Actively Recruiting
Adapted Physical Activity Program Added to Usual Care for Anorexia Nervosa Treatment
Led by Fondation Santé des Étudiants de France · Updated on 2025-08-28
220
Participants Needed
7
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the effect of adding an 8-week standardized Adapted Physical Activity (APA) program to usual care for people with anorexia nervosa. Anorexia nervosa patients often engage in excessive physical activity, which can interfere with nutrition and cause health complications. The study hypothesizes that including the APA program, which incorporates psychoeducation about problematic physical activity and healthy exercise habits, will improve treatment outcomes such as body mass index and overall health. Participants will be randomly assigned to one of two groups: one receiving the usual treatment for anorexia nervosa in day hospital or inpatient programs according to HAS guidelines, and the other receiving the same usual care plus the APA program. The APA involves eight weekly sessions of 1.5 hours each, focusing on adapted physical activity and psychoeducation to promote safe exercise practices. The program is designed to improve treatment adherence and reduce conflicts related to physical activity restrictions. During the study, participants will be assessed at the start and end of the 9-week program, as well as 6 months later. Evaluations will include body mass index changes, body composition by bioelectric impedance, physical activity levels, fitness perception, self-esteem, body shape perception, quality of life, symptoms of anxiety, depression, and eating disorders, and treatment dropout rates. These assessments involve questionnaires, physical tests, and monitoring of physical activity. The total participation includes the 8-week program plus follow-up assessments to observe lasting effects.
CONDITIONS
Brief Title
Adapted Physical Activity in the Treatment of Anorexia:
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of anorexia nervosa according to DSM 5 criteria
- Age 12 years or older
- Receiving treatment in specialized eating disorder centers in day hospital or inpatient programs
- Ability to understand, read, and write French
- Have social health coverage
- Provided written informed consent to participate
You will not qualify if you...
- Medical instability requiring intensive care or monitoring
- Psychiatric emergency including suicidal risk or acute symptoms
- Medical complications preventing any physical activity
- Lack of social health coverage
- Emergency situations preventing consent, or adults under guardianship or curatorship
- Pregnant or breastfeeding women
- Refusal to participate
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 - 8 weeks
Participants receive treatment as usual for anorexia nervosa. Some participants also attend an adapted physical activity program with one lesson per week for 8 weeks, including psychoeducation on physical activity practices and consequences.
Weekly visits for 8 weeks
Duration - 6 months after treatment
Participants are assessed for outcomes including body mass index, physical activity, body image, quality of life, and symptoms up to 6 months after the adapted physical activity program ends.
1 visit at 6 months post-treatment
Trial Site Locations
Total: 7 locations
1
CHU Lille
Lille, France, 59000
Withdrawn
2
Clinique Saint Vincent de Paul
Lyon, France, 69000
Actively Recruiting
3
CHU Montpellier
Montpellier, France, 34000
Actively Recruiting
4
CHU Nantes - service d'addictologie et Psychiatrie de Liaison
Nantes, France, 44000
Actively Recruiting
5
GHU Saine Anne
Paris, France, 75014
Actively Recruiting
6
UDJ Michel Ange
Paris, France, 75016
Actively Recruiting
7
CHU St Etienne
Saint-Etienne, France, 42000
Actively Recruiting
Research Team
N
Nathalie Godart, PU-PH
L
Laurence Kern, MCU
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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