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 have a primary diagnosis of a schizophrenia-related condition or a mood disorder that includes psychotic features, as confirmed by their treatment team or medical records.
- People who have been assessed by a licensed psychologist or attending psychiatrist as being able to understand and agree to take part in the study.
- People who are experiencing sleep problems, shown either by a score of 8 or higher on a standard sleep questionnaire called the Insomnia Severity Index, or by having nightmares at least once a week.
Who may not be able to join:
- People whose psychosis is primarily caused by substance use or a medical condition.
- People who have an intellectual or developmental disability.
- People who have a condition that causes progressive loss of brain function (such as dementia).
- People who have an implanted medical device, such as a pacemaker.
- People who are currently on one-to-one supervision or 15-minute safety checks due to concerns about suicide risk or aggression.
- People whose roommate is currently on 15-minute safety checks, as this may disturb sleep during the study.
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: Alia Warner, Ph.D., The University of Texas Health Science Center, Houston
Phone: 713-486-2700
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 as assessed by coding percentage of use per night (based on duration of physiological measures collected per night divided by hours of sleep); Feasibility as assessed by percentage of nights used for the duration of the intervention.; Feasibility as assessed by a self-report satisfaction survey, Was It Worth It questionnaire
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.