Wearable ultrasound gadget zaps brain to boost dream sleep
NCT ID NCT07190287
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a wearable system that records brain waves and delivers gentle ultrasound to deep brain areas during REM sleep. Fifty-two healthy adults and people with mild sleep or stress issues wore the device for two nights. The goal was to see if it safely increases REM sleep and improves stress-related measures, helping guide future sleep therapies.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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52 people
The number who actually took part.
- Started
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Jul 2025
- Finished
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Oct 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria for Healthy Volunteers: \- Adults aged 18-50, willing and able to undergo MRI, EEG, and FUS experiments. Inclusion Criteria for Healthy Volunteers with Non-Clinical Sleep Disturbances: * Adults aged 18-50, willing and able to undergo EEG and FUS experiments. * Pittsburgh Sleep Quality Index (PSQI) score between 5 and 10. * Perceived Stress Scale (PSS) score between 16 and 21. Exclusion Criteria for Both Groups: * Current or past history of psychopathology, epilepsy, or other seizure disorders. * Inability to provide informed consent to undergo EEG recording, FUS stimulation, and MRI. * Diagnosed sleep disorders (e.g., insomnia, obstructive sleep apnea). * Contraindications to FUS or MRI, including but not limited to: history of stroke, brain tumors, brain hemorrhages, internal wires, electrodes, pacemakers, implants, irremovable ferromagnetic objects in the head that are unsafe for MRI and/or cause large imaging artifacts, brain surgery, moderate-to-severe head injury, any penetrating head injury, or uncontrolled thyroid disorder. * Pregnant individuals or those attempting to become pregnant (due to unknown MRI-related risks to fetuses). * Serious medical illnesses likely to interfere with study participation. * Current active suicidal or homicidal ideation (or suicide attempt within the past 3 months). * Current substance use disorder. * Current or recent (within the past 3 months) psychotic symptoms. * Currently meeting diagnostic criteria for a manic episode. * Currently engaged in evidence-based or experimental treatments (e.g., weekly cognitive behavioral therapy, transcranial magnetic stimulation, ketamine/esketamine treatment) other than psychiatric medications that have been on a stable dosage and regimen for at least 3 months (including antidepressants, mood stabilizers, atypical antipsychotics, and sedatives/hypnotics), in order to avoid confounding therapeutic effects.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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UT Austin, Biomedical Engineering Department
Austin, Texas, 78712, United States
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Other studies related to the condition(s) this trial covers.
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