Transcranial Focused Ultrasound for Brain Modulation

DK
Overseen ByDaniel K Freeman, Ph.D.
Age: 18 - 65
Sex: Any
Trial Phase: Academic
Sponsor: Massachusetts Institute of Technology
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

There are a number of disorders of the brain that have limited treatment options, such as chronic pain, addiction, and major depression. A new technology has emerged in the last decade known as transcranial focused ultrasound, which can deliver focused acoustic signals through the skull to modulate brain activity over a small region, including structures deep in the brain. This has resulted in many ongoing clinical trials for various disorders, but there is still a lack of understanding of the optimal sonication parameters for increasing versus decreasing brain activity. The investigators aim to address this open question by sonicating the primary visual cortex and primary auditory cortex in human with a range of sonication parameters. These brain structures were chosen to target because they are expected to elicit perceptual responses in the subject (i.e., the subject will report visual and auditory perception during sonication), allowing the experimenters to infer directly the extent to which neural signals can propagate through the visual and auditory systems in a way that is sufficient to produce conscious perception. Such findings have applications not only in clinical treatments, but also in the fundamental science of the neural basis of sensory perception. Previous work has shown that sonicating the visual cortex in humans can elicit visual perception, but the ultrasonic system in prior work did not have the focusing capabilities that will be employed in this study. At the end of this study, the investigators will have determined the optimal sonication parameters that can elicit neural responses over a small volume over sensory cortex, which can be inferred from visual percepts being localized in space (e.g., a bright spot as opposed to a diffuse light), and auditory percepts that sound like pure tones rather than a broad set of frequencies (e.g., sounding like white noise or static).

Are You a Good Fit for This Trial?

Inclusion Criteria

No contraindications to magnetic resonance imaging (MRI) scans, such as claustrophobia
I am a healthy adult between 21 and 55 years old.

Exclusion Criteria

I have a history of blood vessel problems, bleeding risk, or take blood thinners.
History of head trauma with loss of consciousness
Contraindications for exposure to the high magnetic field of MRI imaging
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks
1 visit (in-person)

Baseline Testing and MRI

Informed consent, baseline visual or auditory testing, and MRI for target localization

1 day
1 visit (in-person)

Ultrasound Stimulation and EEG Recording

Ultrasound stimulation with EEG recording, including baseline and post-stimulation assessments

1 day
1 visit (in-person)

Follow-up and Structural MRI

Repeat behavioral testing and follow-up structural MRI to confirm no structural changes

1 day
1 visit (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • Transcranial Ultrasonic Neuromodulation

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Experimental: Transcranial Focused Ultrasound StimulationExperimental Treatment3 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Massachusetts Institute of Technology

Lead Sponsor

Trials
104
Recruited
12,810,000+

MIT Lincoln Laboratory

Collaborator