Cannabis Effects on Sleep, Circadian Rhythms, and Light Sensitivity in Young Adults
Launched by UNIVERSITY OF PITTSBURGH · Dec 15, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring how using cannabis affects sleep and our body's internal clock, known as circadian rhythms, in young adults aged 18 to 25. Researchers want to find out if using cannabis changes how well people sleep and how sensitive they are to light, as well as the effects of stopping cannabis use for a month. The trial is currently looking for participants, including those who regularly use cannabis and healthy individuals who do not use cannabis at all.
To join the study, cannabis users must have used it frequently for the past three months and be willing to stop for four weeks. Healthy participants must not have used cannabis in the last three months and should not have any current sleep disorders or a history of substance abuse. Those interested in participating will be asked to provide consent and may need to answer questions about their health and lifestyle. Participants can expect to contribute to research that may help us understand the effects of cannabis on sleep patterns and overall well-being.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Age 18-25 years
- • Physically and psychiatrically healthy
- • 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 lifetime history of engaging in daily or near-daily cannabis use over any month-long period. 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
- 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), supplemented by clinical interview and the WHO-DAS 2.0. Researchers will not exclude participants for subsyndromal symptoms or disorders in these domains. Researchers will not exclude participants for other psychiatric disorders, particularly given the high comorbidity between cannabis use disorder and major depression and anxiety disorder, 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 and nicotine use disorder.
- • 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.). Researchers will not exclude for subsyndromal symptoms or disorders in these domains. Researchers 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 Structured Clinical Interview for Sleep Disorders, Revised Version (SCISD-R). 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/SSNIs, 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.
About University Of Pittsburgh
The University of Pittsburgh is a leading research institution known for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a robust infrastructure for research and a multidisciplinary approach, the university fosters collaboration among experts in various fields, facilitating the development of novel therapies and interventions. Its clinical trial programs emphasize ethical standards, patient safety, and the integration of cutting-edge technology, making the University of Pittsburgh a pivotal contributor to the landscape of clinical research and a trusted partner in the pursuit of health advancements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Pittsburgh, Pennsylvania, United States
Patients applied
Trial Officials
Brant P Hasler, PhD
Principal Investigator
University of Pittsburgh
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported