Clinical trial Recruiting at 1 site Interventional Ages 18 to 25

Effects of cannabis on sleep and light sensitivity in young adults

Official title: Cannabis Effects on Sleep, Circadian Rhythms, and Light Sensitivity in Young Adults (CASCILS)

Run by University of Pittsburgh · NCT06743373 · Data updated 2026-11-12

This study tests how using and stopping cannabis affects sleep and light sensitivity in young adults aged 18 to 25.

More Cannabis Use trials

Quick facts

Study typeInterventional
Ages18 Years to 25 Years
SexAll
Enrollment180 (estimated)
SponsorUniversity of Pittsburgh
Academic / other
Locations1 site (Pittsburgh, Pennsylvania)
StatusRecruiting
StartedMarch 13, 2025
Main results expectedJanuary 31, 2029
Study endsApril 30, 2029
Registry record updatedApril 6, 2026
Trial IDNCT06743373 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are healthy young adults aged 18-25 who are regular cannabis users or non-cannabis users without a history of substance use disorders.

Probably not a fit

Patients with significant medical conditions or current sleep disorders may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates how cannabis use and its discontinuation influence sleep patterns, circadian rhythms, and sensitivity to light in young adults aged 18-25. Participants will undergo a one-week baseline monitoring period, followed by a two-night lab assessment of their circadian phase and light sensitivity. Regular cannabis users will then participate in a four-week cannabis discontinuation protocol, after which they will return for a second lab visit to evaluate changes. The study also includes a control group of non-cannabis users for comparative analysis.

Why it matters

Potential benefit: If successful, this study could provide insights into the effects of cannabis on sleep and circadian rhythms, potentially guiding treatment for sleep disorders.

How similar studies have gone: While there have been studies on cannabis and sleep, this specific approach focusing on light sensitivity and circadian rhythms in young adults is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
List the inclusion criteria:

* Age 18-25 years
* Physically and psychiatrically healthy, as determined by instruments described below
* Cannabis-Using group only: Regular cannabis use, defined as "frequent" (6-29 days/month) or "daily" (daily) use over the past 3 months
* Cannabis-Using group only: Willingness to discontinue cannabis for 4 weeks.
* Control group only: No cannabis use in the past 3 months. Deny engaging in daily or near-daily cannabis use during the past year. No history of alcohol and/or substance use disorders. No current sleep disorders (including insomnia and delayed sleep phase disorder).
* Provision of written informed consent

List the exclusion criteria:

* Significant or unstable acute or chronic medical conditions. Examples of such conditions include, but are not limited to, central nervous system disorders (e.g., head injury, seizure disorder, multiple sclerosis, tumor), cardiovascular or hemodynamically significant cardiac disease, liver disease (e.g., acute or chronic hepatitis, hepatic insufficiency), migraine or chronic headaches, active peptic ulcer disease, inflammatory bowel disease, renal failure, arthritis, and diabetes and other endocrine disorders. Seizure disorder in particular will be exclusionary due to the increased risk it confers for cannabis withdrawal symptoms. Eye/retinal conditions such as diabetic retinopathy or glaucoma will be exclusionary, although should be very rare in this population. Individuals with well-controlled health conditions that do not affect sleep, retinal function, and/or well-being (e.g., well-controlled thyroid disorders, asthma, or ulcer) will not be excluded. To evaluate these criteria, potential participants will complete a locally-developed Medical History Questionnaire.
* Past or current DSM-5 bipolar disorder or psychotic disorders. Psychiatric disorders will be evaluated using the Mini International Neuropsychiatric Interview (MINI) and the WHO-DAS 2.0, supplemented by clinical interview. We will not exclude participants for subsyndromal symptoms or disorders in these domains. We will not exclude participants for other psychiatric disorders, particularly given the high comorbidity between cannabis use disorder and major depression and anxiety disorder, as long as severity is in the moderate range or lower based on the WHO-DAS 2.0 (average score \<4).
* Daily use of alcohol; regular use of illicit substances. Regular use (as defined above) of illicit substances other than cannabis over the past 3 months will be exclusionary. Substance use will be assessed using the Timeline Follow Back method, as well as a urine drug screen.
* Past or current substance use disorders other than cannabis use disorder, nicotine use disorder, and mild alcohol use disorder (moderate and severe alcohol use disorder are exclusionary).
* Current syndromal sleep disorders other than insomnia and delayed sleep phase disorder, including narcolepsy, restless legs syndrome, obstructive sleep apnea, and current night shift work (i.e., any work occurring between the hours of midnight and 6:00 a.m.). We will not exclude for subsyndromal symptoms or disorders in these domains. We will not exclude Cannabis-using participants for insomnia and delayed sleep phase disorder because of their conceptual overlap and high co-occurrence with sleep phenotypes of interest. Sleep disorders will be diagnosed according to criteria in the DSM-5 and the International Classification of Sleep Disorders, 3rd Edition, 2014. These disorders will be evaluated using clinical interview and the locally-developed Structured Clinical Interview for Sleep Disorders. Control participants will be excluded for any current sleep disorders, including insomnia and delayed sleep phase disorder.
* Travel across 2+ time zones in the past 60 days.
* Benzodiazepines and non-benzodiazepine hypnotic drugs ("Z-drugs"). Other sleep-promoting medications will be permitted, including SSRIs/SNRIs, will be permitted if on stable dose and not in the acute phase of treatment. In order to evaluate medications, participants will complete a listing of current medications, including prescription and over the counter medications, "natural" preparations, and nutritional supplements.
* Individuals with a Pennsylvania Medical Marijuana Card using dispensary-obtained marijuana or other THC products for documented Qualifying Medical Conditions other than those of a mental health nature will be excluded. However, individuals who have been issued a Pennsylvania Medical Marijuana ID card for a mental health condition will not be excluded from the study.

There will not be any Medical Record review. For most individuals, the Medical History Questionnaire, including medical conditions and medications, will be sufficient for identifying exclusionary medical criteria. For instances where an individual is uncertain about exclusionary or current medical conditions or medications, medical records, prescription records or labeled prescription pill bottles, or a Release of Information to contact the individual's Primary Care Practitioner \[PCP\] to clarify the individual's medical status will be obtained.

Where it's running

  • Western Psychiatric Hospital (Thomas Detre Hall)
    Pittsburgh, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Brant P Hasler, PhD — University of Pittsburgh
  • Study coordinator: Brant P Hasler, PhD
  • Email: haslerbp@upmc.edu
  • Phone: 412-246-6413

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.