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NCT03556124 · ClinicalTrials.gov registry record · NA

Transcranial Direct Current Stimulation in Major Depression

A NA study of Major Depressive Disorder, sponsored by University of California, Los Angeles.

Completed
Registry status
NA
Development phase
66
Enrollment target
1
Study location

NCT03556124: Completed NA study of Major Depressive Disorder, sponsored by University of California, Los Angeles.

NCT03556124 is a NA study of Major Depressive Disorder that has completed, run by University of California, Los Angeles. The registered enrollment target is 66 participants, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03556124, a NA study of Major Depressive Disorder, has completed, sponsored by University of California, Los Angeles.

COMPLETED
Registry status
NA
Development phase
66 participants
Enrollment target
1
Study location

Study Summary

Noninvasive transcranial direct current stimulation (tDCS) is a low-intensity neuromodulation technique of minimal risk that has been used as an experimental procedure for reducing depressive symptoms and symptoms of other brain disorders. Though tDCS applied to prefrontal brain areas is shown to reduce symptoms in some people with major depressive disorder (MDD), the extent of antidepressant response often differs. Methods that map current flow directly in the brain while a person is receiving tDCS and that determine how functional neuroimaging signal changes after a series of tDCS sessions may help us understand how tDCS works, how it can be optimized, and if it can be used as an effective intervention for reducing depressive symptoms. We will investigate these questions in a two-part randomized double blind exploratory clinical trial. The first part of the trial will compare how current flow and functional imaging signal differs in the brain when using tDCS with more focal stimulation, called high definition (HD) tDCS, compared to conventional tDCS (C-tDCS) or sham (non-active) tDCS in patients with MDD. Sixty people with depression (20 in each group) will be randomized to receive either HD-tDCS, C-tDCS or sham-tDCS for a total of 12 sessions each lasting 20 minutes occurring on consecutive weekdays. At the first and last session, subjects will receive 20-30 minutes of active or sham tDCS in the MRI scanner, which will allow us to map tDCS currents, and track changes in regional cerebral blood flow (rCBF) pre-to- post treatment using completely non-invasive methods. At the first and last session and mid-way through the trial, participants will also complete a series of clinical ratings and neurocognitive tests

Primary Outcome

Modulation of the left dorsolateral prefrontal cortex (DLPFC) and dorsal anterior cingulate cortex (dACC) measured by percent rCBF signal change

Conditions Studied

Interventions

  • DEVICE Active - HD tDCS
  • DEVICE Sham - HD tDCS
  • DEVICE Active - Conventional tDCS
  • DEVICE Sham - Conventional tDCS

Study Locations (1)

California

  • University of California, Los Angeles (UCLA) - Los Angeles

Trial Details

FieldValue
Enrollment Target 66 participants
Start Date 2018-02-02
Est. Completion 2020-05-31
Phase NA

What the finished NCT03556124 record still lists

NCT03556124 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 66 participants, a relatively small participant target, below the 377-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (82% lower).

The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 4 interventions - of which Active - HD tDCS is the first listed.

NCT03556124 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT03556124 about?

NCT03556124 is a clinical study titled "Transcranial Direct Current Stimulation in Major Depression". Noninvasive transcranial direct current stimulation (tDCS) is a low-intensity neuromodulation technique of minimal risk that has been used as an experimental procedure for reducing depressive symptoms and symptoms of other brain disorders. Though tDCS applied to prefrontal brain areas is shown to re...

What is the current status of trial NCT03556124?

This trial is currently completed. It is a NA study. The enrollment target is 66 participants. The study started on 2018-02-02. Estimated completion is 2020-05-31.

What conditions does trial NCT03556124 study?

This clinical trial studies the following conditions: Major Depressive Disorder.

What interventions are being tested in trial NCT03556124?

The interventions under investigation include: Active - HD tDCS (DEVICE), Sham - HD tDCS (DEVICE), Active - Conventional tDCS (DEVICE), Sham - Conventional tDCS (DEVICE).

Who is sponsoring clinical trial NCT03556124?

This trial is sponsored by University of California, Los Angeles, which has 897 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03556124 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Major Depressive Disorder

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03556124's enrollment target sits among peer trials

66 162nd of 282 higher than 121 of 282 other Major Depressive Disorder trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Major Depressive Disorder trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03556124, the US trial registry maintained by the National Library of Medicine. NCT03556124 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.