Bilateral Repetitive Transcranial Magnetic Stimulation for Emotion Regulation in Adolescents with Non-Suicidal Self-Injury: A Randomized Controlled Exploratory Clinical Trial

Authors
Category Primary study
Registry of TrialsChinese Clinical Trial Register
Year 2026
INTERVENTION: Active rTMS + Medication Group :Received rTMS combined with routine pharmacotherapy. rTMS was delivered using a sequential bilateral DLPFC protocol: high frequency stimulation over the left DLPFC (10 Hz, 600 pulses) followed by low?frequency stimulation over the right DLPFC (1 Hz, 1200 pulses), with a total of 1800 pulses per session.;Sham rTMS + Medication Group:Received sham rTMS combined with routine pharmacotherapy. The procedure, coil placement, treatment duration and frequency were identical to the active rTMS group, but a placebo coil was used without effective magnetic field output.;Medication Only Group:Received no rTMS intervention, only standardized pharmacotherapy and routine clinical follow?up.; CONDITION: Adolescent emotional disorders with non‐suicidal self‐injury PRIMARY OUTCOME: Difficulties in Emotion Regulation Scale‐16‐item version, DERS‐16;Columbia‐Suicide Severity Rating Scale (C‐SSRS) ‐ Self‐Injury Items; SECONDARY OUTCOME: Barratt Impulsiveness Scale‐11‐item version, BIS‐11;Hamilton Anxiety Rating Scale‐17‐item version, HAMA‐17;Hamilton Depression Rating Scale‐24‐item version, HAMD‐24;Event‐related potential data; INCLUSION CRITERIA: 1. Aged 12–18 years, with no gender restriction; 2. Meet the diagnostic criteria for Non‐Suicidal Self‐Injury (NSSI) in the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM‐5), with at least one definite NSSI episode in the past 3 months without suicidal intent; 3. Total score of the Difficulties in Emotion Regulation Scale (DERS) is higher than the cutoff value of the Chinese adolescent norm, indicating significant emotion regulation difficulties; 4. Medication status: ‐ For participants already taking psychotropic medications before enrollment, a stable dosage for >=4 weeks is required, with no changes in medication type or dosage during the study to avoid confounding effects on outcomes; ‐ For medication‐naïve participants, routine pharmacotherapy will be initiated by clinicians according to the Chinese Guidelines for the Prevention and Treatment of Depressive Disorders (2025 Edition), with Selective Serotonin Reuptake Inhibi
Epistemonikos ID: 5e71fee63bcd7f9f5095dc980fb3a30c0e57ccb2
First added on: May 09, 2026