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 score 48 or higher on a standard questionnaire measuring sleep disturbance (called the PROMIS sleep disturbance short form)
- People who score 55 or higher on a standard questionnaire measuring anxiety or depression (called the PROMIS anxiety or depression short form), which corresponds to at least mild symptoms
Who may not be able to join:
- People who are currently taking antidepressants, anti-anxiety medications, or sleep aids, including melatonin
- People who are currently pregnant
- People who have allergies or sensitivities to scented lotion
- People who are not able or willing to keep a roughly consistent bedtime (within about one hour) throughout the treatment weeks of the trial
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: Lisa E Olson, Ph.D., University of Redlands
Phone: 909-748-8524
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
Sleep disturbance; Anxiety; Depression; Total sleep time; Sleep efficiency; Normalized high frequency power of heart rate variability; Anxiety by momentary ecological assessment; Mood by momentary ecological assessment; Salivary alpha-amylase
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.