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Study identifier: NCT07121712 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Navigated cTBS for the Treatment of Generalized Anxiety Disorder

Condition: Generalized Anxiety Disorder  ·  Sponsor: WANG KAI

PhaseNA
Planned participants40
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The purpose of this study is to investigate the effectiveness of a non-invasive brain stimulation technique called continuous Theta Burst Stimulation (cTBS) for treating Generalized Anxiety Disorder (GAD). The researchers will use a neuronavigation system, which acts like a GPS for the brain based on a participant's own MRI scan, to guide the stimulation to a specific target in the brain's auditory association cortex. This area is involved in processing information and may play a role in anxiety. Participants who enroll will be randomly assigned to one of two groups. One group will receive active cTBS treatment, while the other will receive a sham (placebo) stimulation that feels similar but has no therapeutic effect. The treatment will be given three times a day for seven consecutive days. Before and after the treatment period, all participants will complete clinical questionnaires to measure their anxiety and related symptoms. They will also undergo Magnetic Resonance Imaging (MRI) scans to help researchers understand how cTBS affects brain activity. A follow-up assessment will be conducted two weeks after the treatment ends to check on symptoms.

This description comes directly from the study's public registry record.

Talk to the study team

Kai Wang, MD  ·  +86-0551-62923704  ·  wangkai1964@126.com

Tongjian Bai, MD  ·  baiyunong1990@163.com

Always discuss trial participation with your own doctor first.

Locations (2)

Anhui Medical UniversityHefei, Anhui, ChinaRecruiting
Anhui Medical UniversityHefei, Anhui, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07121712