Anorexia Nervosa Clinical Trial
— ANO-TERVOfficial title:
Efficiency of Virtual Reality Exposure Therapy in the Management of Body Dysmorphic Disorder in Female Adolescents With Anorexia Nervosa: a Randomized, Controlled Superiority Study
Verified date | March 2023 |
Source | CHU de Reims |
Contact | Julien EUTROPE |
Phone | 03 26 78 39 56 |
jeutrope[@]chu-reims.fr | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Anorexia nervosa is defined in DSM V as a quantitative and qualitative dietary restriction resulting in significant weight loss, intense fear of weight gain, altered weight and body shape perception (body dysmorphic disorder) and low self-esteem influenced by weight or body shape. Body dysmorphic disorder is the most difficult symptom to manage in anorexia nervosa and its persistence is a factor associated with relapse. Virtual reality exposure therapy has proven its effectiveness in the management of post-traumatic stress disorder in the military and is a widely used therapy. The effectiveness of this treatment using new technologies has not yet been studied for the treatment of body dysmorphic disorder in anorexia nervosa and is not used routinely. It could represent an interesting alternative to the physical approach in psychomotor therapy, traditionally offered to patients suffering from anorexia nervosa. It is important to evaluate the effectiveness of virtual reality exposure therapy in the management of body dysmorphic disorder in patients with anorexia nervosa by comparing these two care techniques.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | September 20, 2028 |
Est. primary completion date | March 20, 2027 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 13 Years to 17 Years |
Eligibility | Inclusion criteria : - Female adolescents aged 13 to 18 - with a diagnosis of anorexia nervosa of all types (including purgative and hyperphagic) according to the DSM-V - French as first language - agreed to participate in the study - parental authority holders accepting her participation in the study - affiliated to a social security system Patients will not be included in the study: - with a somatic severity criterion: - Total aphagia - Body mass index (BMI) < 14kg/m² for those over 17 years of age, BMI < 13.2kg/m² for those aged 15-16 and BMI < 12.7kg/m² for those aged 13-14. - Confusion - Bradycardia <40/min, Tachycardia - Blood pressure < 80/50mmHg - Hypothermia <35.5°C - Severe metabolic disorders: hypokalemia < 2.5 mmol/l, hyponatremia < 125mmol/l or hypernatremia > 150 mmol/l, hypophosphoremia < 0.5 mmol/l - Acetonuria, hypoglycemia < 0.6g/l - Creatinine elevation > 100micromol/l - Cytolysis > 4N - Leuconeutropenia <1000/mm3 - Thrombocytopenia <6000000/mm3 - Suicide attempt in the last month before inclusion - Receiving benzodiazepine treatment outside the prescription limits. - Psychotic patients or patients with psychoactive substance addiction according to MINI KID criteria (Sheehan DV et al. Reliability and validity of the Mini International Neuropsychiatric Interview for children and adolescents (MINI Kid). J Clin Psychiatry 2010;71(3):313-326). |
Country | Name | City | State |
---|---|---|---|
France | Damien JOLLY | Reims |
Lead Sponsor | Collaborator |
---|---|
CHU de Reims |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Body Shape Questionnaire | The Body Shape Questionnaire (BSQ) measures concerns about body shape. The BSQ can be divided into 4 sub scores: "avoidance and social shame of body exposure", "body dissatisfaction with lower body parts", "use of laxatives and vomiting to reduce body dissatisfaction" and "inappropriate cognitions and behaviours to control weight". | 12 months | |
Secondary | Eating Disorder Inventory | Eating Disorder Inventory (EDI-2) is a self questionnaire to assess the severity of symptoms of eating disorders and to evaluate their changes | 12 months |
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