Depression and Anxiety Trial, Recruiting NCT07217223 Sponsor: University of California, San Diego Condition: Depression and Anxiety
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Depression and Anxiety Trial, Recruiting

NCT07217223
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 18 and 85 years old at the time of screening
  • People who have been diagnosed with Major Depressive Disorder (MDD) and have a symptom score of 20 or higher on a standard depression scale called the MADRS
  • People who have been assessed as safe to receive a brain stimulation treatment called TMS, based on a standard safety screening tool
  • People whose medical records show that at least one adequate antidepressant medication trial did not work well enough, or that at least two lower-dose antidepressant trials were not tolerated, based on a scoring tool called the ATHF (confirm with trial site)
  • People who have a stable internet connection and a device that works with Microsoft Teams

Who may not be able to join:

  • People with a history of psychotic disorders, bipolar disorder, or depression with psychotic features
  • People with significant borderline personality disorder
  • People with significant obsessive-compulsive disorder or post-traumatic stress disorder
  • People currently experiencing a moderate or severe substance use disorder, or showing signs of acute substance withdrawal
  • People with clinically significant concerns around suicidality
  • People whose depression has lasted continuously for more than 5 years
  • People who are pregnant or breastfeeding, or women of childbearing age who do not have adequate contraception in place
  • People with a significant neurological condition, such as dementia, Parkinson's disease, Huntington's disease, a brain tumour, seizure disorder, bleeding around the brain, multiple sclerosis, or a history of serious head injury with ongoing symptoms
  • People with an unstable medical condition
  • People for whom a brain stimulation treatment called tDCS would be medically unsafe — for example, those with certain metal implants, a history of seizures, or a known brain lesion
  • People who have previously had more than 15 TMS sessions without meaningful improvement, or more than 4 ketamine sessions without meaningful improvement
  • People who require a benzodiazepine medication at a dose higher than the equivalent of 2 mg per day of lorazepam
  • People with skin conditions that would make tDCS unsafe to use
  • People with sensory impairments that cannot be corrected
  • People who are unable to give informed consent or who are unable to participate in the trial as an outpatient

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 858-966-5832

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
27 September 2025
Est. completion
1 October 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Feasibility (Recruitment); Feasibility (Retention); Feasibility (Adherence); Safety of at-home spaced tDCS; Tolerability to spaced tDCS

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov