Optimizing Brain Excitability in Depression
Stanford University · with National Institute of Mental Health (NIMH) · NCT07242105
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 145
- US sites recruiting
- 2
- Study start
- October 23, 2025
- Record last updated
- February 10, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The goal of this study is to improve depression treatment by establishing reliable prefrontal excitability markers through Targeting with Automated Real-time Guidance for Enhancing TEPs (TARGET).
Being studied: Active Single-Pulse TMS; Sham Single-Pulse TMS; TARGET-optimized TMS; Non-optimized (Open-Loop) TMS; EEG Recording; Intracranial EEG (iEEG) Recording
Conditions: Major Depressive Disorder
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Men and women, ages 18 to 65
- Diagnosis of major depressive disorder, assessed through a Structured Clinical Interview for DSM-5 (SCID-5)
- In a current depressive episode, assessed through a Structured Clinical Interview for Diagnostic and Statistical Manual of Mental Disorders (DSM-5) (SCID-5)
- Moderate-to-severe depression as indicated by a score between 11-20 on the Quick Inventory of Depressive Symptoms (QIDS)
- Must comprehend English well to ensure adequate comprehension of the EEG and TMS instructions, and of clinical scales
- No current or history of neurological disorders
- No seizure disorder or risk of seizures
- Neurosurgical patients: Men and women ages 18-65 with medication-refractory epilepsy who are admitted for phase II intracranial monitoring to detect a seizure focus will be considered appropriate for this study. Participants must have the intellectual capacity to understand the consent process and agree to the study.
Exclusion Criteria
- Those with a contraindication for MRIs (e.g. implanted metal)
- History of head trauma with loss of consciousness
- History of seizures or on medications that reduce seizure threshold (e.g., olanzapine, chlorpromazine, lithium)
- Neurological or uncontrolled medical disease
- Any unstable medical condition
- Active substance abuse
- Diagnosis of psychotic or bipolar disorder
- A prior history of Electroconvulsive Therapy (ECT) failure
- History of suicide attempt in the past year
- Currently pregnant or breastfeeding
- Repetitive Transcranial Magnetic Stimulation (rTMS) treatment in the past six months
Recruiting US locations
University of Iowa
Iowa City, CA 52246
Site contact: Jade T Truong, BS · 408-840-3313 · kellerlab@stanford.edu
Stanford University
Stanford, CA 94305
Site contact: Jade T Truong, BS · 408-840-3313 · kellerlab@stanford.edu
Study contacts (from the official record)
- Jade T Truong, BS · 408-840-3313 · kellerlab@stanford.edu
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