字體大小: 字級放大   字級縮小   預設字形  

詳目顯示

以作者查詢圖書館館藏以作者&題名查詢臺灣博碩士以作者查詢全國書目
研究生中文姓名:張洛嘉
中文論文名稱:慢性中風失語症患者之健康相關生活品質及其相關因素探討
指導教授姓名:盧璐
學位類別:碩士
校院名稱:臺北市立教育大學
系所名稱:溝通障礙碩士學位學程
論文出版年:98
畢業學年度:97
語文別:中文
論文頁數:166
中文關鍵詞:失語症生活品質語言損傷程度功能性溝通能力情緒狀態
英文關鍵字:aphasiaHRQOLseverity of language impairmentfunctional communication abilityemotional status
相關次數:
  • 推薦推薦:0
  • 點閱點閱:158
  • 評分評分:系統版面圖檔系統版面圖檔系統版面圖檔系統版面圖檔系統版面圖檔
  • 下載下載:0
  • 收藏收藏:0
腦中風常造成失語症,在成人溝通障礙中可說是影響層面最廣的一種。近年來學界越來越重視由患者自身的角度來瞭解疾病的影響以及醫療介入的成效或必要性,健康相關生活品質的評估就是其中的代表。過去針對失語症患者健康生活品質之相關研究仍然不多,且往往並未控制肢體行動障礙這個也會對健康生活品質造成重大影響的變項。

故本研究擬控制肢體動作障礙方面的差異之後,比較中風後有失語症與無失語症兩組患者的健康相關生活品質,以瞭解失語症的存在對生活品質所造成的影響。同時進一步探討可能影響失語症患者健康相關生活品質的因素,包括其『語言損傷嚴重度』、『功能性溝通能力』、個人情緒狀態及其它人口統計學變項(年紀、性別、教育程度、婚姻狀況、職業、主要照顧者)、中風相關變項(中風後時間、中風類型、罹患疾病數)與生活品質的關連性。

本研究對象為26名失語症患者,並以23名中風無失語症患者為對照組,兩組個案在基本日常生活功能、人口統計學變項及中風相關變項方面均無顯著差異。所有個案均以訪談方式完成『巴氏量表』及『中風失語症生活品質量表中文版(SAQOL-C)』的評估,失語症組個案另外亦接受『中風負擔量表(BOSS)』、『華譜失語症測驗(WAB)』、『溝通效益測驗(CETI)』、『貝克憂鬱量表(BDI-II)』的評估。結果顯示,慢性中風失語症患者在SAQOL-C的溝通相關及整體健康相關生活品質方面都比沒有失語症的對照組差,但在生理、心理社會及能量方面,兩組之間並沒有顯著差異。

另外,失語症患者的語言損傷程度越嚴重、功能性溝通能力越差,其整體健康生活品質越差,在溝通方面感受到的困擾越多、自我感知在溝通及社會關係上呈現出較多的困難,但與其心理苦惱程度並無顯著相關。在個人因素方面,憂鬱程度越高者其在能量方面感受到的困擾越多;罹患疾病數越多者,在SAQOL-C能量及整體健康相關生活品質上也感覺到比較多的困擾,且認知相關心理苦惱較多。

整體而言,失語症確實會對慢性中風患者的健康生活品質造成不利的影響。
To assess the impact of diseases and the effect or necessity of medical interventions through the patients’ point of view has drawn more and more attention in the medical field. This has been reflected by the growing number of studies on the assessment of health related quality of life (HRQOL) after various diseases. Aphasia is common after stroke and is probably the one with most pervasive influence among adult communication disorders. However, there had been limited studies of the HRQOL on aphasic patients. Besides, motor disability, which is a common co-morbidity of stroke related aphasia and might also affect HRQOL greatly, was rarely controlled in previous studies.
The purpose of this study is to compare the HRQOL among chronic stroke patients with and without aphasia, after controlling the factor of motor disability using Bathel Index and Brunnstrom staging. Furthermore, the correlation between aphasic patients HRQOL and possible variables were investigated, including the severity of aphasia, the functional communication ability, personal factors such as emotional status, demographic variables (age, gender, education level, marital status, employment, and main care) and stroke-related variables (time post-onset, type of stroke, disease number).
26 stroke patients with aphasia, and 23 stroke patients without aphasia were recruited in this study. They were matched in daily activities functions, demographic variables, and the stroke-related health variables. All subjects were interviewed with SAQOL-C for assessment of their HRQOL. The aphasic patients were further assessed by the Bound of Stroke Scale (BOSS), the Western Aphasia Battery (WAB), the Communicative Effectiveness Index (CETI), and the Beck Depression Inventory- Second Edition (BDI-II) to assess their HRQOL, severity of language impairment, functional communication ability, and degree of depression respectively.
It was shown that, comparing to stroke patients without aphasia, the aphasic patients reported significantly lower overall HRQOL on the SAQOL-C total score, and the communication subscale, but there is no significant difference on the physical, psychosocial, and energy subscales between the two groups. Furthermore, patients with more severe language impairment or higher communication disability reported significantly poorer total HRQOL on the SAQOL-C, and perceived greater difficulties in communication and social relationships on the BOSS. However, it was not correlated with the subjects’ psychological distress. People with higher depression perceived more trouble in the energy subscale of SAQOL-C. People with more co-morbid diseases also perceived more trouble in the energy subscale of SAQOL-C and had poorer total HRQOL and more cognition associated psychological distress.
In conclusion, the presence of aphasia could have adverse effect on chronic stroke patients’ HRQOL.
頁數
謝誌………………………………………………………………… I
摘要………………………………………………………………… II
目錄…………………………………………………………………… VII
附錄目錄………………………………………………………………… VIII
表目次………………………………………………………………… IX圖目次………………………………………………………………… X
第一章 緒論
第一節 研究背景與動機………………………………………… 1
第二節 研究目的………………………………………………… 8
第三節 研究問題與研究假設…………………………………… 9
第四節 名詞解釋………………………………………………… 10
第二章 文獻探討
第一節 健康相關生活品質的概念……………………………… 13
第二節 失能與生活品質之間的關係…………………………… 28
第三節 失語症患者的健康相關生活品質……………………… 34
第三章 研究方法
第一節 研究架構………………………………………………… 47
第二節 研究設計………………………………………………… 49
第三節 研究工具………………………………………………… 52
第四節 研究對象………………………………………………… 63
第五節 資料收集與分析………………………………………… 72
第四章 研究結果
第一節 有失語症與無失語症之慢性中風患者於SAQOL-C
之表現差異………………………………………………… 74
第二節 失語症患者中風負擔量表、語言損傷程度、
功能性溝通能力及憂鬱狀況之表現……………………… 78
第三節 失語症患者語言損傷程度與健康相關生活品質之關係… 86
第四節 失語症患者功能性溝通能力與健康相關生活品質之關係… 88
第五節 失語症患者憂鬱情緒與健康相關生活品質之關係……… 90
第六節 失語症患者人口統計學變項及中風相關變項
與健康相關生活品質之關係……………………………… 92
第五章 討論
第一節 失語症對慢性中風患者健康相關生活品質的影響………. 94
第二節 影響失語症患者健康相關生活品質之相關因素…………. 99
第三節 SAQOL-C與BOSS內容及施測結果比較………………… 110
第六章 結論與建議
第一節 結論………………………………………………………….... 113
第二節 研究限制…………………………………………………….... 115
第三節 建議………………………………………………………….... 118
參考文獻
中文部分……………………………. ................ 122
西文部分.................................................124
附錄
附錄一 ICF架構各範疇間彼此交互關係………………………......... 137
附錄二Communication-related QOL (CRQOL)模式…………………… 138
附錄三 受試者資料調查表…………………………………………… 139
附錄四 SAQOL-39中文版…………………………………………… 140
附錄五 中風負擔量表………………………………………………… 142
附錄六 溝通效益測驗………………………………………………… 147
附錄七 巴氏量表……………………………………………………… 150
附錄八 受試者同意書………………………………………………… 151
附錄九 台大醫院受試者同意書……………………………………… 152


表目次
頁數
表 2-1 常用之健康相關生活品質量表特色………………………… 24
表 3-3 研究工具內部一致性(Cronbach’s α值) ……………………… 62
表 3-4-1 失語症與無失語症組之人口基本特性…………………… 67
表 3-4-2 失語症與無失語症組中風相關變項…………………… 68
表 3-4-3 失語症組與無失語症組人口基本特性同質性檢定…………… 70
表 3-4-4 失語症組與無失語症組中風相關變項同質性檢定…………… 71
表 4-1-1 研究對象於SAQOL-C之平均分數、標準差、t考驗結果….. 76
表 4-1-2 研究對象於SAQOL-C之題目細項結果……………………… 77
表 4-2-1 失語症組受試者於BOSS各分量表之表現…………………… 80
表 4-2-2 失語症組受試者於BOSS之題目細項結果…………………… 80
表 4-2-3 失語症組受試者於BOSS各分量表間相關…………………… 82
表 4-2-4 華譜失語症測驗結果…………………………………………… 82
表 4-2-5 失語症組受試者語言損傷程度………………………………… 83
表 4-2-6 失語症組受試者於溝通效益測驗之表現……………………… 83
表 4-2-7 失語症組受試者於功能性溝通評量之題目細項結果………… 83
表 4-2-8 失語症組受試者於貝克憂鬱量表第二版之表現……………… 85
表 4-2-9 失語症組受試者於憂鬱評量之題目細項結果………………… 85
表 4-3-1 失語症組受試者之語言損傷程度與 SAQOL-C之相關……… 87
表 4-3-2 失語症組受試者之語言損傷程度與BOSS之相關…………… 87
表 4-4-1 失語症組受試者功能性溝通能力與SAQOL-C之相關……… 89
表 4-4-2 失語症組受試者功能性溝通能力與BOSS之相關…………… 89
表 4-5-1 失語症組受試者之憂鬱狀態與SAQOL-C之相關…………… 91
表 4-5-2 失語症組受試者之憂鬱狀態與BOSS之相關………………… 91




圖目次
頁數
圖2-1 QOL、HRQOL、HS三個概念圖…………………… 16
圖2-2 失能模式與健康相關生活品質間的關連性……… 32
圖2-3 A-FROM架構中範疇及類別模式範例…………… 39
圖3-1 研究架構圖………………………………………… 48
圖3-2 研究設計圖………………………………………… 50
中文部分

台灣長期照護專業協會(2005)。評估量表下載。(下載日期 12, 30, 2008, http: www.ltcpa.org.tw/public/download.html)。

李登裕(2004)。頭部外傷患者健康相關生活品質之探討。台北醫學大學傷害防治學研究所碩士論文。

吳侑璇(2005)。失語症病患功能性溝通能力之研究。國立台北護理學院聽語障礙科學研究所碩士班論文。

邱弘毅(民97)。腦中風之現況與流行病學特徵。台灣腦中風學會會訊。15, 3。

柯秀芬(2009)。生活品質量表-中文版的信效度研究。台北市立教育大學溝通障礙教育碩士學位學程碩士論文。

姚開屏(2000)。簡介與評論常用的一般性健康相關生活品質量表兼談對未來研究的建議。中國測驗學會測驗年刊, 47(2), 111-138。

姚開屏(2002)。健康相關生活品質概念與測量原理之簡介。台灣醫學會, 6(2), 183-192。

姚開屏 (2002)。台灣版世界衛生組織生活品質問卷之發展與應用。台灣醫學會, 6(3), 193-200。

陳心怡譯(2000)。貝克憂鬱量表第二版(Beck Depression Inventory-II, BDI-II)中文版指導手冊。台北:中國行為科學社。

張彧、王顏和、姚開屏、王榮德(2002)。脊髓損傷生活品質問卷之發展。台灣醫學會, 6(2), 209-214。

張瑞昆、陳正岳、梁秋萍(1992)。腦中風病人情緒障礙之探討。職能治療學會雜誌, 10, 43-54。

梁文敏、陳建仲、張郁瑩、王昶弼、夏德樁、杭良文、顏至慶、李長興、陳怡文、施富金 (2002)。焦點團體法在生活品質測量之應用—以慢性阻塞性肺疾病為例。台灣醫學會, 6(2), 201-208。

曾旭民、盧瑞芬、蔡益堅 (2003)。國人生活品質評量(II):SF-36台灣版的常模與效度檢測。台灣衛誌, 22, 512-518。

楊美倫(2003)。中風失能患者自我概念、社會支持與憂鬱相關因素之探討。中山醫學大學醫學研究所碩士論文。

廖惠鶯(民93)。中老年失語症患者功能性溝通需求與表現。國立高雄師範大學溝通障礙教育研究所碩士論文。

盧瑞芬、曾旭民、蔡益堅 (2002)。國人生活品質評量(I):SF-36台灣版的發展及心理計量特質分析。台灣衛誌, 22(6), 501-511。

戴玉慈、羅美芳(民85)。身體功能評估的概念與量表。護理雜誌, 43(2), 63-68。

鍾玉梅、李淑娥、張妙鄉 (2002):簡明失語症測驗指導手冊。台北:心理出版社。

西文部分

American Speech-Language-Hearing Association (ASHA) (1992). Meeting the communication needs of persons with severe disabilities. Asha, 34, 1-8.

American Speech-Language-Hearing Association (ASHA) (2001). Scope of practice for speech-language pathology. Rockville, MD: ASHA.

Addington-Hall, J., & Kalra, L. (2001). Mrasuring Quality of Life: Who should measure quality of life? BMJ, 322, 1417-1420.

Aben, I., Verhey, F., Lousberg, R., Lodder J., & Honig, A. (2002). Validity of the Beck Depression Inventory, Hospital Anxiety and Depression Scale, SCL-90, and Hamilton Depression Rating Scale as Screening Instruments for Depression in Stroke Patients. Psychosomatics, 43, 386-393.

Brief, A. P., Butcher, A. H., George, J. M., Link, K. E., (1993). Integrating Bottom-Up and Top-Down theories of subjective well-being: The case of health. Journal of Personality and Social Psychology, 64, 646-653.

Bickenbach, J. E., Chatterji, S., Badley, E. M., & Ustun, T. B., (1999). Models of disablement, universalism and the international classification of impairments, disabilities and handicaps. Social Science & Medicine, 48, 1173-1187.

Brookshire, R. H. (2003). Neuroanatomic Explanations of Aphasia and Related Disorders. In Brookshire, R. H. ( 6 nd ed), Introduction to Neurogenic Communication Disorders. Missouri: Mosby.

Brookshire, R. H. (2003). Neuroanatomy and Neuropathology. In Brookshire, R. H. ( 6 nd ed), Introduction to Neurogenic Communication Disorders. Missouri: Mosby.

Brumfitt, S., (2006). Psychosocial aspects of aphasia: Speech and language therapists’ views on professional practice. Disability and Rehabilitation, 28, 523 – 534.

Cruice, M., Worrall, L., Hickson, L. Hirsch, F., & Holland, A., (2000). Quality of life for people with aphasia: performance on and usability of quality of life assessments. Asia Pacific Journal of Speech, Language and Hearing, 5, 85-91.

Chapey, R., & Hallowell, B., (2001). Introduction to Language Intervention Strategies in Adult Aphasia. In R. Chapey, (4 nd ed.), Language Intervention Strategies in Aphasia and Related Neurogenic Communication Disorders. New York: Lippincott Williams & Wilkins.

Cherney, L. R., & Robey, R. R., (2001). Aphasia treatment: Recovery, Prognosis, and Clinical Effectiveness. In R. Chapey, (4 nd ed.), Language Intervention Strategies in Aphasia and Related Neurogenic Communication Disorders. New York: Lippincott Williams & Wilkins.

Code, C. (2003). The quantity of life for people with chronic aphasia. Neuropsychological Rehabilitation, 13, 379-390.

Cruice, M., Worrall, L., Hickson, L., & Murison, R., (2003). Finding a focus for quality of life with aphasia: Social and emotional health, and psychological well-being. Aphasiology, 17, 333-353.

Cruice, M., Worrall, L., Hickson, L., & Murison, R., (2005). Measuring quality of life: Comparing family members’ and friends’ ratings with those of their aphasic partners. Aphasiology, 19, 119-129.

CureResearch.com. (2007, September). Prevalence and Incidence of Aphasia. (Accessed November 20, 2008, http://www.cureresearch.com/a/aphasia/prevalence.htm).

Cruice, M. (2008). The contribution and impact of the International classification of functioning, disability and health on quality of life in communication disorders. International Journal of Speech-Language Pathology, 10, 38-49.

De Haan, R., Horn, J., Limburg, M., Van Der Meulen, J., & Bossuyt, P., (1993). Stroke Scales and Functional Health Outcomes. Stroke, 24, 1178-1181.

deHaan, M. S. R., Aaronson, N., Limburg, M., Langton Hewer, R. & Van Crevel, H., (1993).Measuring quality of life in stroke. Stroke, 24, 320-327.

Day, H., & Jankey, S. G., (1996). Lessons from the literature: Toward a holistic model of quality of life. In R. Renwick, I. Brown, & M. Nagler (Eds.), Quality of life in Health Promotion and Rehabilitation (p. 39-62). Thousand Oaks, CA: Sage.

Duncan, P. W., Jorgensen, H. S, & Wade, D. T., (2000). Outcome Measures in Acute Stroke Trials A Systematic Review and Some Recommendations to Improve Practice. Stroke, 31, 1429-38.

Draper, P., & Thompson, D. R., (2001). The Quality of Life –A concept for research and practice. Journal of Research in Nursing, 6, 648-656.

Doyle, P. J. (2002). Measuring Health Outcomes in Stroke Survivors. Arch Phys Med Rehabil, 83, S39-43.

Doyle, P. J., McNeil, M. R., & Hula, W. D., (2003). The Burden of Stroke Scale (BOSS): Validating patient-reported communication difficulty and associated psychological distress in stroke survivors. Aphasiology, 17, 291-304.

Doyle, P. J., McNeil, M. R., Mikolic, J. M., Prieto, L., Hula, W. D., Lustig, A. P., Ross, K., Wambaugh, J. L., Gonzalez-Rothi, L. J., & Elman, R. J. (2004). The Burden of Stroke Scale (BOSS) provides valid and reliable score estimates of functioning and well-being in stroke survivors with and without communication disorders. Journal of Clinical Epidemiology, 57, 997-1007.

Doyle, P. J., Matthews, C., Mikolic, J. M., Hula, W., & McNeil, M. R., (2006). Do measures of language impairment predict patient-reported communication difficulty and distress as measured by the Burden of Stroke Scale (BOSS)? Aphasiology, 20, 349-361.

Doyle, P. J., McNeil, M. R., Bost, J. E., Ross, K. B., Wambaugh, J. L., Hula, W. D., & Mikolic, J. M., (2007). The Burden of Stroke Scale (BOSS) provides valid, reliable, and responsive score estimates of functioning and well-being during the first year of recovery from stroke. Quality of Life Research, 16, 1389-1398.

Engell, B., Hutter, B. O., Willmes, K., & Huber, W., (2003). Quality of life in aphasia: Validation of a pictotial self-rating procedure. Aphasiology, 17, 383-396.

Fuhrer, M. (1994). Subjective well-being: Implications for medical rehabilitation outcomes and models of disablement. American Journal of Physical Medicine and Rehabilitation, 73, 358-364.

Frattali, C. M., Thompson, C. M., Holland, A. L., Wohl, C. B. & Ferketic, M. M., (1995). Function assessment of communication skills for adults. ASHA.
Goodglass, H., & Kaplan, E., (1984). Assessment of aphasia and related disorders, 2nd. Philadelphia: Lea & Febiger.

Guyatt, G. H., Feeny, D. H., & Patrick, D. L. (1993). Measuring Health-related Quality of Life. Annals of Internal Medicine, 118, 622-629.

Geyh, S., Cieza, A., Kollerits, B., Grimby, G., & Stucki, G., (2007). Content comparison of health-related quality of life measures used in stroke based on the international classification of functioning, disability and health (ICF): a systematic review. Quality of Life Research, 16, 833-851.

Haan, R. D., Horn, J., Limburg, M., Meulen, J., Bossuyt, P., (1993). A Comparison of Five Stroke Scales With Measures of Disability, Handicap, and Quality of Life. Stroke, 24, 1178-1181.

Hemsley, G., & Code, C., (1996). Interactions between recovery in aphasia, emotional and psychosocial factors in subjects with aphasia, their significant others and speech pathologists. Disability and Rehabilitation, 18, 567-584.

Haas, B. K. (1999). A Multidisciplinary Concept Analysis of Quality of Life. Wester Journal of Nursing Research, 21, 728-742.

Hackett, M. L., Duncan, J. R., Anderson, C. S., Broad, J. B., & Bonita, R., (2000). Health-Related Quality of Life Among Long-Term Survivors of Stroke. Stroke, 31, 440-447.

Hilari, K., & Byng, S., (2001). Measuring Quality of life in people with aphasia:The Stroke Specific Quality of Life Scale. International Journal of Language & Communication Disorders, 36 (Suppl.), 86-91.

Hilari, K., Byng, S., Lamping, D., & Smith, S. C., (2002). The Stroke and Aphasia Quality of Life Scale- 39 Item Version (SAQOL-39). Quality of Life Research, 11, 651.

Hilari, K., Byng, S., Lamping, D. L., & Smith, S. C., (2003). Stroke and Aphasia Quality of Life Scale-39 (SAQOL-39):Evaluation of Acceptability, Reliability, and Validity. Stroke, 34, 1944-1950.

Hilari, K., Wiggins, R. D., Roy, P., Byng, S., & Smith, S. C., (2003). Predictors of health-related quality of life (HROL) in people with chronic aphasia. Aphasiology, 17, 365-381.

Haynes, W. O., & Pindzola, R. H., (2004). Diagnosis and evaluation in Speech Pathology, 6 nd ed. Boston: Pearson Allyn and Bacon.

Hilari, K., & Northcott, S., (2006). Social support in people with chronic aphasia. Aphasiology, 20, 17-36.

Hilari, K., & Byng, S., (2008). Health-related quality of life in people with severe aphasia. International Journal of Language & Communication Disorders, 1-13.

Howe, T. J. (2008). The ICF Contextual factors related to speech-language
pathology. International Journal of Speech-Language Pathology, 10, 27-37.

Jonkman, E. J., de Weerd, A. W., & Vrijens, NLH., (1998). Quality of life after a first ischemic stroke. Acta Neurol Scand, 98, 169-175.

Jonsson, A., Lindgren, I., Hallstrom, B., Norrving, B., & Lindgren, A., (2005). Determinants of Quality of Life in Stroke Survivors and Their Informal Caregivers. Stroke, 36, 803-808.

Kertesz, A. (1982). Western Aphasia Battery. New York: Grune and Stratton.

King, R. B. (1996). Quality of Life after Stroke. Stroke, 27, 1467-1472.

Kotila, M., Numminen, H., Waltimo, O., & Kaste, M., (1998). Depression After Stroke : Results of the FINNSTROKE Study. Stroke, 29, 368-372.

Kertesz, A. (2007). Western Aphasia Battery, revised. San Antonio: PsychCorp.

Kartsona, A., & Hilari, K., (2006). Quality of life on aphasia: Greek adaptation of the stroke and aphasia quality of life scale-39 item (SAQOL-39). Europa Medico Physica, 42, 1-8.

Kagan, A., Simmons-Mackie, N., Rowland, A., Huijbregts, M., Shumway, E., McEwen, S., Threats, T., & Sharp, S., (2008). Counting what counts: A Framework for capturing real-life outcomes of aphasia intervention. Aphasiology, 22, 258-280.

Lomas, J., Pickard, L., Bester, S., Elbard, H., Finlayson, A. & Zogh-aib, C., (1989). The Communication Effectiveness Index: Development and psychometric evaluation of a functional communication measure for adult aphasia. Journal of Speech and Hearing Disorders, 54, 113-124.

Lyon, J. G., Cariski, D., Keisler, L., Rosenbek, J., Levine, R., Kumpula, J., Ryff, C., Coyne, S., & Blanc, M., (1997). Communication partners: Enhancing participation in life and communication for adults with aphasia in natural settings. Aphasiology, 11, 693-708.

Lincoln, N. B., C. R. Nicholl, T. Flannaghan, M. Leonard, & E. Van der Gucht, (2003). The validity of questionnaire measures for assessing depression after stroke. Clinical Rehabilitation, 17, 840-846.

Murray, L. L. & Chapey, R. (2001). Assessment of language disorders in Adults. In R. Chapey (4 nd ed.), Language Intervention strategies in aphasia and related neurogenic communication disorders. New York: Lippincott Williams & Wilkins.

National Aphasia Association. (2008, November). Aphasia Frequently Asked Questions. (Accessed November 19, 2008, http://www.aphasia.org/Aphasia/Facts/aphasia_faq.html).

National Institute on Deafness and Other Communication Disorders. (2008, November). Facts Sheet: Aphasia (NIH Pub. NO. 97-4257). Bethesda, MD: Author.

Pohjasvaara, T., Leppavuori, A., Siira, I., Vataja, R., Kaste, M., & Erkinjuntti, T., (1998). Frequency and Clinical Determinants of Poststroke Depression. Stroke, 29, 2311-2317.

Post, M. W., de Witte, L. P., & Schrijwars, A. J. P., (1999). Quality of life and the ICIDH: toward an integrated conceptual model for rehabilitation outcomes research. Clinical Rehabilitation, 13, 5-15.

Pfeiffer, D., (2000). The Devils are in the Details: the ICIDH2 and the disability. Disability & Society, 15, 1079-1082.

Pelletier, G., Verhoef, M. J., Khatri, N., & Hagen, N., (2002). Quality of Life in Brain Tumor Patients: The Relative Contributions of Depression, Fatigue, Emotional Distress, and Existential Issues. Journal of Neuro-Oncology, 57, 41-49.

Posteraro, L., Formis, A., Grassi, E., Bighi, M., Nati, P., Bocchini, C., Todeschini, E., Bidini, C., Corsini, D., Agosti, M., & Franceschini, M., (2006). Quality of life and aphasia. Multicentric standardization of a questionnaire. Europa Medicophysica, 42, 227-230.

Ross, K. B. & Wertz, R. T., (2002). Relationships between language-based disability and quality of life in chronically aphasic adults. Aphasiology, 16, 791-800.

Ross, K. B. & Wertz, R. T., (2003). Quality of life with and without aphasia. Aphasiology, 17, 355-364.

Spitzer, W. O., (1987). Quality of life and functional status as target variables for research. Journal of Chronic Diseases, 40, 465-471.

Straten, A. V., Haan, R. J., Limburg, M., Schuling, J., Bossuyt, P. M. & van den Bos, G. A. M., (1997). A Stroke-Adapted 30-Item Version of the Sickness Impact Profile to Assess Quality of Life (SA-SIP30). Stroke, 28, 2155-61.

Saron, M. T., (1997). Quality of life in aphasia in the first post-stroke year. Aphasiology, 11, 665-679.

Sneeuw, K. C., Sprangers, M. A., & Aaronson, N. K., (2002). The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease. Journal of Clinical Epidemiology, 55, 1130-1143.

Simmons-Mackie, N., & Kagan, A., (2007). Application of the ICF in Aphasia. Seminars in Speech and Language, 28, 244-253.
Testa, M. A., & Simonson, D. C., (1996). ASSESSMENT OF QUALITY-OF–LIFE OUTCOMES. The New England Journal of Medicine, 334, 835-840.

The WHOQOL Group (1994). The development of the World Health Organization Quality of Life Assessment Instrument (the WHOQOL): In J. Orley, & W. Kuyken (Eds.), Quality of Life Assessment: International Perspetives. Heidelberg: Springer-Verlag.

The WHOQOL Group (1995). The World Health Organization quality of life assessment (WHOQOL): position paper from the world health orhanization. Social Science Medicine, 41, 1403-1409.

The WHOQOL Group (1996). What quality of life? World Health Forum, 17, 354-356.

Threats, T. T., (2006). Toward an international framework for communica-
tion disorders: Use of the ICF. Journal of Communication Disorders, 39, 251-265.

Ueda, S., & Okawa, Y., (2003). The subjective dimension of functioning and disability: what is it and what is it for. Disability and Rehabilitation, 25, 596-601.

Ware, J. J., & Sherbourne, C. D., (1992). The MOS 36-item short-form survey (SF-36): I Conceptual framework and item selection. Medical Care, 30, 473-483.
Williams, L. S., Weinberger, M., Harris, L. E., & Biller, J., (1999). Measuring quality of life in a way that is meaningful to stroke patients. Neurology, 53, 1839-1849.

Williams, L. S., Weinberger, M., Harris, L. E., Clark, D. O., & Biller, J., (1999). Development of a Stroke-Specific Quality of Life Scale. Stroke, 30, 1362-1369.

World Health Organization (2001). International Classification of Functioning, Disability, and Health. Geneva, Switzerland: World Health Organization.

Worrall, L., McCooey, R., Davidson, B., Larkins, B., & Hickson, L., (2002). The validity of functional assessments of communication and the Activity/Participation components of the ICIDH-2: do they reflect what really happens in real-life? Journal of Communication Disorders, 35, 107-137.

Worrall, L. E., & Holland, A. L., (2003). Quality of life in aphasia. Aphasiology, 17, 329-332.

World Health Organization (2007). International Classification of Functioning, Disability, and Health Children & Youth Version. Switzerland: World Health Organization.
(此全文未開放授權)
封面(書名頁)
摘要
謝誌
目錄
第一章
第二章
第三章
第四章
第五章
第六章
參考文獻
附錄
校內電子全文開放日期:不公開
校外電子全文開放日期:不公開
 
 
 
 
第一頁 上一頁 下一頁 最後一頁 top
* *