Effects of a Personalized Physical Training to Reduce Fatigue (NCT05899595) | Clinical Trial Compass
TerminatedNot Applicable
Effects of a Personalized Physical Training to Reduce Fatigue
Stopped: end of thesis funding
France101 participantsStarted 2023-09-27
Plain-language summary
Chronic fatigue (CF) is a pathological fatigue over at least 6 months, without improvement after rest or sleep. In primary care, it is the major complaint in 5 to 10% of the consultations. Physical activity is an efficient therapy to help reducing this fatigue in addition to the improvement of muscular and cardiorespiratory functions. However, it remains little exploited. Yet the studies focus mainly on precise chronic pathologies with general trainings, without considering the fatigue status and reveal a large heterogeneity. Personalizing the physical training appears to be the next step in order to improve chronic fatigue patients care.
The objective of this study will be to investigate the relevance and the effects of a personalized physical training to reduce fatigue in chronic fatigue patients.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
The primary outcome is the change in the FACIT-F score obtained before and after the exercise procedure.
Timeframe: Month 1, 4
Trial details
NCT IDNCT05899595
SponsorCentre Hospitalier Universitaire de Saint Etienne