tDCS for Mild to Moderate Depression

Heart Rate Variability (HRV)-Guided Transcranial Direct Current Stimulation (tDCS)

Recruiting N/A Interventional Study
Depression
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
100 (estimated)
Sponsor
NYU Langone Health · Other
Who this trial is looking for

This trial is looking for people with mild to moderate depression. Participants will receive a type of brain stimulation called tDCS for 30 minutes each day for 10 days while their heart activity is monitored.

Are You a Good Fit for This Trial?
Must not be taking Beta-blockersCalcium channel blockersCardiac glycosidesAntidepressantsAntipsychoticsAnxiolytics
Rules you out Bipolar depressionPsychotic disorderAlcohol use disorderSubstance use disorder

You may be able to join if

  • I have mild to moderate depression.
  • I have a score of 14-28 on the Beck Depression Inventory.
  • I have been diagnosed with a depressive episode.

You may not be able to join if

  • I have a serious neurological or psychiatric condition.
  • I have a history of suicide risk.
  • I have a heart condition or a history of heart transplant.
  • I am pregnant or planning to become pregnant.
  • I have had seizures in the last 5 years.
  • I have any metal objects in my head or neck.
  • I have a skin disorder near the stimulation area.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial
This technology development project will be informed and guided by initial data collection of human subject data. For this purpose, the investigators will recruit n=100 people with mild to moderate depression in a double-blinded, parallel-arm, sham-controlled data collection period administered at home and using the investigator's remotely supervised (RS) tDCS protocol. Enrolled participants will …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Mild to moderate depression (Beck Depression Inventory(BDI)-II 14-28) * Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-V-TR) Depressive episode * Wide Range Achievement Test (WRAT)-4th Reading Recognition subtest standard score \>85 E…
Contacts

Shayna Pehel

929-455-5104

Shayna.Pehel@nyulangone.org

CONTACT