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Clinical Trial Summary

Development, validation and evaluation of a new multimodal questionnaire to assess and quantify the abdominal involvement in patients with the inherited life shortening multi-organ disease Cystic fibrosis. In the stepwhise development of the patient reported outcome measures (PROM) repeadedly, CF-patients, their families as well as professionals working in different fields of CF-care will be included.


Clinical Trial Description

Development of a multimodal questionnaire considering the FDA guidelines for development of a PROM, the CFAbd-Score - Evaluation of reliability of the questionnaire by examining internal consistency and construct validity - Evaluation of reproducibility of the questionnaire by re-testing of patients - Assessment of cross-generational applicability of the questionnaire by sub-scoring of age groups - Evaluation of the responsiveness of the score by comparison with age-matched healthy controls - Assessment of putative relationships of abdominal symptoms with faecal inflammatory markers - Assessment of applicability of the questionnaire in other CF centers - Transfer the CFAbd-Score to other countries and languages Development and validation of a CF-specific tool for daily assessment of abdominal symptoms (patient diary), the CFAbd-day2day Development and validation of a CF-specific tool for assessment of abdominal symptoms in children < 12 years of age, the CFAbd-kid ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03052283
Study type Observational
Source Medizinische Hochschule Brandenburg Theodor Fontane
Contact Jochen G Mainz, Prof. MD
Phone +493381411803
Email jochen.mainz@mhb-fontane.de
Status Recruiting
Phase
Start date January 26, 2017
Completion date December 31, 2027

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