Electroacupuncture for Generalized Anxiety Disorder: Clinical Efficacy and Neuroimaging Mechanisms

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorLishu Gao

About this trial

This study aims to evaluate the clinical efficacy and safety of electroacupuncture (EA) in treating Generalized Anxiety Disorder (GAD). Participants will be randomly assigned to an EA group, a sham EA group, or a waiting-list control group. All participants will continue their routine medication (Paroxetine). The primary goal is to observe the reduction in anxiety symptoms using the Hamilton Anxiety Scale (HAMA). Additionally, the study will use functional MRI (fMRI) and Magnetic Resonance Spectroscopy (MRS) to explore the brain mechanisms through which EA helps alleviate anxiety.

Eligibility criteria

Qualifiers

Meet the DSM-5 diagnostic criteria for Generalized Anxiety Disorder (GAD).

No antidepressant or anti-anxiety medication in the past 2 weeks.

HAMA score ≥ 14.

Right-handed(for MRI).

Disqualifiers

Complicated with severe cardiovascular, cerebrovascular, or organic diseases.

History of other psychiatric disorders (e.g., schizophrenia, bipolar disorder).

Contraindications for MRI (e.g., metal implants, claustrophobia).

Pregnancy or lactation.

Trial design

Treatments tested in this trial

  • Electroacupuncture (EA)
  • Sham Electroacupuncture (SEA)
  • Routine Medication

Treatment groups

123 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Lishu Gao

Lead sponsor

First People's Hospital of Hangzhou

Sponsor institution