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:
- People who can read and understand study materials written in English, confirmed by a standard reading test score above 85
- People who score 18 or higher on a depression symptom questionnaire (called the MADRS-S) during the screening process
- People who have been diagnosed with Major Depressive Disorder (a serious form of depression) confirmed by a clinician interview
- People who are taking antidepressant medication only if their dose has stayed the same for at least 30 days before the screening period
- People who have either a local doctor or healthcare provider responsible for their ongoing care and available to be contacted if needed, or who have confirmed knowledge of local support resources
- People who are able to give informed consent and follow the study procedures
- People who have access to a quiet space at home suitable for brain stimulation sessions
Who may not be able to join:
- People with a significant ongoing medical condition that, in the opinion of the study clinician, could interfere with participation, safety, or the study results
- People with a current or past diagnosis of bipolar disorder or a psychotic disorder, or who have had an alcohol or substance use disorder in the past 6 months, as determined during the screening interview
- People with serious thoughts of suicide or suicidal behaviour, based on clinician assessment and a formal rating scale
- People who have used prescription or over-the-counter sleep medications, or started a sleep-focused therapy programme, in the 30 days before screening
- People with a history of seizures or epilepsy
- People who have an active implanted medical device located above the neck (such as a deep brain stimulator or cochlear implant), or metal implants in the head or neck area that are not compatible with MRI
- People who are currently using any prescription or over-the-counter sleep medications, or are actively taking part in any treatment specifically aimed at improving sleep
- People who are currently pregnant, planning to become pregnant during the study, or who are breastfeeding — people who could become pregnant would be required to use an accepted form of contraception throughout the study (confirm with trial site for full details)
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: Giuseppina Pilloni, NYU Langone Health
Phone: 929-455-5104
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 sleep efficiency
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.