Abstract
The Pediatric Quality of Life Inventory™ Family Impact Module (PedsQL™ FIM) is a health-related quality of life and family functioning questionnaire for parents of children with chronic conditions. The aim of this study was to develop the Croatian version of the PedsQL™ FIM and to evaluate its psychometric properties. The study included 212 parents of children with chronic gastrointestinal disorders (GID) and those of healthy children. All parents completed the PedsQL™ FIM, PedsQL™ 4.0 Generic Core Scales (PedsQL), and World Health Organization Quality of Life-BREF questionnaire (WHOQOL-BREF). The Croatian version of the PedsQL™ FIM was developed following strict procedures for the translation and cross-cultural adaptation process (i.e. forward translation, reconciliation, backward translation, and pre-testing). Psychometric analyses included testing internal consistency reliability (Cronbach’s coefficient) and aspects of construct validity (Spearman’s correlation coefficients, known-groups comparison method, and exploratory factor analysis—EFA). Cronbach’s α of 0.7 and above were found for all scales. Parents of healthy children reported significantly higher all PedsQL™ FIM scores than parents of children with GID. Correlations between the PedsQL™ FIM and WHOQOL-BREF scales ranged 0.07–0.56. The EFA found 6 factors to explain 73.79 % of the total variance. Finally, the PedsQL™ FIM correlated moderate to high (range 0.46–0.64) to all PedsQL™ scores. The measure is feasible, short, and easily scored. It has appropriate internal consistency reliability and acceptable construct validity. However, more studies about validity are needed that will include other children with chronic conditions considering that a questionnaire validation is an iterative process.
Similar content being viewed by others
References
Acquadro, C., Berzon, R., Dubois, D., Leidy, N. K., Marquis, P., Revicki, D., et al. (2003). Incorporating the patient’s perspective into drug development and communication: An Ad Hoc Task Force report on the Patient-Reported Outcomes (PRO) Harmonization Group Meeting at the Food and Drug Administration, February 16, 2001. Value in Health, 5, 522–531.
Chassany, O., Sagnier, P., Marquis, P., Fullerton, S., & Aaronson, N. (2002). Patient-reported outcomes: The example of health-related quality of life—A European guideline document for the improved integration of health-related quality of life assessment in the drug regulatory process. Drug Information Journal, 36, 209–238.
Chen, R., Hao, Y., Feng, L., Zhang, Y., & Huang, Z. (2011). The Chinese version of the Pediatric Quality of Life Inventory™ (PedsQL™) Family Impact Module: Cross-cultural adaptation and psychometric evaluation. Health and Quality of Life Outcomes, 9, 16.
Cohen, J. (1988). Statistical power analysis for the behavioral sciences (2nd ed.). Hillsdale, NJ: Lawrence Erlbaum.
Cohen, M. S. (1999). Families coping with childhood chronic illness: A research review. Families, Systems, & Health, 17(2), 149.
Eiser, C., & Morse, R. (2001). Quality-of-life measures in chronic diseases of childhood. Health Technology Assessment, 5(4), 1–157.
Field, A. (2009). Discovering statistics using SPSS (3rd ed.). London: Sage Publications Limited.
Floyd, F. J., & Widaman, K. F. (1995). Factor analysis in the development and refinement of clinical assessment instruments. Psychological assessment, 7(3), 286–299.
Goldbeck, L. (2006). The impact of newly diagnosed chronic paediatric conditions on parental quality of life. Quality of Life and Research, 15, 1121–1131.
Herdman, M., Fox-Rushby, J., & Badia, X. (1998). A model of equivalence in the cultural adaptation of HRQoL instruments: The universalist approach. Quality of life and Research, 7(4), 323–335.
Ingerski, L. M., Modi, A. C., Hood, K. K., Pai, A. L., Zeller, M., Piazza-Waggoner, C., et al. (2010). Health-related quality of life across pediatric chronic conditions. The Journal of Pediatrics, 156(4), 639–644.
Jastrowski Mano, K. E., Khan, K. A., Ladwig, R. J., & Weisman, S. J. (2011). The impact of pediatric chronic pain on parents’ health-related quality of life and family functioning: reliability and validity of the PedsQL 4.0 Family Impact Module. Journal of Pediatric Psychology, 36, 517–527.
Knez, R., Francisković, T., Samarin, R. M., & Niksić, M. (2011a). Attachment style in parents of children with chronic gastrointestinal disease. Collegium Antropolgicum, 35(Suppl 2), 125–130.
Knez, R., Francisković, T., Samarin, R. M., & Niksić, M. (2011b). Parental quality of life in the framework of paediatric chronic gastrointestinal disease. Collegium Antropolgicum, 35(Suppl 2), 275–280.
Mazaheri MM, Rae-Seebach RD, Preston HE, Schmidt M, Field N, Cassidy S, Packman W. (2012). The impact of Prader–Willi syndrome on the family’s quality of life and caregiving, and the unaffected siblings’ psychosocial adjustment. Journal of Intellectual Disability Research. doi:10.1111/j.1365-2788.2012.01634.x.
McGrath-Morrow, S.A., Ryan, T., Riekert, K., Lefton-Greif, MA, Eakin M, & Collaco JM. (2012). The impact of bronchopulmonary dysplasia on caregiver health related quality of life during the first 2 years of life. Pediatric Pulmology. doi:10.1002/ppul.22687.
Medrano, G. R., Berlin, K. S., & Davies, W. H. (2013). Utility of the PedsQL™ family impact module: assessing the psychometric properties in a community sample. Quality of Life and Research. doi:10.1007/s11136-013-0422-9.
Nunnally, J. C., & Bernstein, I. R. (1994). Psychometric theory. New York: McGraw-Hill.
Panepinto, J. A., Hoffmann, R. G., & Pajewski, N. M. (2009). A psychometric evaluation of the PedsQL Family Impact Module in parents of children with sickle cell disease. Health and Quality of Life Outcomes, 7, 32.
Quittner, A. L., Espelage, D. L., Opipari, L. C., Carter, B., Eid, N., & Eigen, H. (1998). Role strain in couples with and without a child with a chronic illness: Associations with marital satisfaction, intimacy, and daily mood. Health Psychology, 17(2), 112.
Rahman, A. A., Mohamad, N., Imran, M. K., Ibrahim, W. P., Othman, A., Aziz, A. A., et al. (2011). A preliminary study on the reliability of the Malay Version of PedsQL™ Family Impact Module among caregivers of children with disabilities in Kelantan, Malaysia. Malaysian Journal of Medical Science, 18, 63–68.
Ravens-Sieberer, U., Erhart, M., Wille, N., Wetzel, R., Nickel, J., & Bullinger, M. (2006). Generic Health-related Quality of life assessment in children and adolescents: Methodological considerations. Pharmacoeconomics, 24(12), 1199–1220.
Scarpelli, A. C., Paiva, S. M., Pordeus, I. A., Varni, J. W., Viegas, C. M., & Allison, P. J. (2008). The pediatric quality of life inventory (PedsQL) family impact module: Reliability and validity of the Brazilian version. Health and Quality of Life Outcomes, 6, 35.
Silver, E. J., Westbrook, L. E., & Stein, R. E. (1998). Relationship of parental psychological distress to consequences of chronic health conditions in children. Journal of Pediatric Psychology, 23(1), 5–15.
Streiner, D. (2003). Starting at the beginning: an introduction to coefficient alpha and internal consistency. Journal of Personality Assessment, 80, 99–103.
Terwee, C. B., Bot, S. D., de Boer, M. R., van der Windt, D. L. A., Knol, D. L., Dekker, J., et al. (2007). Quality criteria were proposed for measurement properties of health status questionnaires. Journal of Clinical Epidemiology, 60(1), 34–42.
The WHOQOL Group. (1998). WHOQOL user manual. Geneva: WHO.
Turkel, S., & Pao, M. (2007). Late consequences of chronic pediatric illness. Psychiatric Clinics of North America, 30(4), 819–835.
Van Cleave, J., Gortmaker, S. L., & Perrin, J. M. (2010). Dynamics of obesity and chronic health conditions among children and youth. JAMA: The Journal of the American Medical Association, 303(7), 623–630.
van der Lee, J. H., Mokkink, L. B., Grootenhuis, M. A., Heymans, H. S., & Offringa, M. (2007). Definitions and measurement of chronic health conditions in childhood. JAMA: the journal of the American Medical Association, 297(24), 2741–2751.
Varni, J. W., Burwinkle, T. M., & Lane, M. M. (2005). Health-related quality of life measurement in pediatric clinical practice: An appraisal and precept for future research and application. Health and Quality of Life Outcomes, 3(1), 34.
Varni, J., Limbers, C., & Burwinkle, T. (2007a). Impaired health-related quality of life in children and adolescents with chronic conditions: A comparative analysis of 10 disease clusters and 33 disease categories/severities utilizing the PedsQL™ 4.0 Generic Core Scales. Health and Quality of Life Outcomes, 5(1), 43.
Varni, J. W., Limbers, C., & Burwinkle, T. M. (2007b). Literature review: health-related quality of life measurement in pediatric oncology: Hearing the voices of the children. Journal of Pediatric Psychology, 32(9), 1151–1163.
Varni, J. W., Seid, M., & Kurtin, P. S. (2001). PedsQL 4.0TM: Reliability and validity of the pediatric quality of life inventory TM version 4.0 Generic Core Scales in healthy and patient populations. Medical Care, 39, 800–812.
Varni, J. W., Seid, M., & Rode, C. A. (1999). The PedsQL™: Measurement model for the pediatric quality of life inventory. Medical Care, 37, 126–139.
Varni, J. W., Sherman, S. A., Burwinkle, T. M., Dickinson, P. E., & Dixon, P. (2004). The PedsQL family impact module: Preliminary reliability and validity. Health and Quality of Life Outcomes, 2, 55.
Wallander, J. L., & Varni, J. W. (1998). Effects of pediatric chronic physical disorders on child and family adjustment. Journal of Child Psychology and Psychiatry, 39, 29–46.
Wamboldt, M. Z., & Wamboldt, F. S. (2000). Role of the family in the onset and outcome of childhood disorders: Selected research findings. Journal of the American Academy of Child and Adolescent Psychiatry, 39(10), 1212–1219.
World Health Organization. (2007). International classification of functioning, disability, and health: Children and youth version: ICF-CY. Geneva: WHO.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Knez, R., Stevanovic, D., Vulić-Prtorić, A. et al. The Croatian Version of the Pediatric Quality of Life Inventory (PedsQL™) Family Impact Module: Cross-Cultural Adaptation and Psychometric Evaluation. J Child Fam Stud 24, 363–371 (2015). https://doi.org/10.1007/s10826-013-9844-9
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10826-013-9844-9