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Exploring the changes in brain function in adolescent with depressive during competitive and cooperative tasks based on functional near-infrared spectroscopy hyperscanning and functional connectivity.

Exploring the changes in brain function in adolescent with depressive during competitive and cooperative tasks based on functional near-infrared spectroscopy hyperscanning and functional connectivity.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400081712
Enrollment
Unknown
Registered
2024-03-10
Start date
2024-03-10
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Depression

Interventions

Depression group:None
Healthy control group:None

Sponsors

the Affiliated Hospital of GuiZhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 17 Years

Inclusion criteria

Inclusion criteria: Healthy control group: ? Age: 13-17 years old; ? HAMD-2420 points, diagnosed by two psychiatrists at or above the level of attending physician, meets the diagnostic criteria for "depressive episodes" in the Diagnostic and Statistical Manual of Mental Disorder Five (DSM-V) of the United States; ? Not taking antidepressants, anesthetics, or sleeping pills for the first time or in the past 3 months; ? No other organic disease patients or other serious or uncontrolled stable physical diseases; ? Voluntarily participate in the experiment, understand the research content, and sign an informed consent form; ? The inclusion criteria for the accompanying father/mother participating in the experiment are the same as those of the normal group.

Exclusion criteria

Exclusion criteria: Depression group: ? those with other mental disorders, such as schizophrenia, mental retardation, or severe organic diseases; ? Substance abuse and dependence; ? Those who exhibit obvious impulsive behavior and are unable to cooperate with the examination. Healthy control group: ? Individuals who have previously suffered from mental illnesses such as schizophrenia, depressive episodes, bipolar disorder, mental retardation, or severe organic diseases in DSM-5; ? Substance abuse and dependence; ? Those who exhibit obvious impulsive behavior and are unable to cooperate with the examination.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale,HAMD;

Secondary

MeasureTime frame
Family adaptability cohesion scale ?-Chinese version,FACES?- CV;

Countries

China

Contacts

Public ContactYiMing Wang

the Affiliated Hospital of GuiZhou Medical University

Yimingw66@yahoo.com+86 135 1196 7666

Outcome results

None listed

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