Cystic Fibrosis Questionnaire (CFQ)

[ Authors of the CFQ version in English for the USA: A Quittner, A Buu, M Watrous, M Davis ]

Author(s)
Aussage Pierre
French CFQOL Study Group
Grosskopf Cécile
Henry Bernadette
Launois R
Purpose
  Pathology:
Congenital, hereditary, and neonatal diseases and abnormalities
Digestive system diseases
Respiratory tract diseases

  Disease:
Cystic fibrosis

  Objective:
Quality of life assessment of children, adolescents, and adults with cystic fibrosis

  Population:
Adolescent
Adult
Pediatrics
Characteristics
  Type of instrument:
Health-Related Quality of Life - HRQL (incl. health status)

  Mode of administration:
Interviewer-administered
Proxy-administered
Self-administered

[ Interviewer-administered for young children ]

  Number of items:
Child: 35; Parent (CFQ Child P): 44; Adolescent/Adult (CFQ 14+): 48 or 50 (Revised version)

  Existence of database:
No

  Time recall:
The last two weeks
 
Language(s)
  Original language:
French

  List of existing translations:
(the translations may not have undergone a full linguistic validation process. Please check status of translations with Mapi Research Trust / the developers / copyright holders / distributors)

CFQ:

German

CFQ-R:

 Danish
 German for Austria
 Polish
 Spanish for Latin America
 Dutch
 Italian
 Portuguese
 
 English for the USA
 
 
 

 


Last update: October 2009
Last update in collaboration with the author: June 2004


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