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Influence of a Residential Rehabilitation Program on Body Composition in Patients With Cystic Fibrosis

Cystic Fibrosis Clinical Trial

Official title:
Influence of a Residential Rehabilitation Program on Body Composition in Patients With Cystic Fibrosis (Children and Adults)

Clinical Trial Summary

The aim is to evaluate the impact of a 3-week lasting residential rehabilitation program for patients with cystic fibrosis on their nutritional status measured as BMI and body composition and pulmonary function.

Clinical Trial Description

Cystic fibrosis Patients following a residential rehabilitation program consisting of dietary adaptation, physical therapy for airway drainage and supervised inhalation therapy and physical activity for at least 3 weeks are asked to participate. Weight, height, body composition and pulmonary function will be measured at start and end of the program. Dietary intake during the program is calculated based on a 2 day weighed intake diary and physical activity will be measured with the "SenseWear pro 3" armband. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04527796
Study type Observational
Source University Hospital, Ghent
Contact
Status Terminated
Phase
Start date September 1, 2018
Completion date July 1, 2020
View Details
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