3) The target participants for the School, the Family and the Club are, respectively, senile seniors, seniors and their families, and families; the beneficiaries of the programs are seniors, families, and families. However, there is also an interrelation between seniors and their families: families who benefit from improved mental, physical and spiritual health are better able to care for their seniors. Vice versa, it is easier for families to care for seniors who are able to maintain or mitigate the degeneration of their daily functions.\n2.The needs and motivations of families are pivotal drivers for supportive programs. Throughout the evolution from the "School" to the "Family", families and seniors go through three stages of participation in activities, namely, mahjong classes, cooking classes and hobby classes. The progress reveals the families` need for respite time and space and their levels of participation. \n3.Families enjoy a restorative mental break by participating in activities. We analyzed the key elements of this mental break: leisure and rest, self-efficacy, belongingness, and level of participation. (1) Leisure and rest: display of talent, enjoyment of talking, and enhanced satisfaction toward life. (2) Self-efficacy: enhanced self-efficacy through the process of learning, breakthrough and sense of achievement. (3) Belongingness: the sense of belonging to a group. (4) Level of participation: the sense of mission to contribute to the society and meaning of life demonstrated by the families show an evolution from being the caregiver to the one who helps others.
參考文獻: 一、中文部分\n中華民國家庭照顧者關懷總會(2012)。長期照顧壓力大 家總:應增加服務預算 給家庭照顧者周休喘息服務。上網日期:2013年06月15日,檢自: http://www.coolloud.org.tw/node/71550。\n內政部統計資料(2008)。老人狀況調查摘要分析。上網日期:2013年10月04日,檢自:http://sowf.moi.gov.tw/stat/Survey/list.html。\n王仕圖、吳慧敏(2003)。深度訪談與案例演練。於齊力、林本炫編,質性研究方法與資料分析。嘉義:南華教社所。\n王增勇(2008)校閱序:質性研究不只是一種方法,更是一種生活態度。於陳秋山、王玉馨譯(2008)社工質性研究。台北:華都。Ian Shaw & Nick Gould (2001)Qualitative research in social work. London: Sage.\n王增勇、蔡曉欣(2014)。自助互助做為另類助人服務類型:以瑞智互助家庭為例。社區發展季刊,145,218-231。\n王麗雪、何美瑤、呂桂雲、葉淑惠(2007)。照顧者社會支持、照顧評價和失能老人家庭照顧品質的相關性探討。實證護理,3(3),177-187。\n行政院衛生署(2012)。長照十年計畫成果。上網日期:2013年10月04日,檢自:http://search.mohw.gov.tw/TSSearch/SearchResult?Keyword=%E9%95%B7%E7%85%A7%E5%8D%81%E5%B9%B4%E8%A8%88%E7%95%AB%E6%88%90%E6%9E%9C&searchTemplate=4。\n吳淑瓊(2005)。人口老化與長期照護政策。國家發展季刊,4,5-24。\n呂寶靜(2001)。「第六章 支持家庭照顧者之福利政策建構」,老人照顧:老人、家庭、正式服務。台北:五南。\n呂寶靜(2001)。「第四章 老人日間照護方案功能之初探:老人福利?喘息照顧?」,老人照顧:老人、家庭、正式服務。台北:五南。\n呂寶靜(2005)。支持家庭照顧者的長期照護政策之構思。國家政策季刊,4,25-40。\n呂寶靜(2012)。老人福利服務。台北:五南。\n宋麗玉(2006)。增強權能量表之發展與驗證。社會政策與社會工作學刊,10(2),49-86。\n宋麗玉(2008)。增強權能策略與方法:台灣本土經驗之探索。社會政策與社會工作學刊,12(2),123-194。\n李政賢譯(2006)。質性研究:設計與計畫撰寫。台北:五南。\n李玲(1997)。精神病患家屬參與自助團體主觀經驗之探究-以台北市心理復健家屬聯合協會為例。東吳大學社會工作研究所碩士論文。台北:東吳。\n李淑霞、吳淑瓊(1998)。家庭照顧者負荷與憂鬱之影響。護理研究,6(1),57-68。\n杜怡君(2011)。以壓力歷程模式探討女性失智症家庭照顧者其正向照顧經驗、因應模式及睡眠之相關研究。天主教輔仁大學臨床心理學系碩士班碩士論文。台北:輔仁。\n周月清、鄒平儀(2004).成年心智障礙者及其主要照顧者使用臨托服務影響之研究.社會政策與社會工作學刊,8(2),39-82。\n社團法人台灣失智症協會(2014)。瑞智學堂。上網日期:2014年02月08日,檢自:http://www.tada2002.org.tw/sow.tada2002.org.tw/sow_ideal.html。\n邱啓潤、許淑敏、吳淑如(2003)。居家照護病患之主要照顧者綜合性需求調查。醫護科技學刊,5(1),12-25。\n邱啟潤、許淑敏、吳瓊滿(2002)。主要照顧者負荷、壓力與因應之國內研究文獻回顧。醫護科技學刊,4(4),273-290。\n秦燕(2002)。老人照顧者自助團體的組織與運作研究。社區關懷與老人保健研討會論文集,249-275。\n張宏哲 審閱(2007)。人類行為與社會環境。林哲立、邱曉君、顏菲麗(合譯)。Ashford, J. B. & LeCroy, C. W. & Lortie, K. L著(2001)。台北:雙葉。\n陳向明(2002)。社會科學質的研究。台北:五南。\n陳芬婷(2011)。家庭照顧者使用喘息服務之成效及其相關因素探討。高雄醫學大學護理學研究所學位論文。高雄:高雄醫學大學。\n陳美妙、陳品玲、陳靜敏、徐亞瑛(2005)。機構是喘息服務對失能老人主要照顧者負荷之影響。長庚護理,16,152-166。\n陳翠芳、黃璉華(2010)。台灣地區居家式喘息服務的效益及影響效益的因素。護理研究期刊,18,18-25。\n喘息服務操作手冊(1999)。台北:中華民國現代社會福利總會。\n曾華源、白倩如(2012)。團體動力、體驗學習與社會團體工作。社區發展季刊,140,5-17。\n曾華源、鄭夙芬、溫信學 編著(2013)。社會團體工作。新北市:空大。\n湯麗玉、吳沛錡、李會珍、洪心平(2013)。瑞智互助家庭-失智症共同居家照護方案。長期照護雜誌,17(1),1-9。\n馮譯葶(2011)。走出生命負荷、發掘成長能量-家庭照顧者參與自助團體經驗之初探。國立政治大學社會工作研究所碩士論文。台北:政大。\n黃秀梨、張媚、余玉眉(2006)。我國機構式喘息服務政策之分析與建言。護理雜誌,53(2),59-66。\n黃秀梨、陳月枝、熊秉荃(2006)。從社會批判理論角度看台灣的喘息服務。護理雜誌,53(1),72-79。\n黃惠玲、徐亞瑛、黃秀梨、陳獻宗(2008)。失智症照顧服務之可行模式。研考雙月刊,32(6),22-33。\n楊明理(2011)。淺談賦能概念在喘息服務之應用。台灣心理諮商季刊,3(1),16-28。\n楊明理(2011)。喘息服務對家庭照顧者之賦能歷程研究。暨南大學輔導與諮商研究所學位論文。南投:暨大。\n鄒川雄(2003)。生活世界與默會知識:詮釋學觀點的質性研究。於齊力、林本炫(編)質性研究方法與資料分析。嘉義:南華社教所。\n潘淑滿(2003)。質性研究理論與應用。台北:心理。\n蔡啟源(2009)。老人喘息服務之探討。社區發展季刊,128,297-312。\n衛生福利部(2013)。失智症防治照護政策綱領。上網日期:2014年06月28日,檢自:http://www.mohw.gov.tw/cht/DONAHC/DM1_P.aspx?f_list_no=716&fod_list_no=0&doc_no=31602\n衛生福利部(2013)。長期照顧服務網計畫(第一期)-102年至105年。上網日期:2014年06月28日,檢自:http://www.ey.gov.tw/News_Content.aspx?n=7084F4E88F1E9A4F&sms=114AAE178CD95D4C&s=2B1578C89676E7DC\n鄭秀容、曾月霞(2008)。居家失智老人家屬照顧者照顧需求及需求被滿足情形之研究。榮總護理,25(4),386-392。\n二、西文部分\nArai, Y., Kumamoto, K., Washio, M., Ueda, M., Miura, H., & Kudo, K. (2004). Factors related to feelings of burden among caregivers looking after impaired elderly in Japan under the long-term care insurance system. Psychiatry and Clinical Neurosciences, 58, 396-402.\nAshworth, M. & Baker, A. H. (2000).‘Time and space’: carers’ views about respite care .Blackwell Science Ltd, Health and Social Care in the Community, 8(1), 50-56.\nBorkman, T. (2010). Conceptualizing Self-Help/ Mutual Aid. Presentation at first organizing conference of Special Issue on Nordic Self-Help. September 2010, Norway.\nCannuscio , C. C., Colditz, G. A., Rimm, E. B., Berkman, L. F., Jones, C. P., & Kawachi, I. (2004). Employment status, social ties, and caregivers’ mental health. Social Science and Medicine, 58, 1247-1256.\nGaugler, J. E., Jarrott, S. E., Zarit, S. H., Stephens, M. P., Townsend, A., & Greene, R. (2003). Adult day service use and reductions in caregiving hours: Effects on stress and psychological well-being for dementia caregivers. International Journal of Geriatric Psychiatry, 18, 55-62.\nGottlieb,B.H. & Johnson, J. (2000). Respite programs for caregivers of persons with dementia: a review with practice implications. Aging & Mental Health, 4(2), 119-129. \nGreene, R. C., & Feinberg, L. F. (1999). State initiatives for caregivers of people with dementia. Generations, 23(3), 75-77.\nGreenwood﹐N.﹐Habibi﹐R. & Mackenzie﹐A. (2012). Respite: carers’ experiences and perceptions of respite at home. BMC Geriatrics﹐12(42), ISSN (online) 1471-2318. \nHilgeman, M. M., Durkin, D. W., Sun, F., DeCoster, J., Allen, R. S., Gallagher-Thompson, D., & Burgio, L. D. (2009). Testing a theoretical model of the stress process in Alzheimer`s caregivers with race as a moderator. Journal of Gerontologist, 49(2), 248-261.\nHodge, D. R. & Sun, F. (2012). Positive feeling of caregiving among Latino Alzheimer’s family caregivers:Understanding the role of spirituality. Aging & Mental Health, 16(6), 689-698. \nLosada, A., Perez-Penaranda, A., Rodriguez-Sanchez, E., Gomez-Marcos, M. A., Ballesteros-Rios, C., & Ramos-Carrera, I.R. (2010). Leisure and distress in caregiver for elderly patients. Archives of Gerontology and Geriatrics, 50, 347-350.\nLosada, A., Perez-Penaranda, A., Rodriguez-Sanchez, E., Gomez-Marcos, M. A., Ballesteros-Rios, C., & Ramos-Carrera, I.R. (2010). Leisure and distress in caregiver for elderly patients. Archives of Gerontology and Geriatrics, 50, 347-350.\nMausbach, B. T., Coon, D.W., Patterson, T. L., & Grant, I.(2008). Engagement in activities is associated with affective arousal in Alzheimer’s caregivers: A preliminary examination of the temporal relations between activity and affect. Behavior Therapy, 39, 366-374. \nMausbach, B. T., Patterson, T. L., & Grant, I. (2008). Is depression in Alzheimer's caregivers really due to activity restriction? A preliminary mediational test of the Activity Restriction Model. Journal of Behavior Therapy and Experimental Psychiatry, 39, 459-466.\nPearlin, L. I., Mullan, J. T., Semple, S. J., & Skaff, M. M. (1990). Caregiving and the stress process: An overview of concepts and their measures. Journal of The Gerontologist, 30(5), 583-591.\nSalin, S., Kaunonen, M., & Astedt-Kurki, P. (2009). Informal carers of older family members: How they manage and what support they receive from respite care. Journal of Clinical Nursing, 18, 492-501.\nSemiatin, A. M. & O’Conner, M. K.(2012). The relationship between self-efficacy and positive aspects of caregiving in Alzheimer’s disease caregivers. Aging & Mental Health, 16(6), 683-688.\nSpeer, P. W.(2000). Intrapersonal and interactional empowerment: Implications for theory. Journal of Community Psychology, 28(1), 51-61. \nStrang﹐V. R. (2001). Family caregiver respite and leisure: A feminist perspective. Scandinavian Journal of Caring Sciences﹐15(1)﹐74-81.\nSussman, T., & Regehr, C. (2009). The influence of community-based services on the burden of spouses caring for their partners with dementia. Health & Social Work, 34(1), 29-39.\nVictor E. (2009). A Systematic Review of Interventions for Carers in the UK: Outcomes and Explanatory Evidence. The Princess Royal Trust for Carer in association with Young Carer Internation and the University of Nottingham, 1-168. \nWaKui, T., & Saito, T., Agree, E. M., & Kai I. (2012). Effects on home, outside leisure, social, and peer activity on psychological health among Japanese family caregivers. Aging & Mental Health, 16(4), 500-506. \nWatts, J. H., & Teitelman, J. (2005). Achieving a restorative mental break for family caregivers of persons with Alzheimer’s disease. Australian Occupational Therapy Journal, 52, 282-292.\nZimmerman, M. A. (1995). Psychological empowerment: Issues and illustrations. American Journal of Community Psychology, 23(5), 581-599.
描述: 碩士
國立政治大學
社會工作研究所
100264003
102
資料來源: http://thesis.lib.nccu.edu.tw/record/#G1002640031
資料類型: thesis
Appears in Collections:學位論文

Files in This Item:
File SizeFormat
003101.pdf3.8 MBAdobe PDF2View/Open
Show full item record

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.