Ireland
--:--IST
Recruiting Not applicable

Improving the Treatment of Anorexia Nervosa in Children Through Virtual Reality Body Exposure

NCT06166355 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2024-07-01
Last updated
2026-05-08

Condition(s) studied

Anorexia Nervosa

Investigational drug(s) / intervention(s)

Attentional Bias Modification TrainingVR-based body exposureCognitive-behavioral therapy

Attentional Bias Modification Training: Combine usual cognitive-behavioral treatment (CBT) sessions with additional five VR-based body-exposure therapy sessions and five sessions of Attentional Bias Modification Training.

VR-based body exposure: Combine usual cognitive-behavioral treatment (CBT) sessions with additional five VR-based body-exposure therapy sessions

Cognitive-behavioral therapy: Usual cognitive-behavioral treatment (CBT) sessions.

Study summary

The age of onset of anorexia nervosa has been progressively decreasing in recent years. Also, the prevalence rates of childhood anorexia in many countries have grown significantly. This increase was already observed before the COVID-19 pandemic, but the confinements and the stress derived from them have caused this increase to accelerate. As in adolescent and adult patients, in childhood anorexia some of the core signs and symptoms are an extreme fear of gaining weight and avoidance of food. The consequences of the early-onset of anorexia can be very important since the maturation of the organism is more incomplete in children than in adolescents. Weight loss can have very severe consequences, since in children the percentage of body fat is lower. On the other hand, hormonal disorders derived from food deprivation also have very severe consequences for the development of different organs. General physical development and growth can be affected, with consequences such as not being able to reach normal height. The research carried out to date on the efficacy of treatments for childhood anorexia is very scarce. There are no specific treatment strategies or settings for children with anorexia, and little research has been done to tailor treatment for younger patients. Given the need to explore new treatments for anorexia nervosa specifically aimed at children, the objective of this project is to develop a program to carry out exposure to one's own body through virtual reality, gradually, with progressive increases in size until achieving a healthy weight. In the virtual exposure, patients will observe the image of an avatar in a mirror for the time necessary in each session to produce the reduction of the anxiety response. The avatars that will be developed for this purpose will have a physical constitution corresponding to children under 14 years of age, and physical proportions equivalent to those of each patient. The positive results obtained with a previous version of this treatment originally developed for adolescents and adults suggest that its adaptation to children can open new ways for exploring effective treatments for childhood anorexia.

Eligibility

Sex
ALL
Min age
—
Max age
14 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with a primary diagnosis of anorexia nervosa (DSM-V) * Patients below 14 years old * Patients with BMI \<18.5 * Subsyndromal patients will also be included Exclusion Criteria: * Visual deficits * Epilepsy or neuroleptic medication * Psychotic disorder * Bipolar disorder * Medical complications * Pregnancy * Clinical cardiac arrhythmia

Primary outcome measure(s)

  • Change in Eating Disorder symptomatology: Eating Disorders Inventory-3 (EDI-3; Garner, 2004) drive for thinness (EDI-DT) scale — From pre-assessment to post-assessment after 6 weeks , and at the six-month follow-up
    Evaluation of the change in drive for thinness, with maximum possible score of 28, where higher scores indicate higher drive for thinness.
  • Change in Eating Disorder symptomatology: Eating Disorders Inventory-3 (EDI-3; Garner, 2004) body dissatisfaction (EDI-BD) scale — From pre-assessment to post-assessment after 6 weeks , and at the six-month follow-up
    Evaluation of the change in body dissatisfaction, with maximum possible score of 40, where higher scores indicate higher body dissatisfaction.
  • Change in body mass index values — From pre-assessment to post-assessment after 6 weeks , and at the six-month follow-up
    Evaluation of change in Body Mass Index values

Trial sites (1)

FacilityCityRegionStatus
Hospital Sant Joan de Déu Barcelona Barcelona Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06166355 on ClinicalTrials.gov ↗ ← All trials in Spain