Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
Healthy Volunteers
NCT05336084

Circadian Rhythms and Homeostatic Sleep Drive and Their Effect on Reward and Cognitive Control Systems in Adolescents

Led by University of Pittsburgh · Updated on 2026-04-08

200

Participants Needed

1

Research Sites

430 weeks

Total Duration

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Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Institute on Drug Abuse (NIDA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Adolescence is a time of heightened reward sensitivity and greater impulsivity. On top of this, many teenagers experience chronic sleep deprivation and misalignment of their circadian rhythms due to biological shifts in their sleep/wake patterns paired with early school start times, which may increase the risk for substance use (SU). However, what impact circadian rhythm and sleep disruption either together or independently have on the neuronal circuitry that controls reward and cognition, or if there are interventions that might help to modify these disruptions is unknown. Project 1 (P1), specifically examines homeostatic and circadian characteristics as mechanisms linking habitual sleep patterns, reward and cognitive control (at subjective, behavioral, and circuit levels), and longitudinal substance use risk.

CONDITIONS

Official Title

Circadian Rhythms and Homeostatic Sleep Drive and Their Effect on Reward and Cognitive Control Systems in Adolescents

Who Can Participate

Age: 13Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 13-18 years
  • Currently enrolled in a traditional high school (except during COVID-19 school closures)
  • Physically and psychiatrically healthy
  • Provided written informed consent and assent
Not Eligible

You will not qualify if you...

  • Outside the age range of 13-18 years
  • History of alcohol, cannabis, or illicit drug use more than weekly in the past year
  • Serious medical or neurological disorders, including seizures
  • Serious psychiatric disorders like bipolar disorder or schizophrenia
  • Taking antidepressants (except SSRIs/SSNIs) or medications affecting sleep/wake function unless able to discontinue for the study
  • Sleep disorders other than insomnia or Delayed Sleep Phase Disorder
  • MRI contraindications such as metal in the body or claustrophobia
  • First degree relative with bipolar disorder
  • Frequent headaches or migraines
  • Inability to swallow pills or capsules
  • Pregnancy
  • Observed Obstructive Sleep Apnea with Apnea Hypopnea Index over 5
  • Weighing less than 80 lbs or having a BMI over 35

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Western Psychiatric Hospital

Pittsburgh, Pennsylvania, United States, 15213

Actively Recruiting

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Research Team

R

Ronette Blake, MS

CONTACT

S

Sarah Aerni

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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