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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03426930 |
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Date of registration:
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02/02/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Contribution of a Virtual Reality Program in the Treatment of Dysmorphophobia for Adolescent Female With Anorexia Nervosa
TERV-TCA |
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Scientific title:
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Contribution of a Virtual Reality Program in the Treatment of Dysmorphophobia for Adolescent Female With Anorexia Nervosa |
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Date of first enrolment:
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January 17, 2018 |
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Target sample size:
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30 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT03426930 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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France
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Contacts
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Name:
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Flora BAT, PH |
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Address:
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Telephone:
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491745860 |
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Email:
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flora.bat@ap-hm.fr |
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Affiliation:
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Name:
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Flora BAT, PH |
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Address:
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Telephone:
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491745850 |
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Email:
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flora.bat@ap-hm.fr |
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Affiliation:
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Name:
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Jean-Olivier ARNAUD, General Director |
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Address:
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Telephone:
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Email:
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Affiliation:
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ASSISTANCE PUBLIQUE HÔPITAUX DE MARSEILLE |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Age between 13 et 18 years old
- Female subject
- Females with anorexia nervosa according to the diagnostic criteria of DSM-5
- The patient, the parents or the legal representative (s) have given written consent
- Possessing a social security scheme
Exclusion Criteria:
- Male subject
- Age under 13 years or over 18 years
- Subject presenting a contra-indication to virtual reality
- Subject, or parents who refused to sign informed consent
Age minimum:
13 Years
Age maximum:
18 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Anorexia Nervosa
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Intervention(s)
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Other: Cognitive-behavioral psychotherapies
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Other: self-evaluation of the Body Mass Index
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Primary Outcome(s)
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Evaluation of non-self Body Mass Index
[Time Frame: 24 months]
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Eating Disorder Inventory 2 (EDI)
[Time Frame: 24 months]
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Secondary ID(s)
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2017-40
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2017-A02836-47
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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