Could flickering lights and tones ease schizophrenia?
NCT ID NCT07342465
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early study tests whether a device that delivers synchronized 40 Hz light and sound (called GENUS) is safe and feasible for people with schizophrenia. The goal is to see if this at-home stimulation can improve brain rhythms, thinking, and symptoms that current medications don't fully address. Twenty participants will receive one hour of stimulation and undergo brain scans and cognitive tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Gamma Entrainment Using Sensory Stimulation (GENUS) device delivering synchronized 40 Hz light and sound
- What this could lead to
- If it works, this could point toward a safe, at-home treatment to ease cognitive and negative symptoms of schizophrenia that current drugs often miss.
- What could go wrong
- This is a very early, small trial (20 people) focused on safety and feasibility, not proof of effectiveness. The benefits seen may not hold up in larger studies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- 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 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Between 18-65 years of age. 2. A diagnosis of schizophrenia or schizoaffective disorder 3. No medication is an absolute exclusion. Medications will be reviewed by the responsible MD and a decision about inclusion will be made based on the following: the patient's past medical history, drug dose, history of recent medication changes or duration of treatment, and combination with other CNS (central nervous system) active drugs. 4. The subject is willing to sign the informed consent document. 5. If the subject is deemed not to have the capacity to sign the informed consent, he/she will need a legally authorized representative to provide surrogate consent. Exclusion Criteria: 1. Subjects who do not have healthcare 2. MRI contraindications such as the presence of pacemakers, aneurysm clips, artificial heart valves, ear implants, metal fragments, or foreign objects in the eyes, skin or body. 3. High myopia \< -7 diopters, or untreated cataracts that affect vision. 4. Clinical conditions: 1. History of seizure or medical diagnosis of epilepsy. 2. ECT history \> 6 months 3. Female subjects who are pregnant or currently breastfeeding. 4. Longstanding premorbid history (i.e., longer than 10 years) of alcohol or substance abuse with continuous abuse up to and including the time that the symptoms leading to clinical presentation developed. 5. Significant neurological or medical disorders that may produce cognitive impairment. 6. Profound hearing or visual impairment. 7. Eye surgery in the last 3 months or are scheduled to have eye surgery in the next 3 months (during the study)
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Massachusetts Institute of Technology (MIT)
Cambridge, Massachusetts, 02139, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Scientists probe brain's reward system in mental illness
- Can talk therapy and social coaching ease early psychosis?
- Brain training may reshape brain chemistry in schizophrenia
- Could a single daily dose of clozapine work just as well?
- A gentle brain zap might boost medication adherence in schizophrenia
- Can sound and light waves calm the mind in schizophrenia?