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Repetitive Transcranial Magnetic Stimulation for Negative Symptoms of Chronic Schizophrenia: Efficacy, Neural Mechanisms and a Double-Blind Sham-Controlled Randomized Trial

Repetitive Transcranial Magnetic Stimulation for Negative Symptoms of Chronic Schizophrenia: Efficacy, Neural Mechanisms and a Double-Blind Sham-Controlled Randomized Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127131
Enrollment
Unknown
Registered
2026-06-25
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Chronic Schizophrenia

Interventions

Sham stimulation group:sham repetitive transcranial magnetic stimulation (rTMS) therapy
Active stimulation group:repetitive transcranial magnetic stimulation (rTMS)

Sponsors

The Third Hospital of Jinjiang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Met the diagnostic criteria for schizophrenia specified in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). 2. Disease duration of no less than 2 years with stable clinical condition and no acute exacerbations in the preceding 3 months. 3. A score of >= 20 on the PANSS Negative Subscale. 4. Aged 18 to 65 years. 5. Able to cooperate with scale assessments, electroencephalography examinations and rTMS treatment. 6. Voluntary participation with written informed consent obtained from both patients and their family members.

Exclusion criteria

Exclusion criteria: 1. Presence of severe physical illnesses (e.g., cardiovascular and cerebrovascular diseases, liver or renal failure) or neurological disorders. 2. Intellectual disability or severe hearing/visual impairment. 3. Severe impulsive or violent behaviors that interfere with treatment cooperation. 4. Alcohol or psychoactive substance dependence. 5. Absolute contraindications to rTMS: intracranial or implanted metallic devices (e.g., aneurysm clips, cochlear implants, deep brain stimulators); cardiac pacemakers; personal or first-degree family history of epilepsy; confirmed or suspected pregnancy; severe craniocerebral trauma or prior intracranial surgery. 6. Received rTMS treatment within the past 6 months. 7. Worsening clinical condition requiring medication adjustment or transfer to the acute ward during the intervention period. Such cases were recorded as dropouts but retained in the intention-to-treat (ITT) analysis.

Design outcomes

Primary

MeasureTime frame
Positive and Negative Syndrome Scale (PANSS);

Secondary

MeasureTime frame
Clinical Global Impression-Severity (CGI-S);Safety indicators: Recording of adverse events;17-item Hamilton Anxiety Rating Scale (HAMA-17);Social Disability Screening Schedule (SDSS);Electroencephalographic event-related potential data (MMN and P300);Clinical Global Impression-Improvement (CGI-I);Intrinsic Motivation Inventory-Short Revised (IMI-SR);24-item Hamilton Depression Rating Scale (HAMD-24);

Countries

China

Contacts

Public ContactJiaren Zheng

The Third Hospital of Jinjiang

150482573@qq.com+86 595 8677 7273

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026