Brain zaps for the blues: new study tests Quick-Pulse therapy
NCT ID NCT05436379
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a type of brain stimulation called theta burst stimulation (TBS) to see if it could reduce depression symptoms. 21 adults with current depression received the treatment, and some also got positive affect training. The main goal was to measure changes in depression severity using a standard rating scale.
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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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21 people
The number who actually took part.
- Started
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Jun 2022
- Finished
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Nov 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 26 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.
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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: * Current Diagnostic and Statistical Manual (DSM-5) Depressive Disorder Exclusion Criteria: * Bipolar disorder (lifetime) * Obsessive-compulsive disorder (lifetime) * History of psychosis * Daily use of nicotine * Past-month use of cocaine, amphetamines, Methyl enedioxy methamphetamine (MDMA), Phencyclidine (PCP), Ketamine, or gamma-hydroxybutyrate (GHB) * Past 6 month substance use disorder * Binge drinking (using NIAAA criteria) within the past week, alcohol use in the past 12 hours * Neurological disorders: Epilepsy, Parkinson's Disease, brain tumor, brain injury, stroke * History of head trauma with a loss of consciousness (e.g., concussion) * History of seizures * MRI contraindications: body shape/size too large to fit in scanner, claustrophobia, and ferromagnetic metal in the body * Pregnancy * Current use of Clozapine, Bupropion, or prescription stimulants * Current use of benzodiazepines or mood stabilizers * Body shape/size too large to fit in MRI scanner * Claustrophobia * Metal in the head or ferromagnetic metal in the rest of the body * Implanted medical devices * High-risk suicidality
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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 University of Pittsburgh, Department of Psychiatry
Pittsburgh, Pennsylvania, 15213, United States
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Other studies related to the condition(s) this trial covers.
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