NCT05598034Recruiting
Evaluating tDCS Brain-stimulation in Depression Using MRI
Optimization of tDCS Brain Network Engagement in Depression
Source: ClinicalTrials.gov · Last updated 8 Jun 2026
Brief summary (registry, in English)
Patients, physicians, and those who fund depression research are keenly interested in depression treatments that do not involve taking medications. One promising candidate treatment is transcranial direct current stimulation (tDCS), a low-cost technique that involves placing electrodes on specific scalp locations and using a 9-volt battery to cause a small amount of electricity to pass through parts of the brain. Depending on the direction of electrical flow, tDCS can make brain cells (neurons) more likely or less likely to generate their own electrical signals. When evaluated as a treatment, tDCS is typically done in daily sessions over a period of two weeks. One of the challenges of tDCS is to work out the best possible positioning of electrodes and direction of electricity flow to gradually cause lasting changes in brain activity in ways that might be expected to improve depression. To address this challenge, the investigators are using MRI to take pictures of the brain during tDCS. This data will help us better understand the short-term effects of tDCS in depression and help us learn how to customize future treatments to cause a lasting beneficial response. Patients with depression between the ages of 20-55 years are eligible to take part in this research. Potential participants will undergo: 1. An assessment to confirm eligibility. This will take place over a secure videoconference call lasting no more than 3 hours. 2. Two in-person study visits lasting 30 min and 2-1/2 hours respectively. In the first visit, the investigators will use the MRI to take a picture of the brain and head structure to determine appropriate locations for placing the tDCS electrodes at the start of the second visit. Following electrode placement, an MRI scan will be performed to take pictures of the brain during tDCS. Depending on the study arm, 1. Participants may receive 'active' or 'sham' tDCS. The 'sham' condition is identical to the 'active' tDCS in every way except that it involves minimal tDCS and is designed to help rule out effects unrelated to the administered tDCS electricity. 2. Participants may also be asked to perform a mental task during MRI.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 144 (estimated)
- First submitted
- 21 Oct 2022
- Start date
- 20 Oct 2022
- Primary completion date
- 1 Apr 2028
- Lead sponsor
- University of California, Los Angeles
- Diseases
- Depression
- NCT number
- NCT05598034
What you commit to
- Study type: Interventional
- Planned participants: 144
- From 20 Oct 2022 to the primary completion date, 1 Apr 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Currently receiving any form of psychotherapy
- Change in antidepressant medication within 6-weeks of starting the trial
- Any neuromodulation therapy (e.g., ECT, rTMS, DBS, VNS or tDCS) within the last 3-months
- Current use of decongestants or other medication previously shown to interfere with cortical excitability
- On regular benzodiazepine medication that it is not clinically appropriate to discontinue for the 2-week duration of the trial
Other illness
- Substance Use Disorder within last 12 months
- Neurological condition associated with brain abnormalities (e.g., traumatic brain injury; recent stroke, tumor)
- Any contraindication to tDCS (e.g., skin disease or treatment causing irritation)
- Any condition that would contraindicate scanning (metal implants, claustrophobia or a breathing or movement disorder)
- Severe or treatment resistant depression - HAMD scores \> 24 and a history of a major depressive episode lasting \>2- years or failure to 2 or more antidepressant trials in the current index episode
- Diagnosis: Schizophrenia Axis I disorder, or dementia of any type
- Bipolar I disorder (due to possible risk of mania and because lithium and anticonvulsants are excluded).
- Depression related to serious medical illness (i.e., mood disorder due to general medical condition) 17. Actively suicidal as defined by a score of 4 on item 3 of HAMD
Other
- Pregnancy
- Non-English speaking (due to scales administered)
- Current or past (within the last 1-month) use of anticonvulsants, lithium, psychostimulant, dexamphetamine
Who the study is looking for
- Age between 20 to 55 years, inclusive
- Gender: all
- Race/ethnicity: all races and ethnic groups
- Capacity to provide informed consent
- Hamilton Rating Scale for Depression score of ≥17 and \<24, with or without symptoms of anxiety.
- Treatment naïve or on a stable standard antidepressant regimen (including selective serotonin reuptake inhibitors (SSRIs), serotonin-noradrenaline reuptake inhibitors (SNRIs), monoamine oxidase inhibitors (MOAIs) or tricyclic's (TCAs)) with no change in treatment 6-weeks prior to and during the tDCS intervention.
- Work at UCLA or live within 1-hr driving distance of UCLA
Age in the registry: 20 years to 55 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of California Los Angeles (UCLA). Coordinator of this site? Confirm its status | Los Angeles | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.