Informations générales (source: ClinicalTrials.gov)
Impact of an Adapted Physical Activity Program Supervised by Videoconference in Patients With Anorexia Nervosa: a Pilot Study (APAREXIM-P)
Interventional
N/A
University Hospital, Caen (Voir sur ClinicalTrials)
novembre 2022
décembre 2026
29 juin 2024
The primary objectives of the APAREXIM'Pilot study are to evaluate the short- and
medium-term effects of a live supervised Adapted Physical Activity (APA) program via
videoconferencing on:
- Feasibility and acceptability of APA via videoconferencing by the patients.
- The primary symptoms of Anorexia Nervosa (AN).
The secondary objectives are to evaluate the impact of this program on :
- Mental health
- Physical condition
- Sleep-wake cycle (sleep disturbance and physical hyperactivity)
The patients will first undergo an inclusion visit (T0) at the University Hospital of
Caen, then a first evaluation session (T1) at the COMETE laboratory in Caen (physical
tests, questionnaires, sleep diary, actimetry). They will then be randomly divided into 2
groups: 15 patients who will follow an APA program supervised by videoconference for 8
weeks (AM-APA) at their home, in addition to the usual outpatient treatment, and 15
patients who will benefit only from the classic outpatient treatment (AM-T). All patients
will undergo two additional evaluation sessions at one week post-program (T2) and at 3
months post-program (T3).
Etablissements
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
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Caen University Hospital - 14033 - Caen - Calvados - France | Contact (sur clinicalTrials) |
Critères
Femme
Inclusion Criteria:
- Female patient between 13 and 18 years old, with typical anorexia nervosa symptoms
diagnosed by a specialist.
- Patient followed in outpatient care.
- Collection of the signature of the informed consent.
- Patient affiliated to the health insurance system.
- Agreement of the legal representatives
- Female patient between 13 and 18 years old, with typical anorexia nervosa symptoms
diagnosed by a specialist.
- Patient followed in outpatient care.
- Collection of the signature of the informed consent.
- Patient affiliated to the health insurance system.
- Agreement of the legal representatives
- Patient with contraindications to physical activity or with a state of health judged
critical by the doctor.
- Person deprived of liberty by judicial or administrative decision, or under
guardianship or curatorship.
- Pregnant or breast-feeding woman.
- Patient included in another biomedical research protocol during the present study.