Actively Recruiting

Phase 1
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT07219719

Temporal Interference for Thalamocortical Activity and Network Modulation

Led by University of Wisconsin, Madison · Updated on 2026-04-22

40

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to find out whether a type of electrical brain stimulation, called temporal interference stimulation, can temporarily change the way different parts of the brain communicate with each other. Participants will: * Complete two stimulation phases - overnight and during wakefulness * Undergo two MRIs per study phase

CONDITIONS

Official Title

Temporal Interference for Thalamocortical Activity and Network Modulation

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18-50
  • Medically healthy
  • U.S. citizen or permanent resident
  • English-speaking
Not Eligible

You will not qualify if you...

  • Current or past neurological disorders or acquired neurological disease, including intracranial lesions
  • History of inpatient psychiatric hospitalization
  • Head trauma with prolonged loss of consciousness or more than three grade I concussions
  • Poorly controlled headaches or migraines
  • Systemic illness or unstable medical condition that may cause emergency with provoked seizure
  • History of seizures, epilepsy, abnormal EEG, or family history of treatment resistant epilepsy (except single benign seizure)
  • Possible pregnancy or plan to become pregnant in next 6 months
  • Any metal in the head
  • Medical devices or implants such as pacemakers, pumps, cochlear implants, or nerve stimulators
  • Dental implants or permanent retainers
  • Hair braids, dreadlocks, hair pieces, or extensions that cannot be removed before study
  • Unwillingness to remove head coverings for study sessions
  • Medications that may alter seizure threshold including specific stimulants, antidepressants, SSRIs, antipsychotics, bronchodilators, antibiotics, antivirals, antihistamines, or estradiol-based birth control
  • Claustrophobia
  • Back problems preventing lying flat for up to two hours
  • Regular night-shift work
  • Sleep apnea or other sleep disorder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Wisconsin - Madison

Madison, Wisconsin, United States, 53705

Actively Recruiting

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Research Team

S

Sean Prahl

CONTACT

L

Larissa Albantakis, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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