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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:

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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