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| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 曾美惠(Mei-Hui Tseng) | |
| dc.contributor.author | Shao-Ju Chang | en |
| dc.contributor.author | 張卲如 | zh_TW |
| dc.date.accessioned | 2021-06-15T12:31:56Z | - |
| dc.date.available | 2021-08-26 | |
| dc.date.copyright | 2016-08-26 | |
| dc.date.issued | 2016 | |
| dc.date.submitted | 2016-08-03 | |
| dc.identifier.citation | Adolfsson, M. (2011). Applying the ICF-CY to identify everyday life situations of
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Quality of life instruments for children and adolescents with neurodisabilities: how to choose the appropriate instrument. Developmental Medicine & Child Neurology, 51(8), 660-669. doi: 10.1111/j.1469-8749.2009.03324.x Waters, E., Maher, C., Salmon, L., Reddihough, D., & Boyd, R. (2005). Development of a condition-specific measure of quality of life for children with cerebral palsy empirical thematic data reported by parents and children. Child Care Health and Development, 31(2), 127-135. World Health Organization: WHOQOL: Measuring quality of life. Retrieved from :[http:// www.who.int/mental_health/media/68.pdf] WHOQOL Group (1998). The World Health Organization Quality of Life Assessment (WHOQOL). Development and psychometric properties. Social Science & Medicine, 46:1569-1585. World Health Organization (2007). International Classification of Functioning, Disability and Health Children & Youth Version (ICF-CY). Retrieved from : http://apps.who.int/iris/bitstream/10665/43737/1/9789241547321_eng.pdf White-Koning, M., Arnaud, C., Bourdet-Loubere, S., Bazex, H., Colver, A., & Grandjean, H. (2005). Subjective quality of life in children with intellectual impairment–how can it be assessed. Developmental Medicine & Child Neurology, 47, 281-285. White-Koning, M., Arnaud, C., Dickinson, H. O., Thyen, U., Beckung, E., Fauconnier, J., . . . Colver, A. (2007). Determinants of child-parent agreement in quality-of-life reports: A European study of children with cerebral palsy. Pediatrics, 120(4), 804-814. doi: 10.1542/peds.2006-3272 Williams, B., Brown, T., & Onsman, A. (2010). Exploratory factor analysis: A five-step guide for novices. Australian Journal of Paramedicine, 8(3). Yang, X., Xiao, N., & Yan, J. (2011). The PedsQL in pediatric cerebral palsy: reliability and validity of the Chinese version pediatric quality of life inventory 4.0 generic core scales and 3.0 cerebral palsy module. Quality of Life Research, 20(2), 243-252. doi: 10.1007/s11136-010-9751-0 Yao, G., Chung, C. Y., Yu, C. F., & Wang, J. D. (2002). Development and verfication of validity and reliabilty of the WHOQOL-BREF Taiwan version. Journal of the Formosan Medical Association, 101, 342-351. Yong, A.G. & Pearce, S. (2013). A beginner’s guide to factor analysis: Focusing on exploratory factor analysis. Tutorials in Quantitative Methods for Psychology, 9 (2), 79-94. Zuculo, G. M., Knap, C. C. F., & Pinato, L. (2014). Correlation between sleep and quality of life in cerebral palsy. CoDAS, 26(6), 447-456. 台灣版世界衛生組織生活品質問卷發展小組 (民89)。台灣版世界衛生組織生活品質問卷之發展簡介。中華醫誌,19,315-324。 姚開屏(民91)。台灣版世界衛生組織生活品質問卷之發展與應用。中華醫誌,6 (3), 193-200。 | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/50185 | - |
| dc.description.abstract | 研究目的:腦性麻痺青少年生活品質量表在英語系國家已被用以評估腦性麻痺青少年的生活品質相關問題。本研究將腦性麻痺青少年生活品質量表翻譯為中文版本並且檢驗其心理計量特性,並進一步使用中文版腦性麻痺青少年生活品質量表來探討家長和腦性麻痺青少年對於自評測驗的一致性。
研究方法:此研究將腦性麻痺青少年生活品質量表翻譯為中文版本,並由三位職能治療專業專家進行內容效度審核。113位13至18歲腦性麻痺青少年(平均年齡15.6歲,標準差1.54,75 位男性青少年,38 位女性青少年)及58位主要照顧者(7位父親,45位母親,1位祖父母,5位其他) 有效填答中文版腦性麻痺青少年生活品質量表自評量表及主要照顧者量表。內部一致性取樣樣本自青少年自填版本以及主要照顧者版本,再測信度間隔四個星期並取樣17位腦性麻痺青少年及其主要照顧者。效標效度則是比較腦性麻痺青少年生活品質量表的七個領域與台灣簡明版生活品質問卷各範疇。建構效度則是使用探索性因素分析來檢驗原版腦性麻痺青少年生活品質量表的重要因素。 結果:中文版腦性麻痺青少年生活品質量表具備可高度的內部一致性(Cronbach’s α=0.83 - 0.92:青少年、Cronbach’s α= 0.76 -0.92:主要照顧者)、再測信度為中度到高度相關(青少年自填版本:CCs= 0.46- 0.96,主要照顧者版本之再測信度:ICCs= 0.27- 0.92)。探索性因素分析顯示各項目在中文版本中僅有兩個因子,與台灣簡明版世界衛生組織生活品質問卷比較之效標效度為低度到中度相關 (rs = 0.232-0.640)。施測中文版腦性麻痺青少年生活品質量表的青少年及其主要照顧者對於生活品質的 看法呈現中度一致性 (ICCs= 0.53-0.70)。 結論:本研究結果顯示,中文版腦性麻痺青少年生活品質量表是一個具有良好信效度用以評估生活品質的評量工具,適用於評量台灣及中文語系的腦性麻痺青少年之生活品質。 | zh_TW |
| dc.description.abstract | Purpose: Health-related quality of life (HRQoL) has been attracting attention of clinicians working with children with the adolescents with Cerebral Palsy (CP). It is of great importance to provide clinicians a well-developed measurement for assessing the HRQoL of the adolescents with CP..The present study is aimed to cross culturally translate the Cerebral Palsy Quality of Life questionnaire-for adolescents (CPQOL-Teen) into Mandarin Chinese and evaluate its psychometric properties when used in Taiwanese Adolescents with CP.
Methods: The study was conducted in two phases. In Phases one, four steps were followed, i.e, 1) forward translation of the CPQOL-Teen according to guidelines developed by Beton, Bombardier, Guilemin, and Feraz (2000) for cross-cultural adaptation of instruments by a committee, 2) expert evaluation of the translation, 3) blind back-translation, and 4) pilot testing and cognitive interviewing. In Phase II, the evaluation of the psychometric properties of the Chinese version of the CPQOL-Teen was conducted. The Chinese version of the CPQOL-Teen was administered to 113 adolescents with CP along with 58 primary caregivers from a medical center, a special school for children and adolescents with CP, senior and junior high schools in Greater Taipei area and long-term care facilities in Taiwan. Internal consistency was examined by using Cronbach alpha, item- subscale correlations by Pearson correlation, test-retest reliability by intraclass correlation (ICC). In addition, content validity was investigated by expert validation, construct validity by both confirmatory and exploratory factor analyses. Criterion-related validity were evaluated by the correlation of the CP-QOL Teen with the WHOQOL BREF Taiwan version using ICC. Agreement between the adolescents with their primary caregivers was also investigated by ICC.. Results: A total of 113 adolescents with CP aged thirteen to eighteen years (mean age = 15.6 years, SD = 1.54, 75 males, 38 females) along with fifty-eight primary caregivers (7 fathers, 45 mothers, 1 grandparent, 5 other caregivers) completed the Chinese version CPQOL-Teen questionnaire. The Chinese version of the CPQOL-Teen demonstrated acceptable to good internal consistency (Cronbach’s αs= 0.83 -0.92: adolescent self- report version; Cronbach’s αs = 0.76- 0.92: primary caregiver version), moderate to good test-retest reliability for adolescent self-report (ICCs= 0.49- 0.96), and poor to good test-retest reliability for primary caregiver version (ICCs= 0.27 - 0.92). Most correlations (Self report: General wellbeing and participation: 0.42-0.77, Communication and physical health: 0.43-0.77, School wellbeing: 0.62-0.80, Social wellbeing: 0.54-0.83, Feeling with functioning: 0.70- 0.83; Primary caregiver report: General wellbeing and participation: 0.52-0.80, Communication and physical health: 0.50-0.75, School wellbeing: 0.68-0.86, Social wellbeing: 0.64-0.82, Feeling with functioning: 0.55- 0.84, Access to service: 0.20-0.89, Family health: 0.84-0.93) were higher between items and subscales of the original English version than those with other subscales. Exploratory factor analysis of the Chinese version CPQOL-Teen resulted in a two- factors pattern. Concurrent validity with the WHOQOL-BREF Taiwan version showed poor to moderate (0.232-0.640) subscales correlations. Agreement between the adolescents and primary caregivers was moderate (0.53-0.70). Conclusions: Results of the study suggest that the Chinese version CPQOL-Teen is c a reliable and valid instrument for evaluating adolescents with CP’s HRQoL in Taiwan. Agreement between adolescents with CP and their primary caregiver showed moderate correlation. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T12:31:56Z (GMT). No. of bitstreams: 1 ntu-105-R02429008-1.pdf: 2561769 bytes, checksum: 03e10ec684972f8f672e51cabd4bfbe4 (MD5) Previous issue date: 2016 | en |
| dc.description.tableofcontents | 中文摘要 i
ABSTRACT iii Chapter 1 Introduction 1 1.1 Background 1 Chapter 2 Literature Review 6 2.1 Cerebral Palsy 6 2.1.1 Definition and prevalence of cerebral palsy 6 2.2 Classification of cerebral palsy 6 2.3 Limitations of individual with cerebral palsy according to International Classification of Functioning, Disability and Health- Children & Youth version (ICF-CY) 9 2.3.1 Introduction to the International Classification of Functioning, Disability and Health- Children & Youth version (ICF-CY) 9 2.3.2 The core sets of International Classification of Functioning, Disability and Health- Children & Youth version (ICF-CY) of adolescents with cerebral palsy 10 2.4 Health-Related Quality of life 11 2.4.1 Types of health-related quality of life (HRQoL) measurements 12 2.4.1.1 Generic and condition-specific HRQoL measurement 12 2.4.1.2 Self-report and primary caregiver proxy report of health-related quality of life 13 2.4.2 Health-related quality of life of adolescent with cerebral palsy 13 2.4.2.1 Primary caregiver/parent version and self-report of HRQoL in adolescent with cerebral palsy 15 2.5 Commonly used condition-specific measures of quality of life use in adolescents with cerebral palsy 17 2.5.1 Cerebral Palsy Quality of Life Questionnaire for Adolescents (CPQOL-Teen) 18 2.5.2 DISABKIDS CP modules 18 2.5.3 Caregiver Priorities and Child Health Index of Life with Disabilities (CPCHILD) 19 2.5.4 Pediatric Quality of Life Inventory 3.0 CP module (PedsQL-CP 3.0) 20 2.5.5 Lifestyle Assessment Questionnaire-CP parent version (LAQ-CP) 21 2.5.6 Care & comfort hypertonicity Questionnaire (CCHQ) 22 2.5.7 Pediatric Outcomes Data Collection Instrument (PODCI) 22 2.6 Limitations of the existing HRQoL measures for adolescents with CP 23 2.7 Summary of literature review 25 2.8 Purpose of this study 26 CHAPTER 3 Phase I: Translation and cultural adaptation process of the CPQOL-Teen 27 3.1Measures 27 3.2 Procedures and Results 28 CHAPTER 4 Phase II: Evaluation of the psychometric properties of the Cerebral Palsy Quality of life for Adolescents Chinese version (the CPQOL-Teen-C) 31 4.1 Participants 31 4.1.1Adolescents with cerebral palsy 31 4.1.2 Parents and/ or primary caregivers of adolescents with cerebral palsy (CP) 31 4.2 Measures 32 4.2.1 The Chinese version of the Cerebral Palsy Quality of life for Adolescents (CPQOL-Teen) 32 4.2.2World Health Organization Quality of life-BREF (WHOQOL-BREF Taiwan version) 32 4.2.3 Gross Motor Function Classification Scale (GMFCS) 33 4.2.4 Life events 33 4.3 Procedures 34 4.4 Statistical analysis 34 4.4.1 Demographic data analysis 35 4.4.2 Internal consistency 35 4.4.3 Item- subscale correlations 35 4.4.4 Test- retest reliability 35 4.4.5 Agreement between the perspectives of adolescents and primary caregivers 36 4.4.6 Construct validity 36 4.4.7 Concurrent validity 37 4.5 Results 37 4.5.1 Demographics of adolescents with CP and primary caregivers 37 4.5.2 The effect of gender and GMFCS levels on HRQOL 38 4.5.3 Reliability 38 4.5.3.1 Internal consistency 38 4.5.3.2 Item- subscale correlations 38 4.5.3.3 Test-retest reliability 40 4. 5.4 Validity 41 4. 5.4.1 Content validity 41 4.5.4.2 Construct validity 42 4.5.4.2.1 Exploratory Factor Analysis 42 4.5.4.3 Concurrent validity 43 CHAPTER 5 Discussion 44 5.1 Gender and GMFCS differences 44 5.2 Reliability 45 5.3 Validity 47 5.4 Agreement between self-report version and primary caregiver version 48 5.5 Limitations 49 CHAPTER 6 Conclusion 51 References 52 | |
| dc.language.iso | en | |
| dc.subject | 青少年 | zh_TW |
| dc.subject | 腦性麻痺 | zh_TW |
| dc.subject | 兒童職能治療 | zh_TW |
| dc.subject | 自評 | zh_TW |
| dc.subject | 健康相關生活品質 | zh_TW |
| dc.subject | 青少年 | zh_TW |
| dc.subject | 腦性麻痺 | zh_TW |
| dc.subject | 健康相關生活品質 | zh_TW |
| dc.subject | 自評 | zh_TW |
| dc.subject | 兒童職能治療 | zh_TW |
| dc.subject | pediatric occupational therapy | en |
| dc.subject | cerebral palsy | en |
| dc.subject | adolescent | en |
| dc.subject | HRQoL | en |
| dc.subject | self-report | en |
| dc.subject | pediatric occupational therapy | en |
| dc.subject | cerebral palsy | en |
| dc.subject | adolescent | en |
| dc.subject | HRQoL | en |
| dc.subject | self-report | en |
| dc.title | 腦性麻痺青少年生活品質量表中文版之信效度探討 | zh_TW |
| dc.title | Psychometric properties of a Chinese version of the Cerebral Palsy Quality of Life Questionnaire-for Adolescents (CPQOL-Teen) in teenagers with cerebral palsy in Taiwan | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 104-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 姚開屏(Kaiping- Grace Yao),陳官琳(Kuan-Lin Chen) | |
| dc.subject.keyword | 腦性麻痺,青少年,健康相關生活品質,自評,兒童職能治療, | zh_TW |
| dc.subject.keyword | cerebral palsy,adolescent,HRQoL,self-report,pediatric occupational therapy, | en |
| dc.relation.page | 127 | |
| dc.identifier.doi | 10.6342/NTU201601793 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2016-08-04 | |
| dc.contributor.author-college | 醫學院 | zh_TW |
| dc.contributor.author-dept | 職能治療研究所 | zh_TW |
| 顯示於系所單位: | 職能治療學系 | |
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