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Vagus Nerve Stimulation for Reaction Time

Enhancing Reaction Time Through Non-Invasive Vagus Nerve Stimulation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07528742
Enrollment
30
Registered
2026-04-14
Start date
2026-04-06
Completion date
2027-04-05
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Subjects (HS)

Brief summary

Non-Invasive Vagus Nerve Stimulation will be provided to the participants using a transcutaneous electrical nerve stimulation (TENS) unit, a routine physical therapy intervention by the faculty researcher who is a licensed physical therapist. The electrodes will be clipped to ear over the vagus nerve distribution area. The parameters will be 30 Hz, 250 us, 5 minutes, at tolerance (no pain). Reaction time will test collected pre and post the stimulation using online reaction time testing platform.

Interventions

DEVICEvagus nerve stimulation

Non-Invasive Vagus Nerve Stimulation will be provided to the participants using a transcutaneous electrical nerve stimulation (TENS) unit, a routine physical therapy intervention by the faculty researcher who is a licensed physical therapist. The electrodes will be clipped to ear over the vagus nerve distribution area. The parameters will be 30 Hz, 250 us, 5 minutes, at tolerance (no pain)

Sponsors

Youngstown State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy participants over the age of 18 * did not receive vagus nerve stimulation previously

Exclusion criteria

* alcohol or drug abuse * metal in the skull * implanted cardiac or cranial devices * Women during 3 trimester of pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Reaction timeBaseline and immediately after the intervention.Reaction time will test collected pre and post the stimulation using online platform. The subjects will press a key when setting a color change in the computer screen.

Countries

United States

Contacts

CONTACTWeiqing Ge Ge, DPT, PhD
wge@ysu.edu330-941-2702

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026