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Clinical Trial Summary

The purpose of this study is to test the impact of a personalized, partly supervised rehabilitation program on the exercise capacity in patients with pulmonary hypertension. The rehabilitation program consists of 2 weeks inpatient, 2 weeks ambulatory and 11 weeks home based rehabilitation.


Clinical Trial Description

The present study is a 15 weeks, randomized (1:1) controlled trial. Patients in both groups will not change their usual medical treatment. After 2 clinical visits (screening and randomization visit), patients in the intervention group will follow a 15 week rehabilitation program consisting of 2 weeks inpatient, 2 weeks outpatient and 11 weeks home based rehabilitation. At the end of the outpatient rehabilitation phase (week 4) and the home-based program (week 15), clinical outcomes will be reassessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03955016
Study type Interventional
Source KU Leuven
Contact Wim Janssens, Prof
Phone 0032 16 34 68 33
Email wim.janssens@uzleuven.be
Status Recruiting
Phase N/A
Start date November 13, 2018
Completion date November 1, 2020

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