Depression and Anxiety Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Feasibility (Recruitment); Feasibility (Retention); Feasibility (Adherence); Safety of at-home spaced tDCS; Tolerability to spaced tDCS
Can't join this trial?
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.