Clinical Trials in Spain / NCT07834606
Recruiting Not applicable

Virtual Reality (VR-GINSO) as an Complement to Intervention for Alcohol and Cannabis Use in Youth in Residential Care

NCT07834606 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2025-12-10
Last updated
2026-09-22

Condition(s) studied

Dual DiagnosisRisk YouthAntisocial Behavior

Investigational drug(s) / intervention(s)

Virtual RealityTreatment as Usual (TAU)

Virtual Reality: This group will undergo a 1 individual session with a Virtual Reality program targeting emotion recognition, training on avoidance-approximation to associated stimuli, and exposure to conditioned contexts for substance use. During this session, participants will train specific abilities throug various activities. The tasks have been designed as a serious game in a Virtual Reality setting and include: emotion identification and recognition, practicing avoidance of conditioned substance use stimuli, and approximation to neutral stimuli, and exposure to conditioned situations to train regulation and management abilities for craving.

Treatment as Usual (TAU): Participants in this group will receive treatment as usual provided by the facility, with no additional intervention. Treatment will be delivered ober the same period of time as in the other study group. Participants will complete one baseline assessment before the study period, and one post-intervention assessment.

Study summary

The goal of this RCT is to evaluate the effects of a virtual reality intervention on self-efficacy regarding alcohol and cannabis use among at-risk youth in various residential mental health treatment centers who have co-occurring disorders and are under the care of the association where they receive treatment. The main question it aims to answer is:

• Does the VR intervention enhance the therapeutic effect of residential treatment on self-efficacy regarding alcohol and cannabis use? If there is a comparison group: Researchers will compare the intervention with the usual care (UC) that minors receive at the centers for the treatment of dual diagnosis to see if VR adds value to this treatment.

Participants will be randomly assigned to each condition and will be evaluated before and after one month. In the experimental group, participants will receive a treatment session using VR software, during which they will undergo training in the following modules: The first phase is an assessment phase, during which objective measures are determined for 1) emotional recognition, 2) avoidance/approach toward related stimuli, 3) degree of compliance with social pressure, and 4) craving in the presence of the drug, exposure to cues, and/or conditioned contexts.

Eligibility

Sex
ALL
Min age
13 Years
Max age
21 Years
Healthy volunteers
No
Inclusion Criteria: * 13-21 years old * Admited in a residencial intervention program * Prevision of a \>6 month stay * Alcohol and/or cannabis use Exclusion Criteria: * Psychiatric or neurological pahology that affects cognitive functions * Not being fluent in Spanish

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Universidad Francisco de Vitoria Pozuelo de Alarcón Madrid Recruiting

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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 NCT07834606 on ClinicalTrials.gov ↗ ← All trials in Spain