The development of a new measure of quality of life for children with congenital cardiac disease

Susan Macran, Yvonne Birks, Jonathan Parsons, Patricia Sloper, Geoff Hardman, Paul Kind, Carin van Doorn, David, R. Thompson , Robert Lewin*

*Corresponding author for this work

Research output: Contribution to journalArticle

33 Citations (Scopus)


The purpose of the study was to develop a questionnaire measuring health-related R1 quality of life for children and adolescents with congenital heart disease, the ConQol, that would have both clinical and research applications. We describe here the process of construction of a questionnaire, the piloting and the development of a weighted scoring system, and data on the psychometric performance of the measure in a sample of 640 children and young people recruited via 6 regional centres for paediatric cardiology from across the United Kingdom. The ConQol has two versions, one designed for children aged from 8 to 11 years, and the other for young people aged from 12 to 16 years. Initial findings suggest that it is a valid and reliable instrument, is acceptable to respondents, and is simple to administer in both a research and clinical context.

Original languageEnglish
Pages (from-to)165-172
Number of pages8
JournalCardiology in the Young
Issue number2
Publication statusPublished - 01 Apr 2006


  • Child
  • Congenital cardiac malformations
  • Health outcomes
  • Psychosocial

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Cardiology and Cardiovascular Medicine

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