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Clinical Trial Summary

The purpose of this study is to understand underlying mechanisms of improved exercise tolerance in Healthy Sedentary Subjects after training program.


Clinical Trial Description

Training protocol used is based on recommendations. A minimum of 20 sessions in 4-6 weeks were proposed. The exercise intensity of exercise corresponds to target heart rate at ventilatory threshold measured during incremental exercise test. Training at this intensity allowed us to individualize effort for each patient. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT01183039
Study type Interventional
Source 5 Santé
Contact
Status Completed
Phase N/A
Start date May 2008
Completion date December 2010

See also
  Status Clinical Trial Phase
Terminated NCT00619749 - Polyphenols and Endothelial Function Phase 3