Feasibility, reliability and validity of the Thai version of the Pediatric Quality of Life Inventory 3.0 cerebral palsy module

Quality of Life Research

Volumn 22, Issue 2, 2013, Pages 415-421

  Tantilipikorn, Pinailug ^a,c   Watter, Pauline ^a   Prasertsukdee, Saipin ^b  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b MAHIDOL UNIVERSITY   (Thailand)

^c THAMMASAT UNIVERSITY   (Thailand)

Author keywords

Cerebral palsy; Health related quality of life (HRQOL); PedsQL; Psychometric properties; Thai

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; ASIAN; CAREGIVER; CEREBRAL PALSY; CHILD; CUSTODY; EQUIPMENT; FEASIBILITY STUDY; FEMALE; HEALTH STATUS; HUMAN; LANGUAGE; MALE; MIDDLE AGED; PARENT; PSYCHOLOGICAL ASPECT; PSYCHOMETRY; QUALITY OF LIFE; REPRODUCIBILITY; SELF CONCEPT; SELF REPORT; THAILAND; TRANSLATING (LANGUAGE); YOUNG ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; DEVICES; PROXY; PSYCHOLOGY;

ADOLESCENT; ADULT; AGED; ASIAN CONTINENTAL ANCESTRY GROUP; CAREGIVERS; CEREBRAL PALSY; CHILD; FEASIBILITY STUDIES; FEMALE; HEALTH STATUS; HUMANS; LANGUAGE; MALE; MIDDLE AGED; PARENTS; PROXY; PSYCHOMETRICS; QUALITY OF LIFE; REPRODUCIBILITY OF RESULTS; SELF CONCEPT; SELF REPORT; THAILAND; TRANSLATING; YOUNG ADULT;

EID: 84878387343     PISSN: 09629343     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11136-012-0161-3     Document Type: Article

References (22)

1. Rosenbaum, P.; Paneth, N.; Leviton, A.; Goldstein, M.; Bax, M.; Damiano, D.; et al. (2007). A report: The definition and classification of cerebral palsy April 2006. Developmental Medicine and Child Neurology Supplement, 109, 8-14.
2. Aran, A. (2010). Quality of life in children with cerebral palsy handbook of disease burdens and quality of life measures. In V. R. Preedy, & R. R. Watson (Eds.), pp. 2453-2468. New York: Springer.
3. McCullough, N.; & Parkes, J. (2008). Use of the child health questionnaire in children with cerebral palsy: A systematic review and evaluation of the psychometric properties. Journal of Pediatric Psychology, 33(1), 80-90.
4. Davis, E.; Shelly, A.; Waters, E.; & Davern, M. (2009). Measuring the quality of life of children with cerebral palsy: Comparing the conceptual differences and psychometric properties of three instruments. Developmental Medicine and Child Neurology.
5. McCarthy, M. L.; Silberstein, C. E.; Atkins, E. A.; Harryman, S. E.; Sponseller, P. D.; & Hadley-Miller, N. A. (2002). Comparing reliability and validity of pediatric instruments for measuring health and well-being of children with spastic cerebral palsy. Developmental Medicine and Child Neurology, 44(7), 468-476.
6. Waters, E.; Davis, E.; Mackinnon, A.; Boyd, R.; Graham, H. K.; Kai Lo, S.; et al. (2007). Psychometric properties of the quality of life questionnaire for children with CP. Developmental Medicine and Child Neurology, 49(1), 49-55.
7. Varni, J. W.; Burwinkle, T. M.; Berrin, S. J.; Sherman, S. A.; Artavia, K.; Malcarne, V. L.; et al. (2006). The PedsQL in pediatric cerebral palsy: reliability, validity, and sensitivity of the generic core scales and cerebral palsy module. Developmental Medicine and Child Neurology, 48(6), 442-449.
8. Yang, X.; Xiao, N.; & Yan, J. (2010). 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, 1-10.
9. http://www.pedsql.org. 6 Oct 2010.
10. Amiri, P.; Emad, M. A.; Sara, J.; Farhad, H.; James, V.; Fazlollah, G.; et al. (2010). Reliability and validity of the Iranian version of the Pediatric Quality of Life Inventory™ 4.0 generic core scales in adolescents. Quality of Life Research, 19(10), 1501-1508.
11. Varni, J. W.; & Limbers, C. A. (2009). The pediatric quality of life inventory: Measuring pediatric health-related quality of life from the perspective of children and their parents. Pediatric Clinics of North America, 56(4), 843-863.
12. Donner, A.; & Eliasziw, M. (1987). Sample size requirements for reliability studies. Statistics in Medicine, 6(4), 441-448.
13. Varni, J. W.; Seid, M.; & Kurtin, P. S. (2001). PedsQL 4.0: Reliability and validity of the Pediatric Quality of Life Inventory version 4.0 generic core scales in healthy and patient populations. Medical Care, 39(8), 800-812.
14. Lee, K. A.; & Kieckhefer, G. M. (1989). Measuring human responses using visual analogue scales. Western Journal of Nursing Research, 11(1), 128-132.
15. Beaton, D.; Bombardier, C.; Guillemin, F.; & Ferraz, M. B. (2000). Guidelines for the process of cross-cultural adaptation of self-report measures. Spine, 25, 3186-3191.
16. Gjersing, L.; Caplehorn, J. R.; & Clausen, T. (2010). Cross-cultural adaptation of research instruments: Language, setting, time and statistical considerations. BMC Medical Research Methodology, 10, 13.
17. Guillemin, F.; Bombardier, C.; & Beaton, D. (1993). Cross-cultural adaptation of health-related quality of life measures: Literature review and proposed guidelines. Journal of Clinical Epidemiology, 46(12), 1417-1432.
18. McHorney, C. A.; Ware, J. E.; Jr, Lu, J. F.; & Sherbourne, C. D. (1994). The MOS 36-item Short-Form Health Survey (SF-36): III. Tests of data quality, scaling assumptions, and reliability across diverse patient groups. Medical Care, 32(1), 40-66.
19. Varni, J. W.; Burwinkle, T. M.; Sherman, S. A.; Hanna, K.; Berrin, S. J.; Malcarne, V. L.; et al. (2005). Health-related quality of life of children and adolescents with cerebral palsy: Hearing the voices of the children. Developmental Medicine and Child Neurology, 47(9), 592-597.
20. Portney, L. G.; & Watkins, M. P. (2009). Foundations of clinical research: Applications to practice (3rd ed.; p. xix, 892). Upper Saddle River, NJ: Pearson, Prentice Hall.
21. Hair, J. F. (2006). Multivariate data analysis (6th ed.; p. xxiv, 899). Upper Saddle River, NJ: Pearson, Prentice Hall.
22. Costello, A. B.; & Osborne, J. W. (2005). Best practices in exploratory factor analysis: Four recommendations for getting the most from your analysis. Practical Assessment, Research & Evaluation, 10(7), 1-9.