Actively Recruiting

Phase Not Applicable
Age: 0 - 60Years
All Genders
NCT06642675

nTMS for Negative Symptom in Schizophrenia

Led by Central South University · Updated on 2025-12-05

40

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to test the effectiveness of Navigated transcranial magnetic stimulation (nTMS) of left Supramarginal Gyrus for negative symptoms. In this double-blind, randomized controlled trial, patients will be assigned to active iTBS experimental group or sham iTBS group. Treatment will last for 10 days, and data will be collected at baseline, 1 day and 1 month after treatment.

CONDITIONS

Official Title

nTMS for Negative Symptom in Schizophrenia

Who Can Participate

Age: 0 - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of schizophrenia according to ICD-11
  • Diagnosis confirmed with SCID-5-RV (DSM-5 Structured Clinical Interview)
  • Score more than 4 points on any negative symptom item (N1-N7)
  • Age less than 60 years
Not Eligible

You will not qualify if you...

  • Diagnosis of neurodevelopmental disorders, bipolar disorder, or substance use disorders (except alcohol and tobacco)
  • Severe or acute physical illnesses such as traumatic brain injury, brain infections, cardiovascular or respiratory diseases, hematological disorders
  • Genetic diseases like tuberous sclerosis, multiple sclerosis, Kleefstra syndrome, 22q11.2 deletion syndrome, Prader-Willi syndrome, Klinefelter syndrome
  • Contraindications for MRI or rTMS including metal implants, epilepsy, cochlear implants
  • Severe risk of self-injury or suicide
  • Other conditions judged unsuitable for treatment by researchers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mental Health Institute of Second Xiangya Hospital,CSU

Changsha, Hunan, China, 410011

Actively Recruiting

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Research Team

R

Renrong Wu, M.D., Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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