Targeting depression: can MRI-Guided brain zaps rewire key circuits?
NCT ID NCT05090397
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This study tests whether a mild electrical brain stimulation technique called transcranial direct current stimulation (tDCS) can alter brain activity in adults with major depression. Using MRI to guide the stimulation, researchers will measure changes in brain connectivity and also track depressive symptoms over five sessions. The goal is to understand how tDCS affects the brain, not yet to prove it as a treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcranial direct current stimulation (tDCS), a mild electrical current applied to the scalp, guided by MRI
- What this could lead to
- If it works, this could point toward a more targeted, personalized way to use brain stimulation for depression.
- What could go wrong
- This is a small, early-stage study focused on brain changes, not proof of treatment benefit. Results may not translate into lasting symptom relief.
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
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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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26 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Mar 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 65 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: * 1\. Ages between 18 and 65 * 2\. Race/ethnicity: all races and ethnic groups * 3\. Sex/Gender: all * 4\. Capacity to provide informed consent * 5\. Diagnosis of Major Depressive Disorder made by volunteer's physician at least one year prior (confirmed by patient self-report) * 6\. Currently under the care of a clinician for depression (psychiatrist, psychologist, or other clinician) * 7\. Currently experiencing symptoms of depression (Patient Health Questionnaire 9, PHQ9 \>4 at screening; Hamilton Depression Rating Scale 17-item, HDRS-17, score \>8 at Visit 1) * 8\. Stable or no pharmacological antidepressant regimen (SSRI, SNRI, MOAI, or tricyclic/TCA) with no change in treatment 6 weeks prior to study start Exclusion Criteria: * 1\. Ages below 18 (neurobiology is quite different in children vs. adults) * 2\. Ages above 65 (cortical excitability changes with age) * 3\. Active suicidal thoughts, ideation, or behavior with plan within the past month (HDRS-17 item 3 score 3-4) * 4\. Change in antidepressant medication within 6 weeks of study start * 5\. Diagnosis of any medical condition potentially affecting brain function: neuropsychiatric or mental disorders, other mood disorders (bipolar disorder, primary anxiety disorder, PTSD), psychotic states or disorders, developmental disorders, neurological disorders, including mild cognitive impairment, significant head injury, significant history of alcohol/substance abuse or dependence within past 12 months, chronic pain (current, or for more than one year within the past one year), other major medical conditions (e.g., cancer, stroke). * 6\. MRI contraindications: metal or other implants that are not MR-safe, claustrophobia, pregnancy or suspected pregnancy * 7\. tES contraindications: skin conditions or injuries on the scalp hair extensions, wigs, braids, etc. that cannot be removed prior to the study, metal implants or pacemakers (also contraindicated for MRI) * 8\. Non-English speakers (due to written consent and questionnaires administered) * 9\. Neurostimulation or neuromodulation treatment for any reason within the past 3 months * 10\. Current medication use potentially affecting brain function, including decongestants, antihistamines, benzodiazepines or other anticonvulsants, anti-psychotics. * 11\. Prisoners will not participate in this 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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CTI Northwestern
Chicago, Illinois, 60611, United States
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Other studies related to the condition(s) this trial covers.
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