Actively Recruiting
Effect of Time of Exercise Re-training on Functional Capacity in Individuals With Chronic Obstructive Pulmonary Disease (COPD)
Led by Michaël RACODON · Updated on 2026-01-12
90
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Respiratory diseases pose a major health challenge and are a leading cause of death in developed countries. Pulmonary rehabilitation (PR) is a well-established treatment that helps reduce hospital readmissions, secondary events, and mortality in patients with respiratory diseases such as chronic obstructive pulmonary disease (COPD). This research investigates how the timing of exercise re-training, specifically the time of day when patients exercise, affects their functional capacity and overall recovery. The study compares two groups of patients undergoing pulmonary rehabilitation, with one group performing endurance and muscular exercises in the morning (around 9:00 am or 9:45 am) and the other group exercising in the afternoon (between 3:00 pm and 3:45 pm). The rehabilitation program includes exercise re-training combined with therapeutic patient education, delivered under medical supervision in dedicated centers. Participants complete at least 18 rehabilitation sessions over four weeks. Participants will be assessed through various tests including a 6-minute walk test to measure functional capacity, as well as tests for endurance, muscle strength, balance, anxiety and depression, and sleep quality. These assessments help researchers evaluate how exercise timing influences physical and mental health outcomes. The trial is randomized without masking and is led by Michaël Racodon, with participant involvement lasting throughout the rehabilitation period.
CONDITIONS
Brief Title
Time of Exercise Re-training With Chronic Obstructive Pulmonary Disease (COPD)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosis of chronic obstructive pulmonary disease (COPD)
- Registered for respiratory re-education and rehabilitation at the Clinique de la Mitterie
- Able to attend at least 18 rehabilitation sessions over 4 weeks
- Signed written informed consent
- Membership of a social security system
You will not qualify if you...
- Cardiovascular contraindications to exercise
- Unstable respiratory status, including uncompensated respiratory acidosis
- Conditions interfering with pulmonary rehabilitation, such as progressive neuromuscular disease or psychiatric illness
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 4 weeks
Participants engage in pulmonary rehabilitation, which includes exercise re-training and therapeutic patient education supervised by medical professionals.
At least 18 rehabilitation sessions over 4 weeks
Trial Site Locations
Total: 1 location
1
Clinique la Mitterie
Lille, France, 59130
Actively Recruiting
Research Team
M
Michaël RACODON, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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