The Efficacy and Safety of Temporal Interference Stimulation in the Treatment of Post-Traumatic Stress Disorder

Recruiting N/A Interventional Study
Post-traumatic Stress Disorder (PTSD)
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 50
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
5 (estimated)
Sponsor
Shanghai Mental Health Center · Other
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About This Trial

This study aims to evaluate the efficacy and safety of Temporal Interference (TI) stimulation in treating patients with post-traumatic stress disorder (PTSD) and to explore its potential neural mechanisms using magnetic resonance imaging (MRI) ,magnetoencephalography(MEG),electroencephalography (EEG).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age 18-50 years, male or female 2. Diagnosis of PTSD per DSM-5 (assessed by CAPS-5), with symptom duration of at least 3 months, and PTSD as the current primary diagnosis; comorbid depressive disorder or anxiety disorder is allowed 3. If currently receiving psychiatric medica…
Contacts

Zhen Wang, PhD,MD

+86 34773516

wangzhen@smhc.org.cn

CONTACT