The SEAS Study: Sensory Engagement and Activation During Noninvasive Stimulation

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Healthy Adult Participants

In brief

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

Key facts

Study ID

NCT07606573

Run by

University of Minnesota

People needed

40

Starts

2026-06-08

Expected to finish

2028-02-01

Last updated by the study team

2026-06-11

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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).

You may not qualify if…

• 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).

Where it is running

• M Health Clinical Research Unit — Minneapolis, Minnesota, United States (enrolling)
• M Health Clinics and Surgery Center and satellite Neurology Clinic locations — Minneapolis, Minnesota, United States (enrolling)
• Translational Neurotechnology (TNT) Lab — Minneapolis, Minnesota, United States (enrolling)

Full record on ClinicalTrials.gov

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