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Clinical Trials in China / NCT06931236
Enrolling by invitation Not applicable

Clinical Efficacy and Mechanism of rTMS Based on dlPFC in the Intervention of Generalized Anxiety Disorder With Insomnia

NCT06931236 · tracked via the Priya Life Science China tracker
Sponsor
Yanghua Tian
Phase
Not applicable
Started
2024-08-01
Last updated
2025-04-17

Condition(s) studied

Generalized Anxiety Disorder (GAD)InsomniaRepetitive Transcranial Magnetic Stimulation (rTMS)

Investigational drug(s) / intervention(s)

Repetitive Transcranial Magnetic StimulationSham Repetitive Transcranial Magnetic Stimulation

Repetitive Transcranial Magnetic Stimulation: Repetitive transcranial magnetic stimulation (rTMS) can noninvasively modulate cortical activity by delivering a sequence of magnetic pulses.

Sham Repetitive Transcranial Magnetic Stimulation: Sham tDCS was delivered using the same protocol and current intensity, but it is carried out as the coil is turned away from the skull at 90°.

Study summary

To investigate the intervention effect of Repetitive Transcranial Magnetic Stimulation (rTMS) on insomnia symptoms of generalized anxiety disorder patients.

Eligibility

Sex
ALL
Min age
15 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: 1. age between 15 and 65 years; 2. clinically diagnosed with anxiety according to the Diagnostic and Statistical Manual of Mental Disorders-V (DSM-V); 3. no previous application of any insomnia pharmacological therapy for at least one week before baseline visit. Exclusion Criteria: 1. current or history of serious brain and body diseases; 2. current or history of schizophrenia, behavioral problems, post-traumatic stress disorder, mania, obsessive-compulsive disorder, and social phobia; 3. substance abuse or other comorbid psychological diseases.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Anhui Medical University Hefei Anhui

More Yanghua Tian trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06931236 on ClinicalTrials.gov ↗ ← All trials in China