Development, validation, and implementation of a questionnaire assessing disease knowledge and understanding in adult cystic fibrosis patients.
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Affiliation
National Referral Centre for Adult Cystic Fibrosis, St. Vincent's University, Hospital, Dublin, Ireland.Issue Date
2012-02-01T10:32:38ZMeSH
AdolescentAdult
Cystic Fibrosis/*psychology
Female
*Health Education
*Health Knowledge, Attitudes, Practice
Humans
Male
Middle Aged
Questionnaires/*standards
Reproducibility of Results
Young Adult
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J Cyst Fibros. 2010 Dec;9(6):400-5. Epub 2010 Aug 14.Journal
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis, SocietyDOI
10.1016/j.jcf.2010.07.001PubMed ID
20709606Abstract
BACKGROUND: The number of adults living with cystic fibrosis (CF) is increasing, necessitating an assessment of knowledge in this growing population. METHODS: A questionnaire assessing CF knowledge was completed by 100 CF patients (median age: 26.0 years, range 17-49 years; median FEV: 57.0% predicted, range 20-127% predicted). Level of knowledge was correlated with clinical and sociodemographic characteristics. RESULTS: Questionnaire validation showed acceptable internal consistency (alpha=0.75) and test-retest reliability (0.94). Patients had fair overall understanding of CF (mean=72.4%, SD=13.1), with greater knowledge of lung and gastrointestinal topics (mean=81.6%, SD=11.6) than reproduction and genetics topics (mean=57.9%, SD=24.1). Females and those with post-secondary education scored significantly higher (p<0.05). CONCLUSIONS: This study validated a questionnaire that can be utilized to assess CF knowledge. Although CF patients understand most aspects of their disease, knowledge deficits are common - particularly regarding genetics and reproduction - and should be considered when developing CF education programs.Language
engISSN
1873-5010 (Electronic)1569-1993 (Linking)
ae974a485f413a2113503eed53cd6c53
10.1016/j.jcf.2010.07.001
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