Actively Recruiting
TMS for Anxiety and Trauma-related Disorders
Led by Shanghai Mental Health Center · Updated on 2024-07-10
15
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
Sponsors
S
Shanghai Mental Health Center
Lead Sponsor
B
Brigham and Women's Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The present pilot study will apply accelerated intermittent theta burst stimulation (aiTBS) to a novel transcranial magnetic stimulation (TMS) target for anxiety derived via causal network mapping.
CONDITIONS
Official Title
TMS for Anxiety and Trauma-related Disorders
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of generalized anxiety disorder, social anxiety disorder, panic disorder, and/or post-traumatic stress disorder as defined by DSM-5 criteria
- Male or female between 18 and 60 years old
- Right-handed
- Able to understand and sign an informed consent document
- Beck Anxiety Inventory score of 16 or higher
- On a stable medication or psychotherapy regimen for at least 6 weeks before the study and throughout its duration
- In good general health based on medical history
- History of resistance to pharmacological or psychotherapeutic treatment
You will not qualify if you...
- Substance use disorders, eating disorders, significant suicidal thoughts, mental disorder due to medical or neurocognitive condition, lifetime psychosis, bipolar disorder, developmental disorders
- History of brain surgery or epilepsy
- Presence of metallic foreign bodies like pacemakers or stents
- Any medical condition or medication that increases seizure risk
- Pregnancy
- Intellectual disability
- Current severe physical illnesses such as cancer, heart failure, or pneumonia
- Severe claustrophobia preventing MRI use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shanghai Mental Health Center
Shanghai, Shanghai Municipality, China, 200030
Actively Recruiting
Research Team
H
Huiru Cui, Ph.D
CONTACT
J
Jijun Wang, Ph.D
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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