New brain zapping technique shows promise for depression
NCT ID NCT05224206
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how a fast form of brain stimulation called iTBS affects the brains of 22 adults with major depression. Participants receive both real and fake stimulation in a blinded setup, followed by 6 weeks of daily treatment. The goal is to understand how iTBS changes brain activity and whether it can reduce depression symptoms.
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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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About 22 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2023
- Expected to finish
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Jan 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 55 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: * Men or women aged 18 to 55 years of age * Mini-International Neuropsychiatric Interview-confirmed diagnosis of MDD, as a single or recurring episode * Symptoms of MDD have not improved after ≥ 1 but ≤ 7 adequate dose(s) of antidepressant trial(s) in the current depressive episode * A baseline score of ≥ 15 on the 17-item Hamilton Rating Scale for Depression (HRSD-17) * Have received a stable antidepressant regimen for at least four weeks prior to entering trial * Are voluntary and competent to consent to study * Can speak and read English Exclusion Criteria: * Current or past (\< 3 months) substance (including nicotine) or alcohol abuse/dependence, as defined in DSM-5 criteria * Positive urine test for illegal substances, cannabis, or cotinine * Suicide attempt in the past three months and/or active suicidal intent * Pregnancy (confirmed by urine test) and/or lactation * Psychotic features in the current episode * Any comorbid mental health disorders (including, but not limited to lifetime history of psychotic disorders, OCD, PTSD and/or bipolar I or II disorder) with the exception of anxiety/panic disorders and ADHD * Significant unstable medical or neurologic illness confirmed by medical history and blood test at baseline (e.g. uncontrolled diabetes, or renal dysfunction) * Organic cause to the depressive symptoms (e.g. thyroid dysfunctions), as ruled out by the referring physician * Contraindication for TMS (e.g., personal history of epilepsy or convulsion, metallic head implant, pacemaker) * Contraindication for MRI (e.g. metallic implant, claustrophobia) * Have undergone a prior PET or SPECT research study * ECT or rTMS treatment in the current depressive episode * Benzodiazepine use * Have a body mass index (BMI) higher then 35 or lower then 18 * Any other condition that, in the opinion of the investigators, would adversely affect the participant's ability to complete 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.
Contacts and locations
Locations
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The Royal Ottawa Mental Health Centre
Ottawa, Ontario, K1Z 7K4, Canada
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Other studies related to the condition(s) this trial covers.
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