Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06434766

Multicenter iTBS Neuromodulation for PTSD Treatment

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2026-04-24

140

Participants Needed

5

Research Sites

134 weeks

Total Duration

On this page

Sponsors

S

Second Affiliated Hospital, School of Medicine, Zhejiang University

Lead Sponsor

S

Shanghai Mental Health Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

The proposed study aims to evaluate the efficacy of intermittent theta-burst transcranial magnetic stimulation (iTBS) targeting primary motor cortex (M1) as adjunct treatment for PTSD patients. The primary outcome measure includes changes in PTSD symptom severity, with secondary outcome measures focusing on negative moods improvements, quality of life and social/occupation functioning and functional connectivity of the brain.

CONDITIONS

Official Title

Multicenter iTBS Neuromodulation for PTSD Treatment

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged between 18 to 65 years old
  • Right handedness
  • Have a diagnosis of PTSD meeting DSM-5 criteria
  • CAPS-5 score >35
  • Under stable medication for at least four weeks
  • Capable of independently reading and understanding study materials and providing informed consent.
Not Eligible

You will not qualify if you...

  • Current or past significant neurological or medical disorder including seizure disorder, CNS tumors, stroke, or cerebral aneurysm
  • Primary psychotic disorder, bipolar I disorder, major depressive disorder, or personality disorders
  • Lifetime history of attempted suicide or high suicide risk based on HAMD-17 item
  • Implanted brain device or metal implants, pacemaker, extensive dental work, or magnetic metal implants and upper body tattoos if undergoing fMRI
  • Previous experience with repetitive transcranial magnetic stimulation (rTMS)
  • Pregnancy, lactation, or planning pregnancy during the study
  • Currently receiving psychological or other physical treatments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Shanghai Mental Health Center

Shanghai, Shanghai Municipality, China

Actively Recruiting

2

First Affiliated Hospital of Anhui Medical University

Hangzhou, Zhejiang, China

Actively Recruiting

3

Second Affiliated Hospital Zhejiang University School of Medicine

Hangzhou, Zhejiang, China

Actively Recruiting

4

The Affiliated Kangning Hospital of Ningbo University

Ningbo, Zhejiang, China

Actively Recruiting

5

Tongji Hospital of Tongji University

Shanghai, China

Actively Recruiting

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Research Team

H

Huiqian Huang, Ph.D.

CONTACT

S

Shanshan Li, Bachelor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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