RM1 Project 2 - tAN fMRI Study

This study is looking at a treatment called transcutaneous auricular neurostimulation (tAN), which uses gentle electrical stimulation on your ear. This stimulation targets specific nerves (the auricular branch of the vagus nerve and the auriculotemporal nerve) that may help with chronic pain. We want to see if stimulating both nerves at the same time has a stronger effect on your brain activity compared to stimulating just one nerve. We'll measure these brain changes using an fMRI (functional magnetic resonance imaging) scan while you receive the stimulation. You can join if you are between 18 and 65 years old and can give your own consent. We are looking for 96 participants for this study.

Study design
This is a randomized, double-blind, sham-controlled study involving 96 participants. It compares different types of electrical stimulation on the ear.
What's involved
You would participate in one visit where you receive electrical stimulation through electrodes on your ear while undergoing an fMRI scan.
Compensation
Not stated in the trial record.
Follow-up
Brain activity will be measured during the tAN stimulation. No follow-up after this period is specified.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT05487664

RM1 Project 2 - tAN fMRI

Recruiting
NAAges 18–65InterventionalTreatment
Medical University of South Carolina
~96 participants
Updated 2025-12-18 on ClinicalTrials.gov
What's tested:Transcutaneous Auricular Neruostimulation (tAN)

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
BOLD signal changes during stimulation relative to no stimulation
Measured over During tAN
Auricular Stimulation

NCT05487664

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Medical University of South Carolina Institute of Psychiatry

    Charleston, South Carolinastudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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Eligibility criteria

Inclusion

Age 18-65
Have the capacity and ability to provide one's own consent and sign the informed consent document

Exclusion

Contraindicated for MRI.
Any current or recent untreated medical, neurological, or psychiatric conditions
Metal implant devices in the head, heart or neck.
History of brain surgery.
History of myocardial infarction or arrhythmia, bradycardia.
Personal or family history of seizure or epilepsy or personal use of medications that substantially reduce seizure threshold (e.g., olanzapine, chlorpromazine, lithium).
Personal history of head injury, concussion, or self-report of moderate to severe traumatic brain injury.
Individuals suffering from frequent/severe headaches.
Individuals with a reported history of psychosis or mania, or individuals who are actively manic or psychotic.
Moderate to severe alcohol or substance use disorder.
Pregnancy
  • BOLD signal changes during stimulation relative to no stimulationDuring tAN

    . tAN will will be administered to participants within the bore of the MRI scanner while we acquire high resolution functional neuroimaging. Both a general linear model and SNM approach will be used to examine BOLD signal changes during stimulation relative to rest blocks, comparing each of the four stimulation targets within- and between subjects to determine whether stimulating two cranial nerves produces a more robust neurophysiological effect than either single nerve or sham stimulation alone.