N/A
N=27
Financial Incentives to Promote Stimulant Abstinence in a Community-Based Syringe Exchange Program
Stimulant Use
Bottom Line
View on ClinicalTrials.gov: NCT05787847 ↗Enrolled (actual)
27
Serious AEs
0.0%
Results posted
Sep 2025
Primary outcome: Primary: Stimulant Free Urine Sample — 6.1; 23.6 % stimulant-negative urine drug test
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Incentives for Abstinence (Behavioral); Health Education (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Vermont
- Primary completion
- Jul 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Stimulant Free Urine Sample |
6.1; 23.6 | — |
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.
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
Data sourced from ClinicalTrials.gov (NCT05787847). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.