Brain zaps synced to your brain waves may boost depression treatment

NCT ID NCT03421808

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested whether delivering TMS pulses in sync with the brain's alpha rhythm improves depression outcomes more than standard TMS. 34 adults with depression received daily TMS over several weeks. The goal was to see if timing the pulses to when the brain is more excitable leads to higher remission rates.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Transcranial Magnetic Stimulation (TMS)
What this could lead to
If it works, this could lead to a more effective, personalized TMS treatment for depression by synchronizing pulses with the brain's natural rhythms.
What could go wrong
This is a small, early-phase trial with only 34 participants, so results may not apply widely. The approach is still experimental and may not show a clear benefit over standard TMS.

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

Phase 2/3

Runs two stages together: whether the treatment works, then large-scale confirmation.

Participants

34 people

The number who actually took part.

Started

Nov 2018

Finished

Jan 2024

Lead sponsor

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

21 to 70 years

Sex

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. Diagnosis of unipolar major depressive disorder, in a current major depressive episode, without psychotic features 2. Pretreatment Hamilton score ≥ 20 3. Age between 21 and 70 years 4. Fixed and stable antidepressant medications for 3 weeks prior and during the rTMS trial. Limit on benzodiazapenes to lorazepam (or equivalent) up to 3 mg every day 5. Moderate level of resistance to antidepressant treatment in the current episode, defined as failure of 1-4 adequate medication trials or intolerance to at least 3 trials, and duration of current episode ≤ 3 years 6. No history of schizophrenia, schizoaffective disorder, other \[non mood disorder\] psychosis, depression secondary to a medical condition, mental retardation, substance dependence or abuse within the past year (except nicotine), bipolar disorder, psychotic features in this or previous episodes, amnestic disorder, dementia or MMSE ≤24, delirium, obsessive compulsive disorder, post-traumatic stress disorder, panic disorder 7. No current Vagus Nerve Stimulation 8. No history of failing to respond to an adequate course of ECT in this or any episode, and no ECT within the past 3 months 9. No contraindication to MRI 10. No contraindication to rTMS (history of neurological disorder or seizure (except induced by ECT), increased intracranial pressure, brain surgery, or head trauma with loss of consciousness for \>15 minutes, implanted electronic device, metal in the head, or pregnancy) 11. No history of autoimmune, endocrine, viral, or vascular disorder. No unstable cardiac disease, uncontrolled hypertension, or sleep apnea 12. No active suicidal intent or plan, or history of attempt within the past 12 months 13. Willing to provide informed consent Exclusion Criteria: 1. To ensure that baseline levels of depression severity are stable at the time of study enrollment, patients will be dropped if they show \> 30% improvement in the HRSD score from the time of initial intake (e.g., screening) to the baseline assessment. 2. Patients must have a recordable alpha frequency.

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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

  • Medical University of South Carolina Brain Stimulation Division

    Charleston, South Carolina, 29425, United States

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