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Effect of transcutaneous auricular vagus nerve stimulation combined with high-definition transcranial direct current stimulation on major depressive disorder

Effect of transcutaneous auricular vagus nerve stimulation combined with high-definition transcranial direct current stimulation on major depressive disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096753
Enrollment
Unknown
Registered
2025-02-06
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

Major depressive disorder

Interventions

taVNS group:taVNS+ sham HD-tDCS, continuous intervention for two weeks, 5 days a week
HD-tDCS group:sham taVNS+HD-tDCS, continuous intervention for two weeks, 5 days a week
Sham group:sham taVNS+sham HD-tDCS, continuous intervention for two weeks, 5 days a week
Combination group:taVNS+HD-tDCS, continuous intervention for two weeks, 5 days a week

Sponsors

Hangzhou Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Outpatient or inpatient patients aged 18-45 (including 18 and 45 years old), regardless of gender; (2) Primary school education or above; (3) Meets the diagnostic criteria for major depressive disorder episodes in DSM-5, single episode or recurrent episode; (4) Hamilton Depression Rating Scale (HAMD-24) score >= 20 points; (5) Stable use of an SSRI antidepressant for >= 2 weeks (6) Understand and voluntarily participate in this study, be able to follow the treatment process, and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Meet the diagnostic criteria for other mental disorders in DSM-5, such as post-traumatic stress disorder, neurocognitive disorders, schizophrenia, bipolar disorder, alcohol (or drug) dependence or abuse, personality disorders, etc; (2) Depressive episodes secondary to a systemic or neurological disorder; (3) Serious physical illnesses, such as heart, liver, and kidney dysfunction, impaired respiratory function, severe infections, etc; (4) Any serious neurological disease or damage, including but not limited to space occupying brain injury, history of epileptic seizures, Parkinson's disease, multiple sclerosis, severe head trauma; (5) Implanting electronic devices such as pacemakers and cochlear implants into the body; (6) Pregnant or lactating patients; (7) Received other neuroregulatory treatments such as MECT or rTMS within the past 3 months; (8) Individuals with autoimmune diseases such as systemic lupus erythematosus and rheumatoid arthritis, or with upper respiratory tract infections or other infectious diseases within 2 weeks prior to enrollment; (9) HAMD-24 score >= 3 in item 3, or those who currently or in the past 12 months have a clear tendency towards suicide, and are considered at risk of suicide and violent behavior based on the researcher's clinical assessment.

Design outcomes

Primary

MeasureTime frame
Depressive degree;Inflammatory indicators;

Secondary

MeasureTime frame
Anxiety degree;Depressive symptoms;Anxiety symptoms;Suicidal ideation;Clinical symptoms;Sleep quality;Sleep rhythm;Brain function;Heart rate variability;Cognitive function;Sex hormone;

Countries

China

Contacts

Public ContactDeng Wei

Hangzhou Seventh People's Hospital

dengw@zju.edu.cn+86 134 8403 6877

Outcome results

None listed

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