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A Study on the Clinical Efficacy and Preliminary Neural Mechanisms of Repetitive Transcranial Magnetic Stimulation in Addictive Non-Suicidal Self-Injury

A Study on the Clinical Efficacy and Preliminary Neural Mechanisms of Repetitive Transcranial Magnetic Stimulation in Addictive Non-Suicidal Self-Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118744
Enrollment
Unknown
Registered
2026-02-10
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Non-suicidal self-injury with addictive features

Interventions

Sponsors

Huzhou Third Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 23 Years

Inclusion criteria

Inclusion criteria: 1.Meet the DSM-5 diagnostic criteria for Non-Suicidal Self-Injury (NSSI): having engaged in NSSI behavior on at least five occasions in the past 12 months, with at least one episode occurring in the past month; 2.Exhibiting addictive features of NSSI (as indicated by scoring > 2 on >= 3 items of the Ottawa Self-Injury Inventory addiction subscale); 3.Aged 13 to 23 years, with no gender restrictions; 4.Currently not using any psychotropic medications or having received a stable psychopharmacological treatment regimen, and agreeing to continue maintaining the original regimen during the study period; 5.Right-handed; 6.The subject signs the informed consent form; if the subject is under 18 years old, the informed consent form shall be signed by their legal guardian.

Exclusion criteria

Exclusion criteria: 1.Having diagnoses such as bipolar disorder, schizophrenia or other psychotic disorders, obsessive-compulsive disorder, attention-deficit/hyperactivity disorder, autism spectrum disorder or other neurodevelopmental disorders, or borderline personality disorder; 2.Individuals with a cardiac pacemaker or cochlear implant; 3.History of head trauma or seizure; 4.Have undergone modified electroconvulsive therapy, transcranial electrical stimulation, or transcranial magnetic stimulation within the past 3 months prior to enrollment; 5.Individuals with severe physical illnesses, alcohol or substance dependence, intellectual disability, or those unable to complete the required assessments. 6.Pregnant or breastfeeding women; 7.Individuals with severe suicidal ideation or behaviors.

Design outcomes

Primary

MeasureTime frame
Non-Suicidal Self-Injury (NSSI);

Secondary

MeasureTime frame
Hamilton Depression Rating Scale (HAMD) Score;Hamilton Anxiety Rating Scale (HAMA)Score;Barratt Impulsiveness Scale (BIS)Score;

Countries

China

Contacts

Public ContactJin Haiying

Huzhou Third Municipal Hospital

1034167543@qq.com+86 572 2290542

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026