English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 45422/58598 (78%)
造訪人次 : 2514329      線上人數 : 218
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋
    請使用永久網址來引用或連結此文件: http://libir.tmu.edu.tw/handle/987654321/36498


    題名: 失智症照顧者支持團體之統合分析研究
    作者: 簡伶育
    貢獻者: 護理學研究所
    關鍵詞: 失智症 照顧者 支持團體 統合分析
    日期: 2010
    上傳時間: 2010-10-21 10:39:44 (UTC+8)
    摘要: 目的:評值支持團體對於失智症照顧者的成效,並探討支持團體研究的特徵對效果量的影響。
    樣本來源:廣泛蒐集西元1998至2009年間以英文發表之研究,電子資料庫包含Cochrane Library、Medline、PUBMED、PsycARTICLES、PsycINFO、ERIC、Ageline、CINAL及Psychology and Behavioral Sciences Collection。
    樣本選擇:支持團體包含相互支持團體、教育心理團體及教育訓練團體,針對失智症非專業照顧者成效評值之英文量性文獻,共篩選出30篇(真實驗與類實驗)控制試驗研究。成效指標為照顧者之心理健康、憂鬱、負荷及社會結果。
    資料登錄:由兩位評分者分別獨立進行文章篩選及資料登錄,登錄特徵包含方法特徵、介入特徵及參與者特徵,並進行研究的品質評估,檢視統合分析的結果是否受到研究品質的影響。
    結果:整體來說,支持團體對於照顧者之心理健康(Hedge’s g=-0.44;95%CI=-0.73,-0.15)、憂鬱(Hedge’s g=-0.40;95%CI=-0.72,-0.08)、負荷(Hedge’s g=-0.23;95%CI=-0.33,-0.13)或社會結果(Hedge’s g=0.40;95%CI=0.09,0.71)都有其正面且顯著的效果。有無使用理論、團體期程與總時數的不同會顯著影響心理健康及憂鬱效果量的大小;女性參與比例(為心理健康、憂鬱)、平均年齡(為社會結果)的顯著預測變項。支持團體特徵變項經組間的比較,在心理健康及憂鬱結果上有相似的發現:隨機抽樣方法、高品質研究、教育心理團體、有使用理論、團體大小6~10人、有使用團體手冊、團體期程≧8週且團體總時數≧16小時、有進行追蹤測量、中度失智症患者的照顧者、多專業背景領導者的特徵可獲得顯著且較高的改善效果;而在負荷結果上:教育訓練團體、團體期程≧8週且團體總時數<16小時的特徵可獲得顯著且較高的改善效果,其餘特徵與心理健康及憂鬱有一致性的結果。
    結論:支持團體對照顧者「心理健康」、「憂鬱」、「負荷」及「社會結果」是有助益的,可以作為未來臨床工作者及研究者進行介入時的參考指引。

    Objectives: To evaluate the efficacy of such intervention and identify characteristics associated with intervention efficacy.
    Data Sources: Nine peer reviewed databases including Cochrane Library, Medline, PUBMED, PsycARTICLES, PsycINFO, ERIC, Ageline, CINAL, and Psychology and Behavioral Sciences Collection, were searched for controlled trials, preferably randomized, published in English from 1998 to 2009 inclusive.
    Study Selection: Studies on dementia caregiver support groups including mutual support groups, psychoeducational groups, as well as education and training programs were included. Thirty (20 randomized and 10 nonrandomized) controlled trials from English quantitative journal literatures that met inclusion criteria were selected.
    Data Extraction: Two reviewers independently identified trials, reviewed relevant articles, extracted data and compiled tables of intervention and participant characteristics and results associated with intervention efficacy, appraised the methodological quality of the trials, and summarized results. The outcome indicators of intervention include caregiver’s psychological well-being, depression, burden, and social outcomes.
    Results: All in all, support groups have a positive and significant effect on psychological well-being (Hedge’s g = -0.44; 95%CI = -0.73, -0.15), depression (Hedge’s g = -0.40; 95%CI = -0.72, -0.08), burden (Hedge’s g = -0.23; 95%CI = -0.33, -0.13), and social outcomes (Hedge’s g = 0.40; 95%CI = 0.09, 0.71) of dementia caregivers. The effects of psychological well-being and depression is significantly influenced by different factors, including theories, and duration and intensity in support groups. The proportion of female participant is an obvious predictor for psychological well-being and depression, while mean age predicts social outcomes. By comparing the characteristics of support groups, our analysis indicated that psychological well-being and depression of caregivers benefit significantly under the condition of random sampling, high quality research, psychoeducational groups, the use of theories and manual, the group size limitation of six to ten members, intensity and duration of no less than 16 hours and lasting longer than 8 weeks of the support group, patients with moderate dementia, and the leader with interdisciplinary background. On the other hand, support groups can also have a greater and obvious effect on caregivers’ burden under the condition of education and training programs, intensity and duration of no more than 16 hours and lasting more than 8 weeks of the support group. Other characteristics have identical influences on psychological well-being and depression of caregivers.
    Conclusions: Support groups are beneficial to caregivers of dementia patients in terms of psychological well-being, depression, burden and social outcomes. Our result provides future clinical workers and researchers with a useful reference.
    關聯: 167頁
    描述: (一)論文目次
    目 錄
    頁 數
    致 謝 ............................................ Ⅰ
    中文摘要 ............................................ Ⅲ
    英文摘要 ............................................ Ⅴ
    目 錄 ............................................ Ⅶ
    圖表目次 ............................................ Ⅹ

    第一章 緒論 .......................................... 1
    第一節 研究背景與動機 ............................. 1
    第二節 研究目的 ................................... 7
    第三節 研究問題 ................................... 8
    第二章 文獻探討 ...................................... 9
    第一節 失智症照顧者之衝擊 ......................... 9
    第二節 支持團體 ................................... 14
    第三節 影響失智症照顧者支持團體成效之因子 ......... 19
    第四節 失智症照顧者支持團體之成效 ................. 28
    第五節 統合分析 ................................... 33
    第三章 研究方法 ...................................... 45
    第一節 研究流程 ................................... 45
    第二節 統合分析研究樣本的選擇 ..................... 47
    第三節 研究工具 ................................... 54
    第四節 研究品質評估 ............................... 54
    第五節 每篇研究的重要特徵變項之登錄及研究架構 ..... 57
    第六節 評分及登錄者間信度 ......................... 61
    第七節 效果量的計算 ............................... 62
    第八節 單一研究的多重效果量 ....................... 65
    第九節 資料分析 ................................... 66
    第四章 分析與結果 .................................... 69
    第一節 研究樣本特徵分析 ........................... 69
    第二節 支持團體效果量之整體分析 ................... 74
    第三節 心理健康效果量與支持團體特徵分析 ........... 77
    第四節 憂鬱效果量與支持團體特徵分析 ............... 82
    第五節 負荷效果量與支持團體特徵分析 ............... 87
    第六節 社會結果效果量與支持團體特徵分析 ........... 92
    第五章 討論 .......................................... 94
    第一節 支持團體介入對失智症照顧者的整體效果 ....... 94
    第二節 方法特徵對心理健康、憂鬱、負荷效果的影響 ... 96
    第三節 介入特徵對心理健康、憂鬱、負荷效果的影響 ... 97
    第四節 參與者特徵對心理健康、憂鬱、負荷、社會結果效
    果的影響 .................................. 101
    第五節 研究特色與貢獻 ............................ 102
    第六章 結論、限制與建議 ............................. 105
    第一節 結論 ...................................... 105
    第二節 研究限制 .................................. 107
    第三節 未來研究與建議 ............................ 110

    參考資料
    中文部分 ....................................... 114
    英文部分 ....................................... 118

    附件
    附件一Characteristics of Included Studies (n=30). 146

    (二)參考文獻
    中文部份
    中華民國家庭照顧者關懷總會(2003)‧家庭照顧者支持團體緣起與發展‧於中華民國家庭照顧者關懷總會總校閱,家庭照顧者支持團體領導者手冊(1-4頁)‧台北:中華民國家庭照顧者關懷總會。
    內政部社會司(2007,8月9日)‧近年我國老人人口數一覽表‧2008 年6 月15 日,取自http://www.moi.gov.tw/stat
    王玉女、徐亞瑛、姚開屏、吳淑瓊(1998)‧失能老人家庭尋找平衡點的照顧過程及相關因素探討‧護理研究,6(6),489-500。
    王秀紅(1999)‧統合分析的概念及其在護理的應用‧護理研究,7(2),183-192。
    史曉寧、黃愛娟(1996)‧家庭重病老年患者之主要照顧者壓力源和其家庭功能因素之探討‧榮總護理,13(2),138-146。
    台灣失智症協會(無日期)‧失智症照護‧2008年8月28日取自http://www.tada2002.org.tw/index_news.php?ncid=3&nc2id=27
    白璐(2003)‧實症護理之統合分析‧護理雜誌,50(1),15-20。
    呂寶靜(2001)‧「老人照顧:老人、家庭、正式服務」‧台北:五南。
    李玉嬋(2008)‧支持團體在促進糖尿病健康自我管理的運用‧諮商與輔導,266,51-58。
    李永怡(2007)‧台灣青少年性行為介入計劃成效之統合分析研究‧未發表碩士論文,國立成功大學,台南。
    李娟娟(2003)‧失智症家屬支持團體之關注主題與成效探討‧未發表碩士論文,國立台北護理學院,台北。
    李英芬、蔡麗雲、張澤芸(2008)‧末期癌症病人之主要照顧者的負荷相關因素探討,安寧療護,13(4),394-410。
    吳淑瓊、林慧生(1999)‧台灣功能障礙老人家庭照護者的全國概況剖析‧中華公共衛生雜誌,18(1),44-53。
    官蔚菁(2004)‧台灣健康信念模式研究之統合分析究‧未發表碩士論文,國立成功大學,台南。
    邱啟潤、許淑敏(2000)‧談關懷家庭照顧者‧高雄護理雜誌,17(1),7-13。
    邱啟潤、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。
    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。
    邱啟潤、楊美賞、陳彰惠(2004)‧長期照護的遠景-以家庭為中心的老人照護‧長期照護雜誌,7(4),386-398。
    邱逸榛、黃舒萱、徐亞瑛(2004)‧阿滋海默氏患者照顧者之疲憊、負荷與憂鬱之間的關係‧長期照護雜誌,7(4),338-351。
    徐亞瑛(2000)‧支持團體對失智症家屬之助益‧應用心理研究,8,33-35。
    高淑芳、盧孳豔、葉淑惠、劉雪娥(1999)‧探討家庭功能社會支持與殘病老人照顧者負荷之關係‧護理研究,7(2),172-182。
    連啟舜(2002)‧國內閱讀理解教學研究成效之統合分析‧未發表碩士論文,國立台灣師範大學,台北。
    許淑敏、邱啟潤(2003)‧家庭照顧者的壓力源與因應行為:以一個支持團體為例‧護理雜誌,50(5),47-55。
    陳永慶(2001)‧國內心理治療與諮商輔導效果的整合分析研究‧未發表的碩士論文,高雄醫學大學,高雄。
    陳達夫、邱銘章、湯麗玉、林忠蔚、史宛玉、陳榮基(無日期)‧失智症盛行率調查報告‧2008年08月28日,取自http://www.tds.org.
    tw/html/front/bin/ptdetail.phtml?Part=022&Category =121256
    黃惠玲、徐亞瑛(2003)‧照顧者訓練方案對改善失智症照顧者能力之探討‧長期照護雜誌,7(2),121-134。
    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。
    黃寶園(2006)‧統合分析法‧於黃寶園總校閱,心理與教育研究法(一版,382-426頁)‧台北:華立。
    湯麗玉、毛家舲、周照芳、陳榮基、劉芳枝(1992)‧痴呆症老人照顧者的負荷及其相關因素探討‧護理雜誌,39(3),89-98。
    湯麗玉、葉炳強、陳良娟、謝碧容(2000)‧失智症家屬支持團體成效初探‧應用心理研究,7,171-190。
    葉炳強(1993)‧台灣地區的老年期癡呆人口有多少?健康教育,72,10-15。
    葉柄強、楊清姿(1994)‧癡呆症患者及家庭之居家照護經驗‧行政院衛生署83年度委託研究計畫醫療保健工作研究報告。
    劉淑言、吳聖良、蘇東平、周桂如(2002)‧精神分裂症病患主要照顧者支持團體成效之評值‧護理雜誌, 49(4),31-41。
    蕭勝煌(2008,5月1日)‧臺北市立聯合醫院仁愛院區「仁愛心、失智情」55週年院慶系列活動新聞稿‧2008年8月28日,取自http://www.health.gov.tw/Default.aspx? tabid =36 &mid=442&item-id=20543
    應立志、鍾燕宜(2000)‧整合分析方法與應用‧台北:華泰。
    謝素真、黎士鳴、毛鳳雪、鄒慧韞‧探討支持團體對新進護理人員身心健康之成效‧童綜合醫誌,3 ( 1 ),20-26。
    謝耀文、高東偉、黃宗正(2005)‧老年憂鬱症‧長期照護雜誌,10 ( 3 ), 207-215。
    英文部分
    加有星標符號(*)的參考文獻為本研究統合分析的研究樣本。
    Acton, G. J., & Kang, J. (2001). Interventions to reduce the burden of caregiving for an adult with dementia: A meta-analysis. Research in Nursing & Health, 24(5), 349-360.
    Almberg, B., Jannson, W., Grafstorm, M., & Winblad, M. (1998). Differences between and within genders in caregiving strain: a comparison between caregivers of demented and non-caregivers of non-demented elderly people. Journal of Advanced Nursing, 28(4), 849-858.
    Alzheimer's Disease International(ADI). (2005, MAY 19). Help for carers. Retrieved August 28, 2008, from http://www.alz.co.uk/ carers.
    *Andrén, S., & Elmståhl, S. (2008a). Effective psychosocial intervention for family caregivers lengthens time elapsed before nursing home placement of individuals with dementia: a five-year follow-up study. International Psychogeriatrics, 20(6), 1177-1192.
    *Andrén, S., & Elmståhl, S. (2008b). Psychosocial intervention for family caregivers of people with dementia reduces caregiver's burden: development and effect after 6 and 12 months. Scandinavian Journal of Caring Sciences. 22(1), 98-109.
    Aneshensel, C. S., Pearlin, L. I., Mullan, J. T., Zarit, S. H., & Whitlatch, C. J. (1995). Profiles in caregiving: The unexpected career. San Diego: Academic Press, Inc.
    Barclay, L. L., Zemcov, A., Blass, J. P., & Sansone, J. (1985). Survival in Alzheimer's disease and vascular dementias. Neurology, 35(6), 834-840.
    Beeson, R., Horton-Deutsch, S., Farran, C., & Neundorfer, M. (2000). Loneliness and depression in caregivers of persons with Alzheimer’s disease or related disorders. Issues in Mental Health Nursing, 21(8), 779-806.
    *Berger, G., Bernhardt, T., Schramm, U., Muller, R., Landsiedel-Anders, S., Peters, J., et al. (2004). No effects of a combination of caregivers support group and memory training/music therapy in dementia patients from a memory clinic population. International Journal of Geriatric Psychiatry, 19, 223-231.
    Biegel, D. E., & Schulz, R. (1999). Caregiving and caregiver interventions in aging and mental illness. Family Relations, 48(4), 345-354.
    Borenstein, M., Hedges, L., Higgins, J., & Rothstein, H. R. (2005). Comprehensive Meta Analysis, Version 2. Englewood, NJ: Biostat, Inc.
    Borenstein, M., Hedges, L., Higgins, J., & Rothstein, H. R. (2009). Introduction to Meta-Analysis. Chichester, UK: Wiley.
    Bourgeois, M. S., & Schulz, R. (1996). Interventions for caregivers of patients with Alzheimer’s disease: Areview and analysis of content, process, and outcomes. International Journal Aging and Human Development, 43(1), 35-92.
    Buckwalter, K. C., Gerdner, L., Kohout, F., Hall, G. R., Kelly, A., Richards, B., et al. (1999). A nursing intervention to decrease depression in family caregivers of persons with dementia. Archives of Psychiatric Nursing , 13(2), 80-88.
    Brodaty, H., Green, A., & Koschera, A. (2003). Meta-analysis of psychosocial interventions for caregivers of people with dementia. Journal of the American Geriatrics Society, 51(5), 657-664.
    Brogna, L. (1998). Caring for caregivers: Home care nursing's challenge. In J. A. Allender & C. L. Rector (eds.). Readings in gerontological nursing (pp. 515-522). Philadelphia: Lippincott.
    Burks, V. K. (1991). Dementia victim caregivers who participate or do not participate in support group services. Unpublished doctoral dissertation, University of Utah, Salt Lake.
    *Chien, W. T., & Lee, Y. M. (2008). A disease management program for families of persons in Hong Kong with dementia. Psychiatric Services, 59(4), 433-436.
    Chien, W. T., Chan, S., Morrissey, J., & Thompson, D. (2005). Effectiveness of a mutual support group for families of patients with schizophrenia. The Journal of Advanced Nursing, 51(6), 595-608.
    Chiverton, P., & Caine, E. D. (1989). Education to assist spouses in coping with Alzheimer’s Disease. Journal of the American Geriatrics Society, 37, 593-598.
    Chou, K. R. (1998). Caregiver burden: Structural equation modeling. Nursing Research, 6(5), 358-370.
    Chou, K. R. (2006). Support groups for caregivers of relatives with mental illness. New Taipei Journal of Nursing, 8(2), 1-10.
    Chou, K. R., Chyun, L. J., & Chu, H. (2002). The realiability and validity of the Chinese version of the aregiver burden inventory. Nursing Research, 51(5), 324-331.
    Chou, K. R., LaMonagne, L. L., & Hepworth, J. T. (1999). Burden experienced by caregivers of relatives with dementia in Taiwan. Nursing Research, 48(4), 206-214.
    Clark, P. C. (2002). Effect of individual and family hardiness on caregiver depression and fatigue. Research in Nursing and Health, 25, 37-48.
    Clipp, E. C., & George, L. K. (1990). Psychotropic drug use among caregivers of patients with dementia. Journal of the American Geriatrics Society, 38(3), 227-235.
    Cohen, J. (1988). Statistical power analysis for the behavioral sciences. NJ: Lawrence Erlbaum.
    Cooke, D. D., McNally, L., Mulligan, K. T., Harrison, M. J. G., & Newman, S. P. (2001). Psychosocial interventions for caregivers of people with dementia: a systematic review. Aging and Mental Health, 5(2), 120-135.
    *Coon, D. W., Thompson, L., Steffen, A., Sorocco, K., & Gallagher-Thompson, D. (2003). Anger and depression management: psychoeducational skill training interventions for women caregivers of a relative with dementia. Gerontologist, 43(5), 678-689.
    Cooper, H. M. (1989). Integrating research: A guide for literature reviews(2nd ed.). Newbury Park, CA: Sage.
    Cooper, H. M. (2010). Research synthesis and Meta-analysis. Thousand Oaks, CA: Sage.
    Cuijpers, P. (2005). Depressive disorders in caregivers of dementia patients: a systematic review. Aging & Mental Health, 9(4), 325-330.
    Dersimonian, R., & Laird, N.(1986). Meta-analysis in clinical trials. Control Clinical Trials, 7, 177-188.
    Dillehay, R. C., & Sandys, M. R. (1990). Caregivers for Alzheimer’s patients: what we are learning from research. International Journal of Aging and Human Development, 30, 263-285.
    *Done, D. J., & Thomas, J. A. (2001). Training in communication skills for informal carers of people suffering from dementia: a cluster randomized clinical trial comparing a therapist led workshop and a booklet. International Journal of Geriatric Psychiatry, 16, 816-821.
    *Droes, R. M., Breebaart, E., Meiland, F. J., Van Tilburg, W., & Mellenbergh, G. J. (2004). Effect of Meeting Centres Support Program on feelings of competence of family carers and delay of institutionalization of people with dementia. Aging and Mental Health, 8(3), 201-211.
    *Droes, R. M., Meiland, F. J., Schmitz, M. J., & van Tilburg, W. (2006). Effect of the Meeting Centres Support Program on informal carers of people with dementia: results from a multi-centre study. Aging and Mental Health, 10(2), 112-124.
    Dunkin, J. J., & Anderson-Hanley, C. (1998). Dementia caregiver burden: a review of the literature and guidelines for assessment and intervention. Neurology, 51(1 Suppl 1), S53-60; discussion S65-57.
    Dura, J. R., & Kiecolt-Glaser, J. K. (1990). Sample bias in caregiving research. Journal of gerontology, 45(5), 200-204.
    Edwards, M. (1990). Support groups for caregivers of Alzheimer's disease victims: the nurse's role. In C. Eliopoulos. (Eds.), Caring for the Elderly in Diverse Care Settings. Philadelphia: J. B. Lippincott Co.
    Etters, L., Goodall, D., & Harrison, B. E. (2008). Caregiver burden among dementia patient caregivers: A review of the literature. Journal of the American Academy of Nurse Practitioners, 20(8), 423-428.
    Ferri, C. P., Prince, M., Brayne, C., Brodaty, H., Fratiglioni, L., Ganguli, M., et al. (2005). Global prevalence of dementia: a Delphi consensus study. Lancet, 366(9503), 2112-2117.
    Folkman , S ., Lazarus , R . S ., Gruen, R. J., & DeLongis , A. (1986). Appraisal, coping, health status , and psychological symptoms. Journal of Personality and Social Psychology , 50 (3) , 571-579.
    Folstein, M. F., Folstein, S. E., & McHugh, P. R. (1975). Mini-mental state: A practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research, 12, 189-198.
    *Fung, W. Y., & Chien, W. T. (2002). The effectiveness of a mutual support group for family caregivers of a relative with dementia. Archives of Psychiatric Nursing, 16(3), 134-144.
    Gage, M. J., & Kinney, J. M. (1995). They aren’t for everyone: The impact of support group participation on caregiver’ well-being. Clinical Gerontologist, 16(2), 21-34.
    *Gallagher-Thompson, D., Arean, P., Rivera, P., & Thompson, L. W. (2001). A psychoeducational intervention to reduce distress in hispanic family caregivers: Results of a pilot study. Clinical gerontologist, 23(1), 17-32.
    Gallagher-Thompson, D., & Steffen, A. (1994). Comparative effects of
    cognitive-behavioral and brief psychodynamic psychotherapies for depressed family caregivers. Journal of Consulting and Clinical Psychology, 62, 543-549.
    Gallicchio, L., Siddiqi, N., Langenberg, P., & Baumgarten, M. (2002). Gender difference in burden and depression among informal caregivers of demented elders in the community. International Journal of Geriatric Psychiatry, 17(2), 154-163.
    *Gavrilova, S. I., Ferri, C. P., Mikhaylova, N., Sokolova, O., Banerjee, S., & Prince, M. (2008). Helping carers to care-The 10/66 dementia research group's randomized control trial of a caregiver intervention in Russia. International Journal of Geriatric Psychiatry, 24(4), 347-354.
    Gendron, C., Poitras, L., Dastoor, D. P., & Perodeau, G. (1996) Cognitive-behavior group intervention for spousal caregivers: Findings and clinical considerations. Clinical Gerontologist, 17(3), 19.
    George, L. K., & Gwyther, L. P. (1986). Caregiver well-being: a multidimensional examination of family caregivers of demented adults. Gerontologist, 26(3), 253-259.
    *Gitlin, L. N., Belle, S. H., Burgio, L. D., Czaja, S. J., Mahoney, D., Gallagher-Thompson, D., et al. (2003). Effect of multicomponent interventions on caregiver burden and depression: The REACH multisite initiative at 6-month follow-up. Psychology and Aging, 18(3), 361-374.
    Given, C. W., Collins, C. E., & Given, B. A. (1988). Sources of stress among families caring for relatives with Alzheimer’s disease. Nursing Clinics of North America, 23(1), 69-82.
    Glass, G. V. (1976). Primary, secondary, and meta-analysis of research. Educational Researcher, 5, 3-8.
    Glass, G. V., McGaw, B., & Smith, M. L. (1981). Meta-Analysis in Social Research. Beverly Hills, CA: Sage.
    Goldstein, V., Regnery, G., & Wellin, E. (1981). Caretaker role fatigue. Nursing Outlook, 29(1), 24-30.
    Gonyea, J. G. (1989). Alzheimer's disease support groups: an analysis of their structure, format and perceived benefits. Social Work in Health Care, 14(1), 61-72.
    Gonyea, J. G. (1990). Alzheimer’s disease support group participation and caregiver well-being. Clinical Gerontologist, 10(2), 17-34.
    Greene, V. L., & Monahan, D. J. (1989). The effect of a support and education program on stress and burden among family caregivers to frail elderly persons. The Gerontologist, 29(4), 472-477.
    Haley, W. E. (1997). The family caregiver's role in Alzheimer's disease. Neurology, 48(5 Suppl 6), 25-29.
    Haley, W. E., Brown, S. L., & Levine, E. G. (1987). Experimental evaluation of the effectiveness of group intervention for dementia caregivers. Gerontologist, 27(3), 376-382.
    Haley, W. E., West, C. A. C., Wadley, V. G., Ford, G. R., White, F. A., Barrett, J. J., et al. (1995). Psychological, social, and health impact of caregiving : a comparison of black and white dementia family caregivers and noncaregivers. Psychology and aging, 10(4), 540-552.
    Hardy, V. L., & Riffle, K. L. (1993). Support for caregivers of dependent elderly. A support group can help a dependent elderly person by helping a caregiver overcome feelings of social isolation. Geriatric Nursing, 14(3), 161-164.
    Harrison, L. L. (1996). Pulling it all together: the importance of integrative research reviews and meta-analyses in nursing. Journal of Advanced Nursing, 24(2), 224-225.
    *Hebert, R., Levesque, L., Vezina, J., Lavoie, J. P., Ducharme, F., Gendron, C., et al. (2003). Efficacy of a Psychoeducative Group Program for Caregivers of Demented Persons Living at Home: A Randomized Controlled Trial. The Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 58(1), 58-67.
    Hedges, L. V., & Olkin, I. (1985). Statistical methods for meta-analysis. New York: Academic Press.
    *Hepburn, K. W., Lewis, M., Narayan, S., Center, B., Tornatore, J., Bremer, K. L., et al. (2005). Partners in Caregiving: A Psychoeducation Program Affecting Dementia Family Caregivers' Distress and Caregiving Outlook. Clinical Gerontologist, 29(1), 53-70.
    *Hepburn, K. W., Lewis, M., Tornatore, J., Sherman, C.W., & Bremer, K. L. (2007). The Savvy Caregiver program: the demonstrated effectiveness of a transportable dementia caregiver psychoeducation program. Journal of gerontological nursing, 33(3), 30-36.
    *Hepburn, K. W., Tornatore, J., Center, B., & Ostwald, S. W. (2001). Dementia family caregiver training: affecting beliefs about caregiving and caregiver outcomes. Journal of the American Geriatrics Society, 49(4), 450-457.
    Higgins, J. P. T., Thompson, S. G., Deeks, J. J., & Altman, D. G. (2003). Measuring inconsistency in meta-analyses. British Medical Journal, 327, 557-560.
    Hozo, S. P., Djulbegovic, B., & Hozo, I. (2005).Estimating the mean and variance from the media, range, and the size of a sample. BMC Medical Research Methodology, 5(1), 13.
    Hughes, C. P., Berg, L., Danziger, W. L., Coben, L. A., & Martin, R. L. (1982). A new clinical scale for the staging of dementia. British Journal of Psychiatry, 140, 566-572.
    Hunter, J. E., & Schmidt, F. L. (1990). Methods of Meta-Analysis: Correcting error and bias in research findings. Newbury Park, CA: Sage.
    Jüni, P., Altman, D. G., & Egger, M. (2001). Systematic reviews in health care: Assessing the quality of controlled clinical trials. British Medical Journal, 323(7303), 42-46.
    Kaasalainen, S., Craig, D., & Wells, D. (2000). Impact of the Caring for Aging Relatives Group program: an evaluation. Public Health Nursing, 17(3), 169-177.
    Kahan, J., Kemp, B., Staples, F. R., & Brummel-Smith, K. (1985). Decreasing the burden in families caring for a relative with a dementing illness. A controlled study. The Journal of the American Geriatrics Society, 33(10), 664-670.
    Kim, N., Stanton, B., Li, X., Dickersin, K., & Galbraith, J. (1997). Effectiveness of the 40 adolescent AIDS-risk reduction interventions: A quantitative review. Journal of Adolescent Health, 20, 204–215.
    Kurtz, L. F. (1997). Self-help and support groups: A handbook for practitioners. Thousand Oaks, CA: Sage.
    Kutash, K., & Rivera, V. R. (1995). Effectiveness of Children's Mental Health Services: A Review of the Literature. Education and Treatment of Children, 18(4), 443-477.
    Lawton, M. P., Moss, M., Klebran, M. H., Glicksman, A., & Rovine, M. (1991). A two-factor model of caregiving appraisal and psychological well-being. Journal of Gerontology, 46(4), 181-189.
    Lewinsohn, P. M., Munoz, R. F., Youngren, M. A., & Zeiss, A. M. (1986). Control your depression. New York: Simon and Cchuster.
    Lipsey, M. W., & Wilson, D. B. (2001). Practical meta-analysis. Thousa- nd Oaks, CA: Sage.
    Liu, H. C., Lin, K. N., Tsou, H. K., Lee, K. M., Yan, S. H., & Wang, S. J. (1991). Impact of demented patients on their family members and care-givers in Taiwan. Neuroepidemiology, 10, 143-149.
    Lobo, A., Saz, P., Marcos, G., Dia, J. L., de la Camara, C., Ventura, T., et al. (1999). Revalidation and standardization of the cognition mini-exam (first Spanish version of the Mini-Mental Status Examination) in the general geriatric population. Medicina clínica, 112, 767–774.
    *Logsdon, R. G., McCurry, S. M., & Teri, L. (2006). Time-limited support groups for individuals with early stage dementia and their care partners: preliminary outcomes from a controlled clinical trial. Clinical Gerontology, 30(2), 5-19.
    Mannion, E., Meisel, M., Soloman, P., & Draine, J. (1996). A comparative analysis of families with mentally ill adult relatives: Support groups members versus non-members. Psychosocial Rehabilitational Journal, 20, 43-50.
    *Marriott, A., Donaldson, C., Tarrier, N., & Burns, A. (2000). Effectiveness of cognitive-behavioural family intervention in reducing the burden of care in carers of patients with Alzheimer's disease. The British Journal of Psychiatry, 176, 557-562.
    *Martin-Cook, K., Remakel-Davis, B., Svetlik, D., Hynan, L. S., & Weiner, M. F. (2003). Caregiver attribution and resentment in dementia care. American Journal of Alzheimer's Disease and Other Dementias, 18(6), 366-374.
    Mattis, S. (1988). Dementia rating scale: Professional manual. Odessa, FL: Psychological Assessment Resources.
    McCallion, P., & Toseland, R. W. (1995). Supportive Group Interventions with Caregivers of Frail Older Adults. Social Work with Group, 18(1), 11-25.
    Miller, B., & Cafasso, L. (1992). Gender differences in caregiving: Fact or artifact? The Gerontologist, 32, 498-507.
    Miller, J. E. (1998). Effective support groups. Indiana: Willowgreen
    Publishing.
    Miller, N., & Pollock, V. E. (1994). Meta-analytic synthesis for theory development. In H. Cooper & L. V. Hedges (Eds.), The handbook of research synthesis (pp. 457-483). New York: Russell Sage Foundation.
    Mittelman, M. S. (2000). Effect of Support and Counseling on Caregivers of Patients With Alzheimer's Disease. International Psychogeriatrics, 12, 341-346.
    Mittelman, M. S., Haley, W. E., Clay, O. J., & Roth, D. L. (2006). Improving caregiver well-being delays nursing home placement of patients with Alzheimer disease. Neurology, 67, 1592-1599.
    Monking, H. S. (1994). Self-help groups for families of schizophrenic patients: Formation, development and therapeutic impact. Social Psychiatry Psychiatr Epidemiology. 29, 149-154.
    Morgan, R., Luborsky, L., Crits-Christoph, P., Curtis, H., & Solomon, J. (1982). Predicting the outcomes of psychotherapy by the Penn Helping Alliance Rating Method. Archives of General Psychiatry, 39(4), 397-402.
    Morris, J. (1993). The CDR: current versions scoring rules. Neurology, 43, 2412-2413.
    Morrison, N. (2001). Group cognitive therapy: Treatment of choice or sub-optimal option? Behavioural and Cognitive Psychotherapy, 29, 311-332.
    Muskens, J. B. (1993). Het beloop van dementie; een exploratief longitudinaal onderzoek in de huisartsenpraktijk. [The course of dementia; an exploratory longitudinal study in general practice]. Academic thesis: Katholieke Universiteit Nijmegen.
    Nelis, S., Quinn, C., & Clare, L. (2007) Information and support interventions for informal caregivers of people with dementia. Cochrane Database of Systematic Reviews, 2, Art. No.: CD006440. DOI: 10.1002/14651858. CD0016440.
    Neundorfer, M. M., McClendon, M. J., Smyth, K. A., Stuckey, J. C., Strauss, M. E., & Patterson, M. B. (2001). A longitudinal study of the relationship between levels of depression among persons with Alzheimer’s disease and levels of depression among their family caregivers. Journal of Gerontology: Psychological Sciences, 56B, 301–313.
    *Onor, M. L., Trevisiol, M., Negro, C., Signorini, A., Saina, M., & Aguglia, E. (2007). Impact of a multimodal rehabilitative intervention on demented patients and their caregivers. American journal of Alzheimer's disease and other dementias, 22(4), 261-272.
    *Ostwald, S. K., Hepburn, K. W., Caron, W., Burns, T., & Mantell, R. (1999). Reducing caregiver burden: a randomized psychoeducational intervention for caregivers of persons with dementia. Gerontologist, 39(3), 299-309.
    Papastavrou, E., Kalokerinou, A., Papacostas, S. S., Tsangari, H., & Sourtzi, P. (2007). Caring for a relative with dementia: family caregiver burden. Journal of Advanced Nursing, 58(5), 446-457.
    Parker, D., Mills, S., & Abbey, J. (2008). Effectiveness of interventions that assist caregivers to support people with dementia living in the community: a systematic review International Journal of Evidence-based Healthcare, 6(2), 137-172.
    Peacock, S. C., & Forbes, D. A. (2003). Interventions for caregivers of persons with dementia: a systematic review. Canadian Journal of Nursing Research, 35(4), 88-107.
    Perline, L. I., Mullan, J. T., Semple, S. J., & Skaff, M. M. (1990). Caregiving and the stress process: An overview of concepts and their measures. The Gerontologist, 30(5), 583-594.
    *Perren, S., Schmid, R., & Wettstein, A. (2006). Caregivers' adaptation to change: the impact of increasing impairment of persons suffering from dementia on their caregivers' subjective well-being. Aging & mental health, 10(5), 539-548.
    Pinquart, M., & Sorensen, S. (2003). Associations of Stressors and Uplifts of Caregiving With Caregiver Burden and Depressive Mood: A Meta-Analysis. Journals of Gerontology Series B: Psychological Sciences and Social Sciences, 58(2), P112-128.
    Pinquart, M., & Sorensen, S. (2006a). Gender differences in caregiver experiences: an updated meta-analysis. Journal of Gerontology: Psychological Sciences, 61B, 33-45.
    Pinquart, M., & Sorensen, S. (2006b). Helping caregivers of persons with dementia : which interventions work and how large are their effects? International psychogeriatrics, 18(4), 577-595.
    Pusey, H., & Richards, D. (2001). A systematic review of the effectiveness of psychosocial interventions for carers of people with dementia. Aging & Mental Health, 5(2), 107-119.
    *Quayhagen, M. P., Quayhagen, M., Corbeil, R. R., Hendrix, R. C., Jackson, J. E., Snyder, L., et al. (2000). Coping with dementia: Evaluation of four nonpharmacologic interventions. International Psychogeriatrics, 12(2), 249-265.
    Reisberg, B. (1983). The Brief Cognitive Rating Scale and Global Deterioration Scale. In T. Crook, S. Ferris & C. Bartus (Eds.), Assessment in Geriatric psychopharmacology (pp. 19–35). New Canaan (Connecticut): Mark Powley.
    Reisberg, B., Ferris, S. H., De Leon, M. J., & Crook, T. (1982). The Global Deterioration Scale for assessment of primary degenerative dementia. The American Journal of Psychiatry, 139, 1136–1139.
    Reisberg, B., Ferris, S. H., De Leon, M. J., & Crook, T. (1988). The Global Deterioration Scale (GDS). Psychopharmacology Bulletin, 24, 661-669.
    Reisberg, B., Schneck, M., Ferris, S. H., Schwartz, G., & de Leon, M. J. (1983). The Brief Cognitive Rating Scale (BCRS): Findings in primary degenerative dementia (PDD). Psychopharmacology Bulletin, 19, 47-50.
    *Ripich, D. N., Ziol, E., & Lee, M. M. (1998). Longitudinal effects of communication training on caregivers of persons with alzheimer's disease. Clinical Gerontologis, 19(2), 37-55.
    Rosenthal, R. (1979). The File drawer problem and tolerance for null results. Psychological Bulletin, 86, 638-641.
    Rosenthal, R. (1991). Meta–analytic procedures for social research. Beverly Hills, CA: Sage.
    *Roth, D. R., Mittelman, M. S., Clay, O. J., Madan, A., & Haley, W. E. (2005). Changes in social support as mediators of the impact of a psychosocial intervention for spouse caregivers of persons with Alzheimer's disease. Psychology and Aging, 20(4), 634-644.
    Satterfield, J. (1998). Cognitive behavioral group therapy for depressed, low-income minority clients: Retention and treatment enhancement. Cognitive and Behavioral Practice, 5, 65-80.
    Schmall, V. L. (1984). It doesn't just happen: What makes a support group good? Generations, 9, 64-67.
    Schopler, J. H., & Galinsky, M. J. (1995). Expanding our view of support groups as open system. Social Work with Groups, 18(1), 3-10.
    Schulz, R., O'Brien, A., Czaja, S., Ory, M., Norris, R., Martire, L. M., et al. (2002). Dementia caregiver intervention research: in search of clinical significance. Gerontologist, 42(5), 589-602.
    Schweiger, J. L., & Huey, R. A. (1999). Alzheimer's disease: your role in the caregiving equation. Nursing, 29(6), 34-41.
    Selwood, A., Johnston, K., Katona, C., Lyketsos, C., & Livingston, G. (2007). Systematic review of the effect of psychological interventions on family caregivers of people with dementia. The Journal of Affective Disorders, 101(1-3), 75-89.
    *Senanarong, V., Jamjumras, P., Harmphadungkit, K., Klubwongs, M., Udomphanthurak, S., Poungvarin, N., et al. (2004). A counselling intervention for caregivers: effect on neuropsychiatric symptoms. International Journal of Geriatric Psychiatry, 19, 781-788.
    Sörensen, S., Pinquart, M., & Duberstein, P. (2002). How effective are interventions with caregivers? An updated meta-analysis. The Gerontologist, 42, 356-372.
    Stoller, E. P. (1990). Males as helpers: the role of sons, relatives, and friends. Gerontologists, 30(2), 228-235.
    Stommel, M., Given, C. W., & Given, B. G. (1990). Depression as an overriding variable explaining caregiver burden. Journal of Aging and Health, 2(1), 81-102.
    *Steffen, A. M. (2000). Anger management for dementia caregivers: A preliminary study using video and telephone interventions. Behavior Therapy, 31(2), 281-299.
    Stern, R., D'Ambrosio, L., Mohyde, M., Carruth, A., Tracton-Bishop, B., Hunter, J., et al. (2008). At the Crossroads: Development and Evaluation of a Dementia Caregiver Group Intervention to Assist in Driving Cessation. Gerontology & Geriatrics Education, 29(4), 363-382.
    Stock, W. M., Okum, M., Haring, M., Miller, W., Kinney, C., & Ceurvorst, R. (1982). Rigor in data analysis: A case study of reliability in meta-analysis. Educational Researcher, 11 (6), 10-20.
    Stone, R., Cafferata, G. L., & Sangl, J. (1987). Caregivers of the frail elderly: a national profile. Gerontologist, 27(5), 616-626.
    Tennstedt, S. L., Cafferata, G., & Sullivan, L. (1992). Depression among caregivers of impaired elderly. Journal of aging and health, 4(1), 58-76.
    Theis, S. L., & Johnson, J. H. (1995). Strategies for teaching patients: a meta-analysis. Clinical Nurse Specialists, 9(2), 100-105.
    Thoits, P. A. (1995). Stress, coping, and social suport processes: where are we? What next? Journal of Health and Social Behavior, 35, 53-79.
    Thompson, C., Spilsbury, K., Hall, J., Birks, Y., Barnes, C., & Adamson, J. (2007). Systematic review of information and support interventions for caregivers of people with dementia. BioMed Central Geriatrics, 7, 18-50.
    *Tompkins, S. A., & Bell, P. A. (2009). Examination of a psychoeducational intervention and a respite grant in relieving psychosocial stressors associated with being an Alzheimer’s caregiver. Journal of Gerontological Social Work, 52(2), 89-104.
    Toseland, R. W. (1990). Long-term effectiveness of peer-led and professiona- lly-led support groups for family caregivers. Social Service Review, 64(2), 308-327.
    Toseland, R. W., & Rossiter, C. M. (1989). Group interventions to support family caregivers: a review and analysis. Gerontologist, 29(4), 438-448.
    Toseland, R. W., Rossiter, C. M., & Labrecque, M. S. (1989). The effectiveness of peer-led and professionally led groups to support family caregivers. Gerontologist, 29(4), 465-471.
    *Ulstein, I. D., Sandvik, L., Wyller, T. B., & Engedal, K. (2007). A one-year randomized controlled psychosocial intervention study among family carers of dementia patients--effects on patients and carers. Dementia Geriatric Cognitive Disorders, 24(6), 469-475.
    Walsh, J. (1987). The family education and support group: A psycho- educational aftercare program. Psychosocial Rehabilitation Journal, 3, 51-61.
    Wilkins, S. S., Castle, S., Heck, E., Tanzy, K., & Fahey, J. (1999). Practical Geriatrics: Immune Function, Mood, and Perceived Burden Among Caregivers Participating in a Psychoeducational Intervention. Psychiatric Services, 50(6), 747-749.
    Wolf, F. M. (1986). Meta-analysis: Quantitative methods for research synthesis. Beverly Hills, CA: Sage.
    Yalom, I. D. (1995). The Theory and Practice of Group Psychotherapy, New York: Basic Books.
    Yalom, I. D. (2001).團體心理治療的理論與實務(方紫薇、馬宗潔譯).台北:桂冠。(原著出版於1995)
    *Yeung, C. M., & Chiu, L. (2004). Effectiveness of a psychogeriatric carer support group for alleviating carers' distress. Hong Kong Journal of Psychiatry, 14(4), 24-32.
    Zandi, T. (1990). Psychological difficulties of caring for dementia Patients: The role of support groups. In T. Zandi & R. J. Ham (Eds.), New directions in understanding dementia and Alzheimer’s disease. New York: Plenum Press.
    *Zanetti, O., Metitieri, T., Bianchetti, A., & Trabucchi, M. (1998). Effectiveness of an educational program for demented person's relatives. Archives of Gerontology and Geriatrics, 1998(6), 531-538.
    Zarit, S. H., & Leitsch, S. A. (2001). Developing and evaluating community based intervention programs for Alzheimer’s patients and their caregivers. Aging and Mental Healh, 5(Suppl. 1), S86-S100.
    顯示於類別:[學士後護理學系] 博碩士論文

    文件中的檔案:

    沒有與此文件相關的檔案.



    在TMUIR中所有的資料項目都受到原著作權保護.

    TAIR相關文章

    著作權聲明 Copyright Notice
    • 本平台之數位內容為臺北醫學大學所收錄之機構典藏,包含體系內各式學術著作及學術產出。秉持開放取用的精神,提供使用者進行資料檢索、下載與取用,惟仍請適度、合理地於合法範圍內使用本平台之內容,以尊重著作權人之權益。商業上之利用,請先取得著作權人之授權。

      The digital content on this platform is part of the Taipei Medical University Institutional Repository, featuring various academic works and outputs from the institution. It offers free access to academic research and public education for non-commercial use. Please use the content appropriately and within legal boundaries to respect copyright owners' rights. For commercial use, please obtain prior authorization from the copyright owner.

    • 瀏覽或使用本平台,視同使用者已完全接受並瞭解聲明中所有規範、中華民國相關法規、一切國際網路規定及使用慣例,並不得為任何不法目的使用TMUIR。

      By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in the statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions. Furthermore, users must not use TMUIR for any illegal purposes.

    • 本平台盡力防止侵害著作權人之權益。若發現本平台之數位內容有侵害著作權人權益情事者,煩請權利人通知本平台維護人員([email protected]),將立即採取移除該數位著作等補救措施。

      TMUIR is made to protect the interests of copyright owners. If you believe that any material on the website infringes copyright, please contact our staff([email protected]). We will remove the work from the repository.

    Back to Top
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋