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Characterization of Endocannabinoid and Endogenous Opioid Levels in Adolescents With Cannabis Use Disorder

Characterization of Endocannabinoid and Endogenous Opioid Levels in Adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05396638
Enrollment
30
Registered
2022-05-31
Start date
2022-10-13
Completion date
2026-12-01
Last updated
2026-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cannabis Use

Brief summary

This project seeks to learn more about the effects of cannabis use on the endocannabinoid system and endogenous opioid systems in adolescents to address a fundamental gap in knowledge and identify biomarkers that may help distinguish youth who relapse from youth who remain sober.

Detailed description

Learning the effects of cannabis use on the endocannabinoid system and endogenous opioid systems in adolescents addresses a fundamental gap in knowledge and may identify biomarkers that help distinguish youth who relapse from youth who remain sober. The specific aims of the project are to: 1. Measure endocannabinoid (eCB) and endogenous opioid (endorphin) levels in the blood of adolescents who use cannabis regularly and adolescents who never use cannabis. We expect eCB and endorphin levels to differ significantly in adolescents who use cannabis regularly compared to adolescents who do not. 2. Characterize circulating eCB and endorphin levels at baseline, during abstinence, and after natural resumption of cannabis use. 3. Collect data to evaluate cannabis craving and to test for association of craving with eCB and endorphin levels in adolescents who use cannabis regularly. We expect that larger changes in eCB and endorphin levels will be associated with higher craving scores.

Interventions

BEHAVIORALContingency Management

Participants will be paid for abstinence at each study visit.

Sponsors

University of Colorado, Denver
Lead SponsorOTHER
Colorado Clinical & Translational Sciences Institute
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

The contingency management (CM) procedure will consist of a four-week abstinence-based incentive program. At the initial visit, participants will be instructed to refrain from using cannabis for the next month and abstinence will be monitored by urine and saliva drug tests. Participants will be paid at each study visit for attendance and abstinence. CM payment rates for abstinence will revert to the initial payment level following a missed study visit or if THC levels rise or are detected by saliva drug screen, respectively.

Eligibility

Sex/Gender
ALL
Age
14 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

1. 14 to 25 years of age. 2. Use cannabis at least twice a week for the past month.

Exclusion criteria

1. Refusal of valid written consent, 2. Current psychosis, 3. Obvious intoxication, 4. Current risk of suicide, 5. Violence sufficiently great to interfere with evaluation or to endanger evaluators, 6. Obvious intellectual deficiency as noted during the informed consent process, or inability of patient or family to comply with the study protocol. 7. Use of other illicit drugs in the past 90 days by self-report or detected by urine drug test. 8. Use of opioid medications for medical or recreational purposes currently or within the past 90 days. 9. Does not have access to an Internet connected devise or cannot use Zoom.

Design outcomes

Primary

MeasureTime frameDescription
Cannabinoid levels in bloodCollected at BaselineCannabinoid levels in blood: Our primary measure will be 11-nor-carboxy-Δ9-tetrahydrocannabinol (THCCOOH) concentrations in whole blood, which have been demonstrated to be a reliable quantitative measure of cannabis use over the past few weeks35. We will measure an additional 10 cannabinoids \[THC, 11-hydroxy-THC, THC-glucuronide, cannabidiol (CBD), cannabinol (CBN), cannabigerol (CBG), cannabichromene (CBC), cannabidivarin (CBDV), tetrahydro-cannabivarin (THCV), and THCV-COOH\]34, which will be visually inspected to identify potential secondary outcomes.
Endocannabinoid levels in bloodCollected at BaselineWe will measure endocannabinoid (eCB) levels AEA and 2-AG, the primary eCBs, in whole blood.

Secondary

MeasureTime frameDescription
Endorphin levels in bloodCollected at BaselineEndorphin levels in blood: Circulating beta Endorphin (b-EP) levels will be quantified using a commercially available enzyme-linked immunosorbent assay (ELISA) kit.
Cannabis CravingCollected at BaselineCannabis craving: The Marijuana Craving Questionnaire (MCQ) will be used to assess cannabis craving.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026