The purpose of the study is to evaluate whether Lemborexant is more effective than placebo in shortening sleep onset latency in patients with delayed sleep phase syndrome (both type 1 and type 2). This will be tracked using sleep logs as well as actigraphy. In this 2-year study, the investigators will examine if Lemborexant administered 5-10 mg nightly taken at desired bedtime (at least 2 hours prior to self-reported sleep onset habitual time) can improve the symptoms of Delayed Sleep Phase Syndrome.
Delayed sleep phase syndrome (DSPS) is a disorder in which a person's sleep is delayed by two hours or more beyond what is considered an acceptable or conventional bedtime. The delayed sleep then causes difficulty in being able to wake up at the desired time. In DSPS, bedtime is shifted later than the general population such that individuals have difficulty getting enough sleep to meet their sleep need before they have to get up for their daytime obligations (work, school, childcare, etc.). As a result, patients experience daytime impairment including daytime sleepiness and cognitive impairment. DSPS, if maintained in adulthood is associated with numerous deleterious health effects, although causality is not well established. The prevalence of this condition is approximately 7-16% among adolescents and young adults.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
15
Lemborexant tablet administered orally once daily
Placebo to match Lemborexant tablet administered orally once daily
University of California San Francisco
San Francisco, California, United States
RECRUITINGChange in actigraphy sleep latency onset
Sleep latency is the time from laying down until falling asleep. Actigraphy data obtained using Axivity- AX6.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Change in Epworth Sleepiness Scale (ESS)
This is a scale to evaluate daytime sleepiness. Range from 0 to 24 points (higher scores mean more sleepiness).
Time frame: From randomization to 4 weeks post randomization
Change in Karolinska Sleepiness Scale (KSS)
Self-report for daytime sleepiness with 1 being extremely alert and 10 being extremely sleepy, can't keep awake.
Time frame: From randomization to 4 weeks post randomization
Change in sleep diary derived sleep onset latency
Sleep latency is the time from laying down until falling asleep as estimated by patient in dairy.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Sleep Regularity Index
Sleep Regularity Index is defined as the percentage probability of a person being asleep (or awake) at any two time points 24 hours apart. Actigraphy data obtained using Axivity- AX6.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Change in actigraphy derived total sleep time
Actigraphy data obtained using Axivity- AX6.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Change in sleep diary derived total sleep time.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Estimated by patient in dairy.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Change in mean actigraphy derived wake time
Wake time is total time awake over night after sleep onset. Actigraphy data obtained using Axivity- AX6.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization
Change in mean sleep diary derived wake time
Wake time is total time awake over night after sleep onset as estimated by patient in dairy.
Time frame: From 2 weeks prior to randomization to 4 weeks post randomization