Electrophysiological Source Imaging Guided Transcranial Focused Ultrasound

ConditionHealthy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-64
SponsorCarnegie Mellon University

About this trial

Neuromodulation is a fast growing field that offers a wide range of applications for both understanding and treating the brain. Future research for non-invasive neuromodulation will need to elucidate the optimal frequency, duration, and intensity of stimulation for a variety of technologies and diseases. Closed loop stimulation is thus a promising research area that allows for responsive stimulation and real time symptom management. Our project is proposed to develop and test a novel noninvasive neuromodulation integrating transcranial focused ultrasound stimulation (tFUS) with electrophysiological source imaging (ESI-tFUS) to allow evidence-based neuromodulation for brain research and the management of brain conditions. Despite the recent developments and attention surrounding tFUS, relatively little is known about the mechanisms and optimal parameters of this stimulation technology. The addition of ESI neuroimaging, aimed at providing biomarkers to assess the effects of tFUS neuromodulation, could provide crucial necessary information regarding the neural response to the applied stimulation in real-time. In order for tFUS to be further developed and transformed into a robust neuromodulation technology, an integrated electrophysiological source-imaging-guided tFUS system to allow for individualized and responsive stimulation is needed.

The purpose of this study is to develop and evaluate the proposed ESI-tFUS in human subjects using motor and somatosensory paradigms.

Eligibility criteria

Qualifiers

Apparently healthy volunteers.

Age 18-64.

Willing and able to provide written consent.

Able to communicate in the English language.

Disqualifiers

Evidence of a current significant medical illness or psychiatric or central or peripheral neurologic disorder

History of loss of consciousness of more than ten minutes in the past year or loss of consciousness in a lifetime that required rehabilitation services

Personal or family history of seizure

Any history of stroke/transient ischemic attack (TIA)

Trial design

Treatments tested in this trial

  • Ultrasound

Treatment groups

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Carnegie Mellon University

Lead sponsor

University of Minnesota

Sponsor institution