Actively Recruiting
Neuroimaging of Instrumental Learning Networks in Adolescent Cannabis Use Treatment
Led by Indiana University · Updated on 2026-05-05
80
Participants Needed
1
Research Sites
N/A
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
Researchers are studying whether brain activity related to learning can predict how well teens respond to a treatment program aimed at reducing cannabis use. This research involves adolescents aged 14 to 17 who have varying levels of cannabis use, focusing on brain function during instrumental learning and its association with cannabis use disorder symptoms and treatment success. Participants will undergo a functional magnetic resonance imaging (fMRI) scan while performing a learning task to assess brain activity. They will then take part in a 10-week virtual contingency management program, where they report cannabis use and provide weekly urine drug screens administered by their guardians. Participants can earn prizes for producing drug-free urine tests and reporting no cannabis use during the sessions. After the treatment phase, there is a follow-up visit to assess cannabis use disorder symptoms and readiness to change. Throughout the study, participants and their guardians will receive training on how to use urine drug screens at home. Questionnaires on cannabis cravings and withdrawal symptoms will be completed weekly during the virtual sessions. Researchers will measure cannabis use frequency, quantity, withdrawal, expectancy, and urine drug screen results at several points, including baseline, weekly during treatment, and post-treatment follow-up. The total study participation lasts approximately 13 weeks, including brain scans, virtual sessions, and follow-up assessments.
CONDITIONS
Brief Title
Neuroimaging of Adolescent Cannabis Use Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Youth aged 14 to 17 years
- Guardian 18 years or older
- Eligible for MRI scan (no metal implants, prosthetics, orthodontic devices, transdermal patches, removable piercings or extensions, metal tattoos on neck/face, not claustrophobic, not pregnant)
- Used cannabis at least once per week in the past month OR diagnosed with cannabis use disorder within the past three months
You will not qualify if you...
- History of Fetal Alcohol Spectrum Disorder, intellectual or developmental disorders, autism spectrum disorder, psychotic disorders, or neurological problems (e.g., epilepsy, brain injury, tumor, stroke) as reported by parent/guardian
- Monolingual non-English speaking youth or caretaker
- Currently experiencing active psychosis symptoms, suicidal or homicidal thoughts, or hospitalization for these issues within the past 6 months
- Currently receiving contingency management treatment for cannabis use disorder
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo an fMRI scan while performing an instrumental learning task and receive training on administering urine drug screens.
1 visit (in-person)
Duration - 10 weeks
Participants engage in weekly virtual contingency management sessions via telehealth to support abstinence from cannabis, submitting urine samples for drug screening and completing questionnaires about cannabis use and withdrawal symptoms.
Weekly visits for 10 weeks (virtual telehealth sessions)
Duration - 2 to 4 weeks
Participants return for an in-person visit to answer questions regarding cannabis use disorder symptoms and readiness to change after completing the treatment.
1 visit (in-person)
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
K
Katherine LeFevre, BS
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1