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Repeat Transcranial magnetic stimulation for adolescent depression with non-suicidal Non-suicidal self-injury

Repeat Transcranial magnetic stimulation for adolescent depression with non-suicidal Non-suicidal self-injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109892
Enrollment
Unknown
Registered
2025-09-26
Start date
2023-02-03
Completion date
Unknown
Last updated
2025-09-29

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

Conditions

depression

Interventions

Experimental group :Patients were treated with three iTBS treatments per day (1800 pulses, 50 minutes apart, stimulation intensity determined according to the patients tolerance, but not more than 120
Control group:Participants maintained a stable antidepressant medication regimen during the trial.

Sponsors

The Third People's Hospital of Yunnan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 19 Years

Inclusion criteria

Inclusion criteria: 1. Patients who met the diagnostic criteria of Diagnostic and Statistical Manual of Mental Disorders (5 th) (DSM-5) for both depressive episodes and non-suicidal self-injurious; 2. Age 13-19 years; 3. Baseline Hamilton Depression Scale-17 scores are >=17; 4. Patients and his/her parent voluntarily participated in the study, understood and signed a written informed consent; 5.Participants maintained a stable antidepressant medication regimen during the trial.

Exclusion criteria

Exclusion criteria: 1. Patients with previous mental retardation, schizophrenia, compulsive disorder, bipolar disorder, or any other mental disorder are excluded; 2. depressive episodes secondary to other mental or physical disorders; 3. severe or unstable cardiac, liver, kidney, endocrine(thyroid diseases), blood, autoimmune diseases; 4. Women during lactation, pregnancy, or may become pregnant during the trial; 5. Previous or current alcohol dependence, significant substance abuse / dependence; 6. Those who have previously failed TMS, did not respond to ECT, or have a history of systemic psychotherapy; 7. Those who currently have contraindications to TMS, such as epilepsy or other organic brain sexual disease patients, newly implanted heart stents, metal dentures, etc.

Design outcomes

Primary

MeasureTime frame
Chinese Revised Ottawa Self-Injury Scale;17-item Hamilton Depression Scale;

Secondary

MeasureTime frame
Hamilton anxiety scale;

Countries

China

Contacts

Public ContactJiang Lizhu / Cao Fang

The Third People's Hospital of Yunnan Province

1824056729@qq.com+86 184 6913 3202

Outcome results

None listed

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