RecruitingNot ApplicableNCT07022171

Mechanisms of Transcutaneous Auricular Vagus Nerve Stimulation in Depression

Physiological and Molecular Mechanisms of Transcutaneous Auricular Vagus Nerve Stimulation in Depression


Sponsor

Max-Planck-Institute of Psychiatry

Enrollment

86 participants

Start Date

Mar 18, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Invasive vagus nerve stimulation (VNS) is an approved treatment of treatment-resistant depression (TRD) in Europe and in USA. Because of the associated possible surgical complications as well as side effects, invasive VNS is applied limitedly in the treatment of depression. Transcutaneous auricular VNS (tVNS), on the other hand, is a non-invasive alternative to traditional invasive VNS. tVNS is still considered an experimental treatment for depression. This is due to the limited high-quality evidence from randomized clinical studies, the not yet fully understood biological mechanisms of action, along with overall limited knowledge about the optimal stimulation parameters. To address these issues, the AddVNS study was initiated. The AddVNS study intends to recruit n=86 patients of the Max Planck Institute of Psychiatry with depression. The patients participating in the AddVNS study are going to receive either tVNS or sham tVNS for a period of 6 weeks. The primary objective of the study is to identify biological, psychological, socio-economic, and clinical biomarkers associated with treatment progression and response to treatment in patients with depression undergoing tVNS. To achieve this, an exploratory design with an assessment of many different parameters including psychophysiology, imaging, blood-based multi-omics, microbiome, psychometrics and neuropsychology will be used.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a gentle, non-invasive form of nerve stimulation called transcutaneous auricular vagus nerve stimulation (taVNS) — delivered through a small device worn on the ear — to see if it can reduce depression symptoms in people with major depressive disorder or bipolar depression. **You may be eligible if...** - You are between 18 and 65 years old - You have been diagnosed with a depressive episode as part of major depressive disorder or bipolar disorder (DSM or ICD criteria) - You are using a reliable contraceptive method if applicable **You may NOT be eligible if...** - You are pregnant, planning to become pregnant, or breastfeeding - You have a severe neurological condition (e.g., epilepsy, dementia) - You have a developmental disability or significant intellectual impairment - You have active substance abuse (alcohol or drugs) - taVNS cannot be applied to your ear for physical or medical reasons Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEtranscutaneous auricular vagus nerve stimulation

Half of the patients are randomized to the arm receiving transcutaneous auricular vagus nerve stimulation for a period of six weeks. Transcutaneous auricular vagus nerve stimulation will be carried out as an adjuvant, i.e. in addition to the regular treatment of the participants. The intervention will take place three times a day from Monday to Friday. Each of the three daily sessions is going to last 30-60 minutes, depending on patient tolerance.

DEVICEsham transcutaneous auricular vagus nerve stimulation

Half of the patients are randomized to the arm receiving sham transcutaneous auricular vagus nerve stimulation for a period of six weeks. Sham transcutaneous auricular vagus nerve stimulation will be carried out as an adjuvant, i.e. in addition to the regular treatment of the participants. The intervention will take place three times a day from Monday to Friday. Each of the three daily sessions is going to last 30-60 minutes. The procedures for sham tVNS will be identical to tVNS, with the only exception that the sham tVNS will be performed with no current output


Locations(1)

Max Planck Institute of Psychiatry

Munich, Germany

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NCT07022171


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