Zapping the brain with gentle electricity may reveal hidden signs of consciousness
NCT ID NCT07699055
First seen Jul 13, 2026 · Last updated Jul 14, 2026 · Updated 1 time
Summary
This study investigates whether a 20-minute session of transcranial alternating current stimulation (tACS) over the front of the brain can alter brain wave patterns in people with disorders of consciousness, such as unresponsive wakefulness syndrome or minimally conscious state. Participants receive a single session of 40 Hz tACS while their brain activity is recorded with EEG before and after. The goal is to see if the stimulation changes specific brain wave patterns and whether those changes relate to behavioral signs of consciousness.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial alternating current stimulation (tACS)
- What this could lead to
- If successful, this could point toward a way to measure and potentially improve consciousness in patients with severe brain injuries.
- What could go wrong
- This is a small, early-stage study with only 31 participants. It tests a single session, so any effects may be temporary or not clinically meaningful.
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
-
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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31 people
The number who actually took part.
- Started
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Dec 2020
- Finished
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Sep 2024
- 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 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: * Adults aged 18 years or older. * Medically stable at the time of assessment. * No administration of sedative or hypnotic medication within the previous 24 hours. * Preserved wakefulness (spontaneous or elicited by stimulation) with reduced or absent awareness, consistent with Unresponsive Wakefulness Syndrome (UWS) or Minimally Conscious State (MCS). * Diagnosis confirmed by an experienced neurologist using repeated clinical assessments with the Coma Recovery Scale-Revised (CRS-R) and the Simplified Evaluation of CONsciousness Disorders (SECONDs) performed on different days and at different times during periods of wakefulness. Exclusion Criteria: * Acute phase of brain injury (within the first 28 days after injury). * Administration of sedative or hypnotic medication within the previous 24 hours. * Medical instability (e.g., active infection or hemodynamic instability). * Epileptic seizures uncontrolled despite anticonvulsant therapy. * Serious systemic illnesses that could affect the level of consciousness (e.g., sepsis or end-stage organ failure). * Brain death or coma without any evidence of wakefulness. * A previous history of developmental disorders, major neurological disorders, or severe psychiatric disorders associated with significant functional impairment.
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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
-
Medipol Mega University Hospital
Istanbul, Bağcılar, Turkey (Türkiye)
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