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Study details
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Noninvasive Vagal Nerve Stimulation Trial

NYU Langone Health
NCT IDNCT06816004ClinicalTrials.gov data as of Apr 2026
Target enrollment

30

Study length

about 9 months

Ages

25–65

Locations

1 site in NY

What this study is about

This trial is testing whether remotely supervised transcutaneous auricular vagus nerve stimulation (taVNS), transcutaneous cervical vagus nerve stimulation (tcVNS), or transcranial direct current stimulation (tDCS) can help reduce symptoms in people with multiple sclerosis. The goal of this pilot trial is to determine if these treatments are feasible and may improve symptom reduction, as measured by self-reported outcomes and heart rate variability.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Use Remotely Supervised Transcranial Direct Current Stimulation (RS - tDCS)
  • 2.Use Remotely Supervised Transcutaneous Auricular Vagus Nerve Stimulation (RS - taVNS)
  • 3.Use Remotely Supervised Transcutaneous Cervical Vagus Nerve Stimulation (RS - tcVNS)

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized (Open Label)

You are randomly assigned, but you will know your treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: Change in Composite Autonomic Symptom Score-31 (COMPASS-31) Score, Change in General Anxiety Disorder (GAD-7) Score, Change in Heart Rate Variability (HRV), Change in Memorial Symptom Assessment Scale (MSAS) Score, Change in PROMIS Fatigue - Short Form 7a Score, Change in PROMIS Pain Intensity - Short Form 3a Score, Change in Patient Health Questionnaire (PHQ-9) Score, Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Disturbance - Short Form Score

Devices

therapeutic

Body systems

Neurology