Contingency Management for Cannabis Use for Persons With HIV
NCT ID: NCT04866004
Last Updated: 2025-09-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
25 participants
INTERVENTIONAL
2021-08-01
2025-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Contingency Management - Cannabis
Participants will be incentivized following biochemical verification (from urine samples) of cannabis abstinence.
Contingency Management - Cannabis
Participants in the contingency management program will be provided financial incentives for 28-days of cannabis abstinence. At every visit, participants will provide urine samples for the biochemical verification of cannabis abstinence). Participants with evidence of cannabis abstinence will be provided a financial incentive that increases across subsequent study visits.
Interventions
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Contingency Management - Cannabis
Participants in the contingency management program will be provided financial incentives for 28-days of cannabis abstinence. At every visit, participants will provide urine samples for the biochemical verification of cannabis abstinence). Participants with evidence of cannabis abstinence will be provided a financial incentive that increases across subsequent study visits.
Eligibility Criteria
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Inclusion Criteria
* Self-report of cannabis use at least once per week in the 6-month period prior to consent
* Provide a positive urine toxicology (UTOX) screen for cannabis
* Not seeking treatment for cannabis use
* Willing to stop using cannabis for 28 days and attend eight study visits over six weeks.
* Ability and willingness to provide inform consent
* English fluency
Exclusion Criteria
* Diagnosed or receiving treatment for a current major depressive or anxiety disorder
* Diagnosed with any current alcohol or substance use disorder (excluding nicotine) using the Structured Clinical Interview for Clinical Disorders (SCID) Interview (22)
* Positive UTOX screen for opioids
* Having a medical, psychiatric, occupational, or other condition that, in the judgment of the study physician, would make participation difficult or unsafe.
18 Years
ALL
No
Sponsors
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The University of Texas Health Sciences Center, Houston
UNKNOWN
National Institute on Drug Abuse (NIDA)
NIH
The University of Texas Health Science Center at San Antonio
OTHER
Responsible Party
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Chukwuemeka Okafor
Assistant Professor
Principal Investigators
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Chukwuemeka N Okafor, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center at San Antonio
Locations
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Center for Neurobehavioral Research on Addiction
Houston, Texas, United States
University of Texas Health Science Center at San Antonio
San Antonio, Texas, United States
Countries
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Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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HSC20220688H
Identifier Type: OTHER
Identifier Source: secondary_id
HSC-MS-20-0886
Identifier Type: -
Identifier Source: org_study_id
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