Impact of Reduced Cannabis Use on Functional Outcomes
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ClinicalTrials.gov Identifier: NCT03681353 |
Recruitment Status :
Completed
First Posted : September 24, 2018
Last Update Posted : November 5, 2020
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Condition or disease | Intervention/treatment | Phase |
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Cannabis Cannabis Use | Behavioral: Mobile Contingency Management, active | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 36 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Other |
Official Title: | Impact of Reduced Cannabis Use on Functional Outcomes |
Actual Study Start Date : | April 4, 2019 |
Actual Primary Completion Date : | September 23, 2020 |
Actual Study Completion Date : | September 23, 2020 |
Arm | Intervention/treatment |
---|---|
Experimental: Reduced Use Condition
This arm includes six weeks of mobile contingency management treatment administered via a smart-phone based application (mobile CM), in which participants are provided monetary reinforcement for reducing cannabis use.
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Behavioral: Mobile Contingency Management, active
Participants are provided monetary reinforcement for providing oral fluid test results that suggest they have reduced cannabis use. |
- Number of participants who complete the baseline assessment [ Time Frame: Baseline ]Adherence is defined as completing the baseline assessment
- Number of participants who complete the 8-week follow-up assessment [ Time Frame: 8- week follow up ]Adherence is defined as completing the 8-week follow-up assessment
- Number of participants who complete 1 or more Ecological Momentary Assessments (EMA) per day (total ≥56) for the duration of the 8-week EMA protocol [ Time Frame: 8 week follow up ]Adherence is defined as completing 1 or more EMA assessments per day (total ≥56) for the duration of the 8-week EMA protocol
- Number of participants who score above threshold on Treatment Acceptability Measure [ Time Frame: 8-week posttreatment visit ]Acceptability of treatment will be measured by a questionnaire designed for use in this study.
- Number of participants who have ≥ 50% reduction in frequency of cannabis use [ Time Frame: Ad lib monitoring period (up to 2 weeks), 8-week posttreatment visit ]To evaluate if this milestone has been met, the investigators will calculate the percentage reduction in bioverified abstinent days by comparing the ad lib monitoring period to the mobile CM period.
- Average number of days since last cannabis use [ Time Frame: 8-week posttreatment visit ]Investigators will use count-adjusted (i.e., negative binomial or Poisson) MLM to model the equivalent number of joints/gram smoked on a given day as a function of days since last use.
- Number of participants who have ≥ 50% reduction in quantity of cannabis use [ Time Frame: Ad lib monitoring period (up to 2 weeks), 8-week posttreatment visit ]To evaluate if this milestone has been met, the investigators will calculate the percentage reduction in overall cannabis quantity by comparing the ad lib monitoring period to the mobile CM period.

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Ages Eligible for Study: | 18 Years to 70 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- cannabis use on ≥40 of past 90 days
- ability to speak and write fluent English
- 18-70 years of age
- willingness to attempt to temporarily reduce cannabis use
Exclusion Criteria:
- expect to have an unstable medication regimen during the study
- are currently receiving non-study CUD treatment
- meet criteria for serious mental illness (e.g., bipolar disorder, schizophrenia)
- become imprisoned
- become hospitalized for psychiatric reasons
- become pregnant
- report imminent risk for suicide or homicide
- meet criteria for a substance use disorder other than CUD or tobacco

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03681353
United States, North Carolina | |
Duke University Medical Center | |
Durham, North Carolina, United States, 27706 |
Responsible Party: | Duke University |
ClinicalTrials.gov Identifier: | NCT03681353 |
Other Study ID Numbers: |
Pro00100100 |
First Posted: | September 24, 2018 Key Record Dates |
Last Update Posted: | November 5, 2020 |
Last Verified: | September 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Plan Description: | There is no plan to share individual participant data. |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Marijuana Abuse Substance-Related Disorders Chemically-Induced Disorders Mental Disorders |