Overcoming Barriers to Focused Brain Stimulation with Transcranial Temporal Interference
Official title: Overcoming the Barriers to Effective Transcranial Temporal Interference Stimulation in Humans
Run by Northeastern University · NCT07593859 · Data updated 2026-11-12
This study tests a non-invasive brain stimulation method called transcranial temporal interference stimulation (TIS) to see if it can reliably influence motor cortex activity in healthy adults.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Northeastern University Academic / other |
| Locations | 1 site (Boston, Massachusetts) |
| Status | Recruiting |
| Started | February 1, 2026 |
| Main results expected | October 1, 2029 |
| Study ends | October 1, 2029 |
| Registry record updated | May 18, 2026 |
| Trial ID | NCT07593859 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Healthy adults aged 18-65 who are right-handed and free of neurological or orthopedic conditions that could affect participation.
✕Probably not a fit
Individuals with recent migraines, seizures, epilepsy, severe headaches, implanted medical devices, or skin issues on the scalp may not experience benefits and may be excluded for safety reasons.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Transcranial temporal interference stimulation (TIS) uses two high-frequency currents to create a low-frequency beat that can target deep brain areas with improved focality. In healthy adults, researchers will apply TIS to the motor cortex and use established transcranial magnetic stimulation (TMS) to measure cortical excitability in relation to the TIS waveform phase. The goal is to determine whether observed effects are driven by the beat frequency and to characterize safety and tolerability in humans. This work builds on preclinical and early human data suggesting TIS may offer targeted neuromodulation with fewer invasions than implanted devices. The study is non-invasive and focused on understanding mechanisms and feasibility rather than therapeutic outcomes.
Why it matters
Potential benefit: If successful, TIS could offer a non-invasive way to modulate deep brain regions with improved focus, potentially benefiting future treatments for neurological or psychiatric conditions.
How similar studies have gone: Previous human and animal work has shown promise for focused brain targeting with TIS, but the basic mechanisms and optimal parameters remain an area of active investigation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Free of neurological or orthopedic conditions that may impact the ability to participate. * Right-hand dominant (self-reported) * Aged 18-65 years Exclusion Criteria: * Ferromagnetic metal implants in the brain/skull or elsewhere (dental implants excluded). * Any implanted electronic device (e.g. cardiac pacemaker, cochlear implant, deep brain stimulator, medication infusion pump; vagal nerve stimulator) * Diseased or damaged skin on face or scalp * History of migraines, fainting, seizures/epilepsy, or psychiatric illness * Neurological disorder or intracranial lesion * Frequent or severe headaches * Prior adverse reaction to transcranial magnetic stimulation * Currently pregnant * Suspected or diagnosed heart problems (e.g. arrhythmia, cardiac disturbances). * Insulin-dependent diabetes * Suspected or diagnosed epilepsy or a familial history of epilepsy * Use of alcohol or recreational drugs in the prior 12 hours * Use of prescription and over the counter medications will be grounds for exclusion except for: contraceptive (birth control) drugs (e.g. those containing ethinyl estradiol and/or norethindrone), and seasonal allergy medications (e.g. cetirizine (Zyrtec), fexofenadine (Allegra), and loratadine (Claritin)).
Where it's running
-
Northeastern University
Boston, Massachusetts, United States Recruiting
Study contacts
- Principal investigator: Mathew Yarossi, PhD — Northeastern University
- Study coordinator: Joanne Hall, M.Sc.
- Email: hall.joa@northeastern.edu
- Phone: 17027828483
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.