Actively Recruiting

Phase Not Applicable
Age: 18Years - 25Years
All Genders
Healthy Volunteers
ID06743373

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

Led by University of Pittsburgh · Updated on 2026-04-06

180

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how cannabis use and stopping cannabis affect sleep, body clock rhythms, and sensitivity to light in young adults. The main questions focus on whether cannabis use and discontinuation change sleep drive and how they impact light sensitivity and the timing of the body's internal clock. The study compares regular cannabis users with non-users to explore these effects. Participants in the cannabis-using group will undergo a 1-week baseline period involving at-home monitoring with sleep diaries, actigraphy, and an EEG headband. They will then take part in a 4-week cannabis discontinuation protocol with support from a clinician and abstain from cannabis use. Both cannabis users and non-users will participate in two 2-night lab visits, one before and one after the discontinuation phase for cannabis users, to assess circadian phase and light sensitivity. Throughout the study, participants will complete various assessments including sleep tracking at home and detailed lab evaluations of circadian rhythms and retinal response. Researchers will measure homeostatic sleep drive, circadian photosensitivity, retinal responsivity, and circadian phase at different stages. The study lasts about five weeks for cannabis users and includes ongoing monitoring to understand changes related to cannabis use and abstinence.

CONDITIONS

Brief Title

Cannabis Effects on Sleep, Circadian Rhythms, and Light Sensitivity in Young Adults

Who Can Participate

Age: 18Years - 25Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18-25 years
  • Physically and psychiatrically healthy as determined by study assessments
  • Cannabis-Using group: Regular cannabis use defined as frequent (6-29 days/month) or daily use over the past 3 months
  • Cannabis-Using group: Willingness to discontinue cannabis use for 4 weeks
  • Control group: No cannabis use in the past 3 months and no daily or near-daily use in the past year
  • Control group: No history of alcohol or substance use disorders
  • Control group: No current sleep disorders including insomnia and delayed sleep phase disorder
  • Provision of written informed consent
Not Eligible

You will not qualify if you...

  • Significant or unstable acute or chronic medical conditions such as central nervous system disorders, cardiovascular disease, liver disease, migraine, peptic ulcer disease, inflammatory bowel disease, renal failure, arthritis, diabetes, and other endocrine disorders
  • History of seizure disorder
  • Eye or retinal conditions like diabetic retinopathy or glaucoma
  • Past or current bipolar disorder or psychotic disorders
  • Daily alcohol use or regular illicit drug use other than cannabis
  • Past or current substance use disorders excluding mild alcohol, cannabis, or nicotine use disorders
  • Syndromal sleep disorders other than insomnia and delayed sleep phase disorder, including narcolepsy, restless legs syndrome, obstructive sleep apnea, and current night shift work
  • Travel across two or more time zones in the past 60 days
  • Use of benzodiazepines or non-benzodiazepine hypnotic drugs
  • Individuals using medical marijuana for qualifying physical medical conditions other than mental health conditions
  • Unstable or uncontrolled health conditions affecting sleep, retinal function, or well-being as determined by medical history questionnaire and screening assessments

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Baseline Monitoring

Duration - 1 week

Participants complete a 1-week baseline period involving at-home sleep monitoring using sleep diaries, actigraphy, and an EEG headband.

1 week of at-home monitoring

Initial Lab Assessment

Duration - 2 nights

Participants attend a 2-night laboratory visit for circadian phase and light sensitivity assessments.

1 visit lasting 2 nights (in-person)

Cannabis Discontinuation (Cannabis Users Only)

Duration - 4 weeks

Cannabis-using participants undergo a 4-week cannabis abstinence protocol with clinician orientation and monitoring to assess effects on sleep and circadian rhythms.

Weekly visits for up to 4 weeks

Post-Discontinuation Lab Assessment (Cannabis Users Only)

Duration - 2 nights

Cannabis-using participants attend a second 2-night laboratory visit after the discontinuation period to reassess circadian phase and light sensitivity.

1 visit lasting 2 nights (in-person)

Trial Site Locations

Total: 1 location

1

Western Psychiatric Hospital (Thomas Detre Hall)

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

B

Brant P Hasler, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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