Personalized physical training to reduce chronic fatigue
Effects of a Personalized Physical Training to Reduce Fatigue in Chronic Fatigue Patients: a Randomized Controlled Trial.
This study tests whether a personalized exercise program can help people with chronic fatigue feel better and have more energy.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 130 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Centre Hospitalier Universitaire de Saint Etienne Academic / other |
| Locations | 1 site (Saint-Etienne) |
| Trial ID | NCT05899595 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of a personalized physical training program designed to alleviate chronic fatigue syndrome. It aims to tailor exercise protocols to individual patients, considering their specific fatigue levels and physical capabilities. The intervention involves a structured exercise regimen that participants will follow, with the goal of improving their overall physical capacity and reducing fatigue symptoms. The study seeks to address the gap in current treatments by focusing on personalized approaches rather than generalized training methods.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who experience chronic fatigue and meet specific health criteria.
Not a fit: Patients with serious health issues that could compromise their safety during the study or those currently participating in other interventional studies may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the quality of life for patients suffering from chronic fatigue syndrome.
How similar studies have performed: While personalized training approaches are gaining attention, this specific study's focus on chronic fatigue syndrome represents a novel application in the field.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Aged ≥ 18 * Men or women * FACIT-F score ≤ 34 * Ability to walk during 10 minutes without stopping * Ability to receive the Myocene® stimulation protocol * Have given written consent * Members or beneficiaries of a social security program Exclusion Criteria: * Contraindication to experimental procedures * Important health issues that would compromise the participant security during the study * Persistent atrial fibrillation or 2nd or 3rd degree atrioventricular block * Currently participating in an other interventional study or having so in the past thirty days * Patient is pregnant * Patient is unable to give an informed consent * Patient is deprived of liberty or under guardianship
Where this trial is running
Saint-Etienne
- Centre Hospitalier de Saint-Etienne — Saint-Etienne, France (Recruiting)
Study contacts
- Principal investigator: David HUPIN, MD — Chu Saint-Etienne
- Study coordinator: David HUPIN, MD
- Email: david.hupin@chu-st-etienne.fr
- Phone: (0)477127985
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.