Actively Recruiting
Neuroimaging of Adolescent Cannabis Use Treatment
Led by Indiana University · Updated on 2026-05-05
80
Participants Needed
1
Research Sites
204 weeks
Total Duration
On this page
Sponsors
I
Indiana University
Lead Sponsor
N
National Institute on Drug Abuse (NIDA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is testing whether brain activity related to learning can help predict how well teens respond to a treatment program designed to reduce cannabis use. Teens ages 14-17 will complete a brain scan and then take part in 10 weekly virtual sessions where they report cannabis use and complete drug tests at home. Participants can earn prizes for staying cannabis-free.
CONDITIONS
Official Title
Neuroimaging of Adolescent Cannabis Use Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Youth aged 14 to 17 years
- Guardian aged 18 years or older
- Youth must be eligible for MRI (no metal implants, prosthetics, orthodontic devices, certain piercings or tattoos, not claustrophobic, and not pregnant)
- Youth must have used cannabis at least once per week in the past month or have been diagnosed with cannabis use disorder within the past three months
You will not qualify if you...
- History of Fetal Alcohol Spectrum Disorder, intellectual disorders, pervasive developmental disorder or autism spectrum disorder, psychotic disorders, or neurological problems such as epilepsy, traumatic brain injury, brain tumor, or cerebrovascular disease
- Youth or guardian is monolingual non-English speaker
- Currently experiencing active psychosis symptoms, suicidal or homicidal thoughts, or hospitalization for these within the past 6 months
- Currently undergoing contingency management treatment for cannabis use disorder
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Indiana University School of Medicine
Indianapolis, Indiana, United States, 46202
Actively Recruiting
Research Team
J
Joseph Aloi, MD, PhD
CONTACT
K
Katherine LeFevre, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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