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The SEAS Study: Sensory Engagement and Activation During Noninvasive Stimulation

RecruitingHealthy volunteers welcome

Who can join

Ages 18 to 65 · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

* Able to provide written informed consent in English.
* Willing and able to complete study procedures (e.g., \~1-hour sessions with non-invasive recordings, \~3-hour visit).

Exclusion Criteria:

* History of neurological disorders (e.g., epilepsy, migraines) or psychiatric conditions requiring medication.
* Active implanted medical devices (e.g., pacemakers, cochlear implants) or metal in the neck/forearm that could interfere with stimulation or recordings.
* Skin conditions or open wounds at stimulation sites (cervical neck, forearm).
* Women who are pregnant or breastfeeding.
* Current use of medications affecting autonomic or cortical function (e.g., beta-blockers, sedatives).
* Inability to sit still for recordings or understand instructions (e.g., due to severe vision/hearing impairment).

About the study

Early feasibility study to establish quantitative physiological markers correlated with noninvasive stimulation.

What is being tested

Sponsor: University of Minnesota · Participants: 40 · Started: Jun 8, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07606573

Locations in the U.S.

MinnesotaM Health Clinical Research Unit, Minneapolis
M Health Clinics and Surgery Center and satellite Neurology Clinic locations, Minneapolis
Translational Neurotechnology (TNT) Lab, Minneapolis

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.