Adapted physical activity program for people with anorexia nervosa
Official title: Adapted Physical Activity in the Treatment of Anorexia:
Run by Fondation Santé des Étudiants de France · NCT05477537 · Data updated 2026-11-12
This trial will test whether adding an 8-week adapted physical activity program with psychoeducation helps people with anorexia nervosa improve BMI and stay engaged in treatment.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 40 Years |
| Sex | All |
| Enrollment | 220 (estimated) |
| Sponsor | Fondation Santé des Étudiants de France Academic / other |
| Locations | 7 sites (Lille and 6 other locations) |
| Status | Recruiting |
| Started | November 14, 2023 |
| Main results expected | April 2027 |
| Study ends | April 2027 |
| Registry record updated | August 28, 2025 |
| Trial ID | NCT05477537 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
People aged 12 or older with DSM-5 anorexia nervosa who are being treated at the participating French specialized centers, can read and write French, have social coverage, and can give informed consent.
✕Probably not a fit
Patients with somatic instability requiring intensive medical care, acute psychiatric emergencies (including high suicidal risk), somatic contraindications to physical activity, inability to consent, or pregnancy/breastfeeding are unlikely to benefit or are excluded.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial adds a standardized 8-week Adapted Physical Activity (APA) program—eight 90-minute sessions combining supervised activity and psychoeducation about problematic exercise and healthy practice—to usual care for people with anorexia nervosa. Eligible participants are aged 12 or older, meet DSM-5 criteria for anorexia nervosa, and are treated in participating specialized eating-disorder centers in France. The primary outcome is change in body mass index at the end of the program, with secondary outcomes assessed at program end and six months later to measure symptoms and treatment adherence. Sessions are delivered in person and the intensity is adapted to each patient, with those medically unstable or with contraindications to exercise excluded.
Why it matters
Potential benefit: If successful, the program could allow safer, supervised inclusion of physical activity in treatment, improve BMI and reduce dropout, supporting faster recovery and less chronic illness.
How similar studies have gone: Some small trials and pilot programs of tailored exercise and psychoeducation for anorexia have shown promise for reducing hyperactivity and improving outcomes, but high-quality randomized evidence remains limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Anorexia nervosa patients (DSM 5 criteria), * over or equal to 12 years old, * Treated in the specialised eating disorder centres involved in the study either in the day hospital program or in the inpatient program, * Understanding, reading and writing French, * Benefiting from social cover * Have read the information notice and have consented to participate in the study by signing a written consent Exclusion Criteria: * Somatic instability needing intensive medical care or monitoring (intensity is adapted in each session to each patient) or psychiatric emergency (suicidal risk and/or acute psychiatric symptomatology), * Somatic complication forbidding any physical activity, * Absence social cover, * Patients in an emergency situation, incapable of giving their consent or adults under guardianship or curatorship, * Pregnant or breastfeeding women (declarative: question asked to the patient during inclusion), * Refusal to participate.
Where it's running
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Clinique Saint Vincent de Paul
Lyon, France Recruiting -
CHU Montpellier
Montpellier, France Recruiting -
CHU Nantes - service d'addictologie et Psychiatrie de Liaison
Nantes, France Recruiting -
GHU Saine Anne
Paris, France Recruiting -
UDJ Michel Ange
Paris, France Recruiting -
CHU St Etienne
Saint-Etienne, France Recruiting
Show 1 more location
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CHU Lille
Lille, France Withdrawn
Study contacts
- Study coordinator: Nathalie Godart, PU-PH
- Email: nathalie.godart@fsef.net
- Phone: 01.45.89.43.39
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.