Contingency Management for Cannabis Use for Persons With HIV

  • STATUS
    Recruiting
  • End date
    Jul 1, 2023
  • participants needed
    45
  • sponsor
    Baylor University
Updated on 15 March 2022
hiv viral load
HIV Vaccine

Summary

The purpose of this study is to determine the feasibility and impact of 28-days of monitored abstinence from cannabis use on symptoms of depression and anxiety, pain, sleep, cannabis use withdrawal, HIV viral load and biomarkers of systemic inflammation among PLWH and who use cannabis regularly (weekly or more often). This will be a single arm pilot feasibility trial involving a contingency management program to induce cannabis abstinence. Specifically, the contingency management program will provide motivational (monetary) incentives to participants who achieve biochemically verified cannabis abstinence. Over the 28-days of this pilot feasibility trial, participants will attend seven study visits. During these visits, participants will complete survey questionnaires to assess sociodemographic, psychosocial, and behavioral factors. In addition, participants will provide blood and urine specimens for testing and quantitation of HIV viral load, biomarkers of systemic inflammation and for the detection of cannabis and other drugs of abuse.

Details
Condition Marijuana, HIV Infections
Treatment Contingency Management - Cannabis
Clinical Study IdentifierNCT04866004
SponsorBaylor University
Last Modified on15 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

HIV-positive (confirmed via HIV medication or relevant HIV labs in subject's name)
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

Currently receiving treatment for cannabis or other drug use disorder
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
Clear my responses

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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