Body Image Disorder in Anorexia Nervosa and Virtual Reality
NCT ID: NCT03118921
Last Updated: 2021-12-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
17 participants
INTERVENTIONAL
2017-04-20
2019-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DEVICE_FEASIBILITY
NONE
Study Groups
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Virtual reality
The first session aims to present the virtual reality material that will be used. The second session will take place 2 weeks after the first session and will consist of the use of the immersion software
Virtual reality
The first session aims to present the virtual reality material that will be used. The second session will take place 2 weeks after the first session and will consist of the use of the immersion software.
Interventions
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Virtual reality
The first session aims to present the virtual reality material that will be used. The second session will take place 2 weeks after the first session and will consist of the use of the immersion software.
Eligibility Criteria
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Inclusion Criteria
* Post-puberty
* Pure restrictive anorexia nervosa, diagnosis by the DSM-V
* BMI \<17.5
* Patient attending an outpatient clinic at the Bohars Psychiatric Hospital in France
* Having signed the Informed Consent Form
* For minor patients, signing the form of informed consent of both parents
Exclusion Criteria
* Psychiatric disorders (characterized depressed, anxiety disorder)
* Neurological Disorders
* Mental retardation
* Abuse or addiction to alcohol
* Abuse or dependence on psychoactive substances in the previous year.
* Patient with a protective justice measure
16 Years
40 Years
FEMALE
No
Sponsors
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University Hospital, Brest
OTHER
Responsible Party
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Locations
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CHRU Brest
Brest, , France
Countries
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Other Identifiers
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REVAM
Identifier Type: -
Identifier Source: org_study_id