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Research on the Precision Physical Intervention System for Adolescent Emotional Disorders Assisted by Augmented Reality Fusion

Research on the Precision Physical Intervention System for Adolescent Emotional Disorders Assisted by Augmented Reality Fusion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100806
Enrollment
Unknown
Registered
2025-04-15
Start date
2025-04-25
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Emotional Disorder

Interventions

Experimental group:Precision Physical Intervention System for Adolescent Emotional Disorders Assisted by Augmented Reality Fusion
Control group:Augmented Reality Fusion-assisted Precise Physical Intervention System for Adolescent Mood Disorders, Fake Intervention

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 25 Years

Inclusion criteria

Inclusion criteria: a) Center for Epidemiologic Studies Depression Scale (CES-D) >=16 points or Beck ChineseDepression inventory-II-Chinese (BDI-II-C) >=15 points; b) Age 12-25 years; c) The guardian of the subject voluntarily participates in the intervention and is able to cooperate in completing the intervention and signing the informed consent form.

Exclusion criteria

Exclusion criteria: a) According to DSM-IV or DSM-V, diagnosed with symptoms of concurrent mental confusion, meeting other diagnostic criteria for mental disorders, such as anxiety disorder, schizophrenia, schizoaffective disorder, bipolar disorder, etc.; b) Self-harm or suicidal behavior within the past year; c) Contraindications such as metallic foreign bodies or any other electronic devices implanted in the body; d) Have a history of neurological diseases such as epilepsy and traumatic brain injury; e) Have severe visual, auditory or motor impairment and cannot cooperate with the examination and intervention; f) Suffering from severe liver and kidney dysfunction or other serious medical diseases; g) Neuromodulation interventions such as eye movement stimulation, transcranial magnetic stimulation (TMS), and transcranial magnetic resonance image guided focused ultrasound (TcMRgFUS) within 3 months prior to enrollment; h) Those who are participating in other clinical research trials.

Design outcomes

Primary

MeasureTime frame
Time spent on areas of interest;

Countries

China

Contacts

Public ContactShijun Li

Chinese PLA General Hospital

shijunli07@yeah.net+86 10 6693 7564

Outcome results

None listed

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