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A clinical study of the efficacy of amygdala temporal interference electrical stimulation therapy in patients with anxiety disorders

A clinical study of the efficacy of amygdala temporal interference electrical stimulation therapy in patients with anxiety disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101289
Enrollment
Unknown
Registered
2025-04-23
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Generalized anxiety disorder

Interventions

Time interferes with the stimulus group:Time Interference Stimulation Therapy
Fake stimulation group:Time interference stimulation therapy

Sponsors

The first affiliated hostipal of nanchang university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age is between 18 and 65 years old (inclusive of the boundary values); 2.Patients with a clinical diagnosis of anxiety disorder; 3.The dose of anti-anxiety therapy was stable for 6 weeks prior to the implementation of the study.

Exclusion criteria

Exclusion criteria: 1.Has significant central nervous system dysfunction other than anxiety disorder; 2.History of epilepsy or EEG detection of epileptiform activity; 3.A pacemaker is implanted in the body; 4.Metal insets in the skull or in the mouth and neck; 5.Claustrophobia.

Design outcomes

Primary

MeasureTime frame
MJMRI data;EEG data;

Secondary

MeasureTime frame
Baker Anxiety Scale score;

Countries

China

Contacts

Public ContactMengqian li

The first affiliated hostipal of nanchang university

limengqian@126.com+86 791 88692280

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026