Healthy volunteers, healthy participants, no condition Healthy volunteers, healthy participants, no condition
Conditions
Interventions
Temporal interference stimulation involves the application of two high-frequency sinusoidal currents (carriers) with slightly different frequencies through skin electrodes, producing an amplitude-modu
Sponsors
Eindhoven University of Technology
Eligibility
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: Healthy adult between 18 and 64 years old, Right-handed
Exclusion criteria
Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study:History of head injury or craniotomyPersonal or family history of neurological or psychiatric disordersMetal implants or implanted electronic devicesSkin sensitivity or allergies that may interfere with stimulationUse of medication during the time of the experimentCurrent pregnancy or possibility of being pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the change in EEG power at 5 Hz during stimulation compared to baseline and control. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary parameters include EMG burst amplitude and spectral power at stimulation frequencies, as well as EEG responses across other stimulation conditions (e.g., 20 Hz envelope). Comparisons between different carrier and envelope frequency conditions will be performed. | — |
Countries
Netherlands
Contacts
Public ContactR.M.C. Mestrom
Eindhoven University of Technology
Outcome results
None listed