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The effect of virtual reality-based cognitive training system and eye movement desensitization and reprocessing system in depressed patients

The effect of virtual reality-based cognitive training system and eye movement desensitization and reprocessing system in depressed patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057820
Enrollment
Unknown
Registered
2022-03-18
Start date
2018-07-01
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Depression

Interventions

Cognitive training group (adult):VR-based cognitive training
EMDR group (adult):VR-based EMDR
Cognitive training group (children&adolescent):VR-based cognitive training
Cognitive training&EMDR group (children & adolescent):VR-based cognitive training+VR-based EMDR
Control group(adult):Treatment as usal
Control group(children&adolescent):Treatment as usal
EMDR group(children&adolescent) :VR-based EMDR
CCRT group:CCRT intervention

Sponsors

First Affiliated Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Participants diagnosed as major depressive disorder or bipolar depression according to the Diagnostic and statistical manual of mental disorders, Fifth edition (DSM-5); 2. Aged 10-45 years old; 3. Normal vision and right-handed; 4. Have not received an MCCB or DN-CAS cognitive assessment before enrollment; 5. Volunteer to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Other Axis I psychiatric disorders and symptoms; 2. A history of the use of electroconvulsive therapy; 3. High risk of suicide; 4. A history of neurological or organic brain disorder; 5. A history of alcohol/substance abuse; 6. Any physical illness demonstrated by personal history or clinical or laboratory examinations, pregnancy, or postpartum depression; 7. Virtual reality sickness.

Design outcomes

Primary

MeasureTime frame
Hamilton depression scale,HAMD;Hamilton Anxiety Scale, HAMA;Young Mania Rating Scale ,YMRS;Patient Health Questionnaire-9, PHQ-9;Generalized Anxiety Disorder, GAD-7;Hypomania Check List,HCL-32;Childhood Trauma Questionnaire,CTQ;PTSD CheckList-Civilian Version, PCL-C;Massachusetts General Hospital Cognitive and Physical Functioning Questionnaire,CPFQ;MATRICS Consensus Cognitive Battery,MCCB;Beck Scale for Suicide Ideation,BSSI;Das-Naglieri:Cognitive Assessment System,DN:CAS;Rejection Sensitivity Questionnaire,RSQ;Emotional Intelligence Scale,EIS;Adolescents Self-injury Scale,ASIS;Resilience Scale for Chinese Adolescents,RSCA;Perceived Social Support Scale,PSSS;Fam-ily Assessment Device,FAD;Adolent Self-Rating Life Events Check List,ASLEC;Columbia-Sui-Severity Rating Scale, C-SSRS;NAA/Cr ratios of prefrontal cortex;NAA/Cr ratios of basal ganglia;NAA/Cr ratios of cerebellum;mI/Cr ratios of prefrontal cortex;mI/Cr ratios of basal ganglia;mI/Cr ratios of cerebellum;Cho/Cr ratios of prefrontal cortex;Cho/Cr ratios of basal ganglia;Cho/Cr ratios of cerebellum;

Countries

China

Contacts

Public ContactYanbin Jia

First Affiliated Hospital of Jinan University

jnufyyjsyxk@126.com+86 15521088946

Outcome results

None listed

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