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Clinical Trial Summary

The purpose of this study is to investigate the effects of a training program in patients that have suffered a COVID infection


Clinical Trial Description

Once patients have been selected and meet inclusion criteria, they will sign informed consent. They will make a first visit to obtain the basal parameters. Once done, they will start the individualized training program for 12 weeks 3 times a week. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05307562
Study type Interventional
Source Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta
Contact
Status Active, not recruiting
Phase N/A
Start date August 10, 2021
Completion date December 2025

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