Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults

Peter H Klijn, Henk F van Stel, Alexandra L Quittner, Janjaap van der Net, Wytze Doeleman, Cees van der Schans, Cornelis K van der Ent

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BACKGROUND: This study assesses the reliability and validity of the Dutch version of a disease-specific measure of health-related quality of life (HRQOL) for adolescents and adults with CF (CFQ-14+). The 47-item CFQ-14+ covers nine domains, three symptom scales and one health perception scale.

METHODS: To assess psychometric characteristics of the CFQ-14+, cross-sectional (homogeneity, discriminative and construct validity) and test-retest designs were used. Eighty-four adolescents and adults with CF (mean age: 21.4 years, range 14.0-46.5 years) and a wide range of lung function (mean FEV1: 59.9% predicted, range 15-121%) completed the questionnaire during a routine visit.

RESULTS: Internal consistency was acceptable for most domains of the CFQ-14+ (alpha = 0.43-0.92) and test-retest reliability was high for all domain scores (0.72-0.98). Several domains of the CFQ-14+ were able to differentiate between individuals with varying disease severity and between nourished and malnourished patients. Construct validity of the questionnaire was fair, with moderate to strong correlation between physically orientated domains and pulmonary function (rs = 0.36-0.62).

CONCLUSION: The results demonstrate that the CFQ-14+ questionnaire is a well-validated measure of HRQOL assessment in adolescents and adults with CF.

Original languageEnglish
Pages (from-to)29-36
Number of pages8
JournalJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
Volume3
Issue number1
DOIs
Publication statusPublished - Mar 2004
Externally publishedYes

Keywords

  • adolescents
  • adults
  • age factors
  • cystic fibrosis
  • middle aged
  • quality of life
  • risk assessment
  • sex factors

Cite this

Klijn, Peter H ; van Stel, Henk F ; Quittner, Alexandra L ; van der Net, Janjaap ; Doeleman, Wytze ; van der Schans, Cees ; van der Ent, Cornelis K. / Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults. In: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 2004 ; Vol. 3, No. 1. pp. 29-36.
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title = "Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults",
abstract = "BACKGROUND: This study assesses the reliability and validity of the Dutch version of a disease-specific measure of health-related quality of life (HRQOL) for adolescents and adults with CF (CFQ-14+). The 47-item CFQ-14+ covers nine domains, three symptom scales and one health perception scale.METHODS: To assess psychometric characteristics of the CFQ-14+, cross-sectional (homogeneity, discriminative and construct validity) and test-retest designs were used. Eighty-four adolescents and adults with CF (mean age: 21.4 years, range 14.0-46.5 years) and a wide range of lung function (mean FEV1: 59.9{\%} predicted, range 15-121{\%}) completed the questionnaire during a routine visit.RESULTS: Internal consistency was acceptable for most domains of the CFQ-14+ (alpha = 0.43-0.92) and test-retest reliability was high for all domain scores (0.72-0.98). Several domains of the CFQ-14+ were able to differentiate between individuals with varying disease severity and between nourished and malnourished patients. Construct validity of the questionnaire was fair, with moderate to strong correlation between physically orientated domains and pulmonary function (rs = 0.36-0.62).CONCLUSION: The results demonstrate that the CFQ-14+ questionnaire is a well-validated measure of HRQOL assessment in adolescents and adults with CF.",
keywords = "adolescents, adults, age factors, cystic fibrosis, middle aged, quality of life, risk assessment, sex factors, fysiologie, psychologie, adolescenten, volwassenen, leeftijdsfactoren, cross-sectionele studies, cystic fibrosis, kwaliteit van leven, risicoanalyse, sensitiviteit , sekse factoren",
author = "Klijn, {Peter H} and {van Stel}, {Henk F} and Quittner, {Alexandra L} and {van der Net}, Janjaap and Wytze Doeleman and {van der Schans}, Cees and {van der Ent}, {Cornelis K}",
year = "2004",
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Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults. / Klijn, Peter H; van Stel, Henk F; Quittner, Alexandra L; van der Net, Janjaap; Doeleman, Wytze; van der Schans, Cees; van der Ent, Cornelis K.

In: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, Vol. 3, No. 1, 03.2004, p. 29-36.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Validation of the Dutch cystic fibrosis questionnaire (CFQ) in adolescents and adults

AU - Klijn, Peter H

AU - van Stel, Henk F

AU - Quittner, Alexandra L

AU - van der Net, Janjaap

AU - Doeleman, Wytze

AU - van der Schans, Cees

AU - van der Ent, Cornelis K

PY - 2004/3

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N2 - BACKGROUND: This study assesses the reliability and validity of the Dutch version of a disease-specific measure of health-related quality of life (HRQOL) for adolescents and adults with CF (CFQ-14+). The 47-item CFQ-14+ covers nine domains, three symptom scales and one health perception scale.METHODS: To assess psychometric characteristics of the CFQ-14+, cross-sectional (homogeneity, discriminative and construct validity) and test-retest designs were used. Eighty-four adolescents and adults with CF (mean age: 21.4 years, range 14.0-46.5 years) and a wide range of lung function (mean FEV1: 59.9% predicted, range 15-121%) completed the questionnaire during a routine visit.RESULTS: Internal consistency was acceptable for most domains of the CFQ-14+ (alpha = 0.43-0.92) and test-retest reliability was high for all domain scores (0.72-0.98). Several domains of the CFQ-14+ were able to differentiate between individuals with varying disease severity and between nourished and malnourished patients. Construct validity of the questionnaire was fair, with moderate to strong correlation between physically orientated domains and pulmonary function (rs = 0.36-0.62).CONCLUSION: The results demonstrate that the CFQ-14+ questionnaire is a well-validated measure of HRQOL assessment in adolescents and adults with CF.

AB - BACKGROUND: This study assesses the reliability and validity of the Dutch version of a disease-specific measure of health-related quality of life (HRQOL) for adolescents and adults with CF (CFQ-14+). The 47-item CFQ-14+ covers nine domains, three symptom scales and one health perception scale.METHODS: To assess psychometric characteristics of the CFQ-14+, cross-sectional (homogeneity, discriminative and construct validity) and test-retest designs were used. Eighty-four adolescents and adults with CF (mean age: 21.4 years, range 14.0-46.5 years) and a wide range of lung function (mean FEV1: 59.9% predicted, range 15-121%) completed the questionnaire during a routine visit.RESULTS: Internal consistency was acceptable for most domains of the CFQ-14+ (alpha = 0.43-0.92) and test-retest reliability was high for all domain scores (0.72-0.98). Several domains of the CFQ-14+ were able to differentiate between individuals with varying disease severity and between nourished and malnourished patients. Construct validity of the questionnaire was fair, with moderate to strong correlation between physically orientated domains and pulmonary function (rs = 0.36-0.62).CONCLUSION: The results demonstrate that the CFQ-14+ questionnaire is a well-validated measure of HRQOL assessment in adolescents and adults with CF.

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KW - adults

KW - age factors

KW - cystic fibrosis

KW - middle aged

KW - quality of life

KW - risk assessment

KW - sex factors

KW - fysiologie

KW - psychologie

KW - adolescenten

KW - volwassenen

KW - leeftijdsfactoren

KW - cross-sectionele studies

KW - cystic fibrosis

KW - kwaliteit van leven

KW - risicoanalyse

KW - sensitiviteit

KW - sekse factoren

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DO - 10.1016/j.jcf.2003.12.006

M3 - Article

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SP - 29

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JO - Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

JF - Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

SN - 1569-1993

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