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| Name | Class |
|---|---|
| AGIR à Dom | OTHER |
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The goal of this pilot clinical trial is to assess a program of Home-based Adapted Physical Activity in Anorexia Nervosa.
The main questions it aims to answer are: Determining the acceptability of this program / Determining the feasibility and safety of this program / Determining patient satisfaction / Measuring the evolution of the symptomatology. Participants will follow a program of Home-based Adapted Physical Activity.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Home-based Adapted Physical Activity | Experimental | Home-based Adapted Physical Activity sessions by videoconference |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Home-based Adapted Physical Activity | Behavioral | There will be 8 weekly sessions at a time defined in advance for the same group and for the 8 sessions |
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| Measure | Description | Time Frame |
|---|---|---|
| Acceptability of a telerehabilitation adapted physical activity (APA) program for patient with anorexia nervosa quantitatively | Number of patients who have realized the first of the 8 adapted physical activity session in relation to the total number of eligibly patients who have been invited to participate at the study | at the first session of the APA program (Day 0) |
| Acceptability of a telerehabilitation adapted physical activity program for patient with anorexia nervosa qualitively | Reasons for refusal and participation's age will be collected anonymously for patients who refuse inclusion but agree to this informations being collected | at the first session of the APA program (Day 0) |
| Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively | Number and portion of patients who have realized the 8 adapted physical activity sessions as well as the first and final sessions | at the end-of-study visit (Day 0 + 11 weeks) |
| Feasibility and safety of a telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively | Motifs of no realization of one ou more sessions will be collected. They will inclued technical problems, personal, professional ou medical constraints inclued study's exit for weight loss | at the end-of-study visit (Day 0 + 11 weeks) |
| Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa quantitatively | Portion of patients answing "yes" at the question : "Would you like to continue this program ?" | at the final session of APA programm (Day 0 + 8 weeks) |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cécile BETRY | Grenoble | France | ||||
| Pr GUILLAUME Sébastien |
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| ID | Term |
|---|---|
| D000856 | Anorexia Nervosa |
| ID | Term |
|---|---|
| D001068 | Feeding and Eating Disorders |
| D001523 | Mental Disorders |
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| Patient satisfaction with the telerehabilitation adapted physical activity program for patients with anorexia nervosa qualitively | Programm's motifs of satisfaction or no satisfaction will be collected during the final session of adapted physical activity program | at the final session of APA programm (Day 0 + 8 weeks) |
| Measuring changes in symptomatology in key areas such as self-esteem through self-assessment questionnaire | Determination of this parameter :self-esteem by self-esteem scale of Rosenberg | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Measuring changes in symptomatology in key areas such as quality of life through self-assessment questionnaire | Determination of this parametes :quality of life by QUAVIAM scale | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Measuring changes in symptomatology in key areas such as dependence on physical activity through self-assessment questionnaire | Determination of this parameter : dependence on physical activity by EDQ questionnary | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Measuring changes in symptomatology in key areas such as dependence on physical activity through objective measure | Determination of this parameter : level of physical activity by 7-day actimetry recording | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Measuring changes in symptomatology in key areas such as changes in weight through objective measure | Determination of this parameter : weight in kilograms on a classic scale | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Measuring changes in symptomatology in key areas such as body composition through objective measure | Determination of this parameters : the body composition will be determinated by a impedancemetry measurement | at the early study visit (Day 0 - 4 weeks) and at end-of-study visit (Day 0 + 11 weeks ) |
| Montpellier |
| France |