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Clinical study of accelerated cTBS intervention for adolescent depression with non-suicidal self-injurious behavior

Clinical study of accelerated cTBS intervention for adolescent depression with non-suicidal self-injurious behavior

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067908
Enrollment
Unknown
Registered
2023-01-31
Start date
2023-02-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Depression

Interventions

cTBS group:10-day real cTBS intervention with 5 times per day targeted at right DLPFC
sham cTBS group:10-day sham cTBS intervention with 5 times per day targeted at right DLPFC

Sponsors

Ningbo Kangning Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Diagnosed with depression Five or more days of self-injury within a year, but no suicidal ideation or attempt; 12-18 years of age; No organic disease such as encephalitis, meningitis, or traumatic brain injury; No major psychiatric illnesses such as major depression, schizophrenia, dysthymia, etc; No contraindications to EEG (scalp trauma, inability to sit still).

Exclusion criteria

Exclusion criteria: Patients with severe somatic, infectious and immune system disorders Patients with severe neurological disorders, mental retardation or organic brain disease; those who have received electroconvulsive therapy within the last 3 months with a history of previous seizures. Those assessed as unsuitable for cTBS treatment and those who are unable to complete the relevant index collection.

Design outcomes

Primary

MeasureTime frame
Ottawa Self-Injury Scale;Depression Inventory;Anxiety Inventory;EGI EEG measurements;

Secondary

MeasureTime frame
Neurocognitive measures;

Countries

China

Contacts

Public ContactXiaoli Liu

Ningbo Kangning Hospital

1206207800@qq.com+86 18268694753

Outcome results

None listed

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