Phase 2 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 who have been diagnosed with a major depressive episode as part of unipolar major depressive disorder, according to standard diagnostic guidelines (DSM-5).
- People whose depression has not improved after at least one antidepressant medication trial that meets a specific level of adequacy, as measured by a clinical assessment tool called the ATHF-SF (confirm with trial site).
- People whose depression is rated as moderate to severe, based on a score above 19 on a standard depression rating scale called the MADRS.
- People who have not started a new antidepressant or increased their current antidepressant dose in the four weeks before the screening visit.
- People who are able to understand the trial and give their informed consent to participate.
Who may not be able to join:
- People who are unable to give informed consent.
- People who have a medical condition that is currently unstable.
- People who have a neurological condition, or a personal history of seizures or epilepsy.
- People who are currently showing suicidal behaviour, as measured by a clinical assessment tool called the Columbia Suicide Severity Rating Scale.
- People who are pregnant or breastfeeding.
- People who have any psychotic disorder, or who are currently experiencing psychotic symptoms.
- People who have metal implants in the skull or brain, or any other medical device or condition that the trial site considers unsafe for TMS (a type of brain stimulation treatment used in this trial).
- People for whom MRI scanning is not considered safe or suitable.
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: 858-232-2855
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
Change in EEG source localized pDMN alpha activity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.