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RecruitingNCT07340554ACTUpdated Jun 22, 2026

Neuroimaging of Adolescent Cannabis Use Treatment

An interventional study of Contingency Management and Elastic Net Regression in Cannabis Use, Cannabis Dependence and Cannabis Use Disorder, sponsored by Indiana University. Recruiting at 1 site in United States. Open to participants aged 14 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-06-22.

Sponsored by Indiana University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Not applicable
Ages
14 Years to 17 Years
Sex
All
01

Study summary

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.

Read the detailed description

This is a 13-week clinical trial to examine whether success during contingency management treatment for cannabis use is associated with baseline functioning of instrumental learning neuro-circuitries. The investigators propose to recruit N=80 youths ages 14-17 with varying levels of cannabis use. Following phone prescreening, participants will undergo informed consent/assent and eligibility assessment with an in-person visit. Participants who are eligible will undergo a functional magnetic resonance imaging (fMRI) scan where participants will perform an instrumental learning task during a second in-person visit. At this visit, participants and participants' guardians or most recent caregiver will be provided with ten urine drug screens. A tutorial will be provided by study staff on how to administer and read urine drug screens. After the fMRI scan, participants will undergo ten weekly virtual contingency management sessions administered via HIPAA-compliant telehealth software (e.g., Microsoft Teams). At each contingency management (CM) session, participants will be asked to provide a urine sample, and participants' guardians will be asked to administer the urine drug screen based on this sample. At each contingency management session, the timeline followback will be used to assess which days since the last session participants used cannabis at all. Finally, at each contingency management session, participants will answer brief questionnaires regarding participants' current cannabis cravings and cannabis withdrawal symptoms. For the first two sessions, participants will be able to spin a virtual wheel to win prizes (either positive affirmations or amazon gift cards in varying amounts from $5-$100) for producing a urine drug screen and answering the questions. For sessions 3-10, participants will spin the virtual wheel to win prizes after producing a urine drug screen that is negative for cannabinoids and reporting that they have not used cannabis since the last session. After the ten weekly contingency management sessions, participants will return for an in-person visit where participants will answer questions regarding their cannabis use disorder symptoms during the contingency management treatment and readiness to change. The investigators' specific aims are to identify associations between baseline Cannabis Use Disorder (CUD) symptom levels and neural activity during instrumental learning in cannabis-using adolescents (Aim 1) and Identify associations between neural activity during instrumental learning and reductions in cannabis use frequency during contingency management (Aim 2).

02

Conditions studied

  • Cannabis Use
  • Cannabis Dependence
  • Cannabis Use Disorder
  • Cannabis Abuse
  • Cannabis Intoxication
  • Cannabis Smoking
  • Cannabis Withdrawal
  • Cannabis-Related Disorder
  • Cannabis Abuse, in Remission
  • Cannabis Abuse, Episodic Use
  • Marijuana
  • Marijuana Abuse
  • Marijuana Use
  • Marijuana Smoking
  • Marijuana Dependence
  • Marijuana User
  • Marijuana-Related Disorder
  • Marijuana Use Disorder
  • Addiction
  • Addiction, Substance
  • Substance Use
  • Substance Use Disorders
  • Substance Dependence
  • Substance Abuse
  • Substance Related Problem
  • Substance Abuse Drug Chronic

Keywords

  • Cannabis
  • Marijuana
  • Addiction
03

Who can participate

Ages eligible
14 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 14-17 year old youth
  • Guardian 18 years or older
  • Youth is MRI-eligible: No metal implants, prosthetics, orthodontic devices, transdermal medication patches, piercings and/or hair or eyelash extensions that cannot easily be removed, metallic ink tattoos on the neck or face, or claustrophobia, and are not pregnant
  • Youth must endorse having used cannabis at least once per week over the past month OR youth must have been diagnosed with cannabis use disorder within the past three months

Exclusion criteria

Exclusion Criteria:

  • Youth has a history of Fetal Alcohol Spectrum Disorder, intellectual disorders, pervasive development disorder or autism spectrum disorder, psychotic disorders, history of neurological problems (epilepsy, traumatic brain injury, brain tumor, cerebrovascular disease) by parent/guardian report
  • Youth or caretaker who is monolingual non-English speaker
  • Youth who is currently experiencing active psychosis symptoms or suicidal/homicidal ideation or who has been hospitalized within the past 6 months for psychosis or suicidality/homicidality
  • Youth who is currently undergoing contingency management treatment for cannabis use disorder
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Other
    Contingency Management and Elastic Net Regression

    All participants will receive Contingency Management treatment for Cannabis Use. An elastic net regression model will be applied to the neuroimaging data for all participants to estimate scores on the CUDIT.

    Behavioral: Contingency Management · Device: Elastic Net Regression

Interventions

  • BehavioralContingency Management

    Contingency management is an evidence-based behavioral intervention used to treat substance use disorders, including cannabis use disorder (CUD). Contingency management operates on the principles of instrumental learning, where positive reinforcement is used to encourage desired behaviors, such as abstinence from cannabis. First, specific target behaviors are identified for reinforcement. In CUD, this is often abstinence from cannabis use, verified through regular urine drug screens and self-reports. If the target behavior (i.e., abstaining from cannabis for a specified time period) is achieved, then patients receive tangible rewards immediately after attaining the target behavior. These rewards are often in the form of money, vouchers, or other incentives that are meaningful to the individual. We will examine whether success during contingency management treatment for cannabis use is associated with neural activity during instrumental learning in N=80 adolescents ages 14-17.

  • DeviceElastic Net Regression

    We will apply an elastic net regression model to the neuroimaging data to estimate CUDIT score based on neuroimaging data.

05

What researchers measure

Primary outcomes

  1. Cannabis use frequency

    The investigators will measure cannabis use frequency via percent of days where cannabis was used over the past 30 days via the Timeline Followback Scale (Sobell and Sobell, 1992)

    Time frame: Screening and Post-Intervention Follow-Up Visit (2-4 weeks after last CM visit)

  2. Cannabis Use Disorder Identification Test (CUDIT) Score

    The CUDIT (Adamson et al., 2010) is a measure of cannabis use disorder symptom level. This scale is an 8-item scale that asks about cannabis use disorder symptoms over the past year and is scored on a scale of 0 (no cannabis use in the past year) to 32 (daily cannabis use, physical and psychological dependence symptoms, severe cannabis misuse). The CUDIT will be measured once at the baseline screening visit.

    Time frame: Baseline

Secondary outcomes

  1. Total quantity of cannabis use

    The investigators will measure cannabis use quantity via the Timeline Followback Scale (Sobell and Sobell, 1992). For each day participants report cannabis use on the Timeline Followback Scale, participants will be asked to estimate the number of grams of cannabis used.

    Time frame: Screening and Post-Intervention Follow-Up Visit (2-4 weeks after last CM visit)

  2. Cannabis withdrawal

    Cannabis withdrawal will be measured at 12 different time points via the Cannabis Withdrawal Scale (Milin, Manion, Dare, and Walker, 2008). The Cannabis Withdrawal Scale is a 16-item scale that evaluates cannabis withdrawal symptoms, such as sleep difficulties, nervousness, anxiety, tension, and cravings for cannabis. This scale will be administered at the scanning visit, each of the 10 contingency management visits, and at the follow-up visit.

    Time frame: Screening and Post-Intervention Follow-Up Visit (2-4 weeks after last CM visit)

  3. Cannabis expectancy

    Cannabis expectancy will be measured at 2 time points via the Marijuana Effects Expectancy Scale-Brief (Torrealday et al., 2008). The Marijuana Effects Expectancy Scale-Brief is a six item scale that measures expected effects (relaxation, reduced anxiety, cravings) of marijuana use. This scale will be administered at the scanning visit and the follow-up visit.

    Time frame: Screening and Post-Intervention Follow-Up Visit (2-4 weeks after last CM visit)

  4. Proportion of negative cannabis urine drug screen

    Urine drug screens will be collected at each visit (13 total). The investigators will track the proportion of urine drug screens that are negative over all visits and that are negative over the 10 contingency management visits.

    Time frame: Screening, Baseline, once weekly at each CM visit, and Post-Intervention Follow-Up Visit (2-4 weeks after last CM visit)

06

Study locations

1 of 1 sites recruiting
  • Indiana University School of Medicine
    Indianapolis, Indiana 46202, United States
    Recruiting
07

Registry details

Key details

Study ID
NCT07340554
Lead sponsor
Indiana University
Collaborators
National Institute on Drug Abuse (NIDA)
Responsible party
Joseph Aloi (Assistant Professor, Indiana University) — Principal investigator
First posted
Jan 14, 2026
Start date
Jun 15, 2026
Primary completion
May 1, 2030 (estimated)
Completion
May 1, 2030 (estimated)
Last update
Jun 22, 2026

Study contacts

Joseph Aloi, MD, PhD
Contact
liferaft@iu.edu
317-278-5433
Katherine LeFevre, BS
Contact
liferaft@iu.edu
317-278-5433

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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