Sleep Disorders 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:
- Adults between 18 and 65 years old
- People who have been diagnosed with Major Depressive Disorder (a medical diagnosis of serious, ongoing depression)
- People whose depression is currently rated as moderate to severe
- People who have tried at least one antidepressant medication in the past that did not work well enough
- People who have been on a stable, unchanged antidepressant dose for at least 6 weeks before joining the trial
- Healthy volunteers between 18 and 65 years old who do not have depression symptoms, are not taking antidepressants or antipsychotic medications, and do not have major psychiatric, neurological, substance use, or other conditions affecting brain function, may also be eligible to participate as a comparison group (confirm with trial site)
Who may not be able to join:
- People with an intellectual disability
- People with a significant head injury or a neurological disorder (a condition affecting the brain or nervous system)
- People who are pregnant or in the postpartum period (recently given birth)
- People who have any medical reasons that make TMS (a type of brain stimulation) or MRI (a type of brain scan) unsafe for them — for example, certain metal implants
- People who are currently experiencing active substance use issues or thoughts of suicide
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
Principal Investigator: Umair Hassan, PhD, Stanford University
Phone: 408-909-2203
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 Baseline TMS-EEG after iTBS; Change in Baseline TMS-EEG after NREM Sleep; Change in N-back Accuracy Performance; Change in N-back Reaction Time Performance; Change in MSIT Accuracy Performance; Change in MSIT Reaction Time Performance
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.