Skip to content

Effects of bioelectric technology combined with antidepressant therapy in anxiety patients

Effects of bioelectric technology combined with antidepressant therapy in anxiety patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051156
Enrollment
Unknown
Registered
2021-09-15
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-23

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

Conditions

Anxiety disorders

Interventions

Experimental group1:Low frequency electrophysiological therapy
Experimental group2:Antidepressant medication
control group:None

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for anxiety disorders in the American Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM-5); 2. HAMA (14 items) score > 21 points; HAMD (24 items) > 20 points; 3. Aged 18 to 65 years, no gender limit; 4. Have more than 6 years of education and be able to complete the assessment of the scale under guidance; 5. Agree to participate in this study and sign the informed consent; 6. Healthy control group: healthy people without mental illness, no history of mental illness or major physical illness in the past.

Exclusion criteria

Exclusion criteria: 1. There are contraindications to electrical stimulation therapy: patients with severe heart failure, those with synchronized cardiac pacemakers in the chest, the abdomen of pregnant women, patients with obvious bleeding tendency at the surgical trauma site, thrombotic peripheral vascular disease, malignant tumor areas, neurological diseases; 2. Patients with serious physical diseases such as cardiovascular, lung, liver, kidney, endocrine, blood system, etc.; 3. Patients who are unable to cooperate in completing the research content are evaluated by the investigator.

Design outcomes

Primary

MeasureTime frame
Depression;Anxiety;

Countries

China

Contacts

Public ContactRen Huipeng

The First Hospital of Hebei Medical University

renhuipeng@126.com+86 13833125871

Outcome results

None listed

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