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Development and Preliminary Application Research of a Comprehensive Assessment and Intervention System for Adolescent Depression Based on Virtual Reality Technology

Development and Preliminary Application Research of a Comprehensive Assessment and Intervention System for Adolescent Depression Based on Virtual Reality Technology

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097234
Enrollment
Unknown
Registered
2025-02-14
Start date
2024-03-30
Completion date
Unknown
Last updated
2025-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depressive Episode, Recurrent Depressive Disorder, Depressive State

Interventions

Experimental group:Implementing VR psychological intervention + conventional treatment. Administer VR training intervention to patients in the experimental group for 15 minutes each day, consecutively
Control group:Implementing conventional treatment: including basic medication therapy, psychological therapy, rehabilitation therapy, and physical therapy for adolescent depression patients. Basic med

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Patients meeting the diagnostic criteria for depressive episodes, recurrent depressive disorder, and depressive states according to ICD-10, across various severity levels, were included. (2) Ages between 12 and 18 years old. (3) Voluntary participation in this study and signing of informed consent forms.

Exclusion criteria

Exclusion criteria: (1) Patients with comorbid schizophrenia, organic mental disorders, or any other psychiatric disorders were excluded. (2) Patients with prominent psychotic symptoms such as hallucinations and delusions were excluded. (3) Patients with severe physical illnesses were excluded. (4) Patients with substance dependence, including alcohol dependence, were excluded. (5) Patients who were not suitable for VR devices were excluded. (6) Patients with severe visual impairment, visual field defects, color blindness, and visual neglect were excluded.

Design outcomes

Primary

MeasureTime frame
Self-Rating Depression Scale;

Secondary

MeasureTime frame
Montreal Cognitive Assessment;Somatic Self-rating Scale;The Positive and Negative Affect Scale;(Insomnia Severity Index;

Countries

China

Contacts

Public ContactXiao Qingqing

West China Hospital, Sichuan University

xiaoqingqing66@wchscu.cn+86 138 8010 9576

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026