Active — Not RecruitingNot Applicable

Efficiency of an Optimized Care Organization for Fibromyalgia Patients. The FIMOUV 2 Study

France330 participantsStarted 2020-01-23

Plain-language summary

Fibromyalgia affects 2 to 5% of adults in the general population. Patients describe a combination of symptoms centred around fatigue not induced by exercise and not relieved by rest. The diagnosis of fibromyalgia is self-perpetuating by the deconditioning, consequence of a reduced muscle mass due to inactivity and periods of prolonged rest. Thus, it seems fundamental to develop other non-drug approaches: among them, adapted physical activity is recommended by most learned societies because of a good level of evidence (Level 1, Grade A). The question remains, however, whether simple advice to resume physical activity is sufficient (routine care with medical assessment at 3 months) or whether a physical activity supervised inside and outside the hospital is not more relevant.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Patient diagnosed with fibromyalgia according to ACR (American College of rheumatology) criteria (total score WPI (Widespread Pain Index) + SS (Severity Scale) ) ≥ 13 * French writing and speaking * Sedentary or low level of activity (less than 150 minutes of regular physical activity per week at the time of inclusion) * Signature of informed consent Exclusion Criteria: * Cardiac or respiratory diseases that contraindicate the practice of physical activity * Significant co-morbidities that contraindicate the practice of physical activity: associated cardiac pathologies (severe rhythm disorders such as rapid atrial fibrillation), respiratory pathologies (severe obstructive or severe respiratory insufficiency), disabling joint pathologies (knee osteoarthritis or osteoarthritis of the hip) training on a treadmill or on a high intensity bike). * Impossibility of submitting to the medical monitoring of the program for geographical, social or psychological reason

What they're measuring

physical activity

Timeframe: 12 months

Trial details

NCT IDNCT04107948

SponsorCentre Hospitalier Universitaire de Saint Etienne

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-10-01