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Clinical Trials/NCT05787847
NCT05787847
Completed
N/A

Financial Incentives to Promote Stimulant Abstinence in a Community-Based Syringe Exchange Program

University of Vermont1 site in 1 country27 target enrollmentFebruary 14, 2024
ConditionsStimulant Use

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stimulant Use
Sponsor
University of Vermont
Enrollment
27
Locations
1
Primary Endpoint
Stimulant Free Urine Sample
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

The goal of this randomized control pilot study is to learn about a financial incentives intervention among individuals who use stimulants and take part in a community-based syringe exchange program. The main question it aims to answer is how financial incentives for not using stimulants will impact stimulant use. Participants in the experimental group will have the opportunity to earn financial incentives for providing a negative urine sample for stimulants using a point-of-care test, which indicates abstinence from stimulant use, along with health education on the health risks of stimulant use and substance injection. Researchers will compare the experimental group to the control group who will receive health education on the health risks of stimulants use and injection.

Detailed Description

The investigators are proposing a two condition, parallel groups, randomized control pilot study to evaluate the efficacy of a financial incentives intervention among individuals who use stimulants and take part in a community-based syringe exchange program. The study design will include recruiting service recipients who already participate in programs offered by a syringe exchange program.The experimental group will have the opportunity to earn financial incentives contingent on providing a negative urine sample for stimulants using a point-of-care test, which indicates abstinence from stimulant use, in addition to health education on the health risks of stimulant use and substance injection. The control group will receive health education on the health risks of stimulants use and injection. All participants will participate in their syringe exchange services as usual. The investigators chose the health education as the control because participants across both conditions already receive the services provided by the syringe exchange program. Moreover, this control condition will help control for a potential type of between-groups variability.

Registry
clinicaltrials.gov
Start Date
February 14, 2024
End Date
July 30, 2024
Last Updated
7 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

richard rawson

Research Professor

University of Vermont

Eligibility Criteria

Inclusion Criteria

  • be 18 years or older
  • report using stimulants in the past 30 days
  • meet the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) diagnosis for stimulant use disorder at a moderate or severe level (i.e., 6 or more of the 11 criteria)
  • participation in services at syringe exchange program

Exclusion Criteria

  • failure to meet one or more inclusionary criteria
  • individuals who are cognitively impaired by their drug use or psychiatric conditions that could preclude informed consent

Outcomes

Primary Outcomes

Stimulant Free Urine Sample

Time Frame: 12 weeks

all samples will be assessed using point-of-care test urine drug test conducted at the center

Study Sites (1)

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