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Accelerated iTBS intervention in adolescent depression

Clinical study of accelerated iTBS intervention in adolescent depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083002
Enrollment
Unknown
Registered
2024-04-12
Start date
2024-05-18
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Adolescent depression

Interventions

iTBS group:real stimulation

Sponsors

Ningbo Kangning Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for depression as defined by ICD-10; 2. Has no trauma or other brain disorders, and no metal implants in the body; 3. Clearly understands and voluntarily participates in this study, and signs the informed consent form; 4. Right-handed

Exclusion criteria

Exclusion criteria: 1. Patients with severe physical, infectious and immune disorders 2. Patients with severe neurological disorders, mental retardation or organic brain disorders 3. Pregnant or breastfeeding women 4. Patients who have received electroconvulsive therapy in the last 3 months 5. Patients with a history of epileptic seizures 6. Patients who are assessed to be unsuitable for iTBS and who are not able to complete the collection of relevant indicators.

Design outcomes

Primary

MeasureTime frame
Depression scale;

Secondary

MeasureTime frame
Neuropsychometric measures related to cognitive behaviour;Anxiety symptom, suicidal ideation;Electrophysiological indicators;

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