Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis

Alexandra L. Quittner, Sheri Sweeny, Marc Watrous, Paul Munzenberger, Karen Bearss, Amy Gibson Nitza, Lisa A. Fisher, Bernadette Henry

Research output: Contribution to journalArticle

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Abstract

Objective: To develop a conceptually and semantically valid English version of a French disease-specific measure of quality of life for children, adolescents, and adults with cystic fibrosis (CF). Methods: Following a backward and forward translation of the measure, 60 participants, including 20 children, 20 parents, and 20 adolescents/young adults completed the Cystic Fibrosis Questionnaire (CFQ) and a series of cognitive probes evaluating their understanding of the items and response choices. Results: Semantic and conceptual problems with the items were identified and modified for the second set of cognitive interviews. Response distributions across items and ages were adequate, and the predicted associations between disease severity and quality of life were obtained. Conclusions: The English version of the CFQ appears to be a linguistically valid measure of quality of life for patients with CF. A national validation study is now under way to test the psychometric properties of the measure.

Original languageEnglish (US)
Pages (from-to)403-414
Number of pages12
JournalJournal of pediatric psychology
Volume25
Issue number6
StatePublished - Oct 9 2000

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Keywords

  • Cystic fibrosis
  • Methodology
  • Pediatric psychology
  • Quality of life

ASJC Scopus subject areas

  • Psychology(all)
  • Developmental and Educational Psychology

Cite this

Quittner, A. L., Sweeny, S., Watrous, M., Munzenberger, P., Bearss, K., Nitza, A. G., Fisher, L. A., & Henry, B. (2000). Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis. Journal of pediatric psychology, 25(6), 403-414.