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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05787847
Enrollment
27
Registered
2023-03-28
Start date
2024-02-14
Completion date
2024-07-30
Last updated
2025-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stimulant Use

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.

Interventions

BEHAVIORALIncentives for Abstinence

Participants in the incentives for abstinence condition will have the opportunity to earn financial incentives for abstaining from stimulant use.

BEHAVIORALHealth Education

The Health Education condition is based on a previous intervention used as a control in a number of other studies. Sessions consist of an educational program addressing a variety of health, wellness, and lifestyle topics adapted from a previously implemented wellness manual.

Sponsors

University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Stimulant Free Urine Sample12 weeksall samples will be assessed using point-of-care test urine drug test conducted at the center

Countries

United States

Participant flow

Pre-assignment details

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 * participation in services at syringe exchange program

Participants by arm

ArmCount
Health Education
The Health Education condition is based on a previous intervention used as a control in a number of other studies. Sessions consist of an educational program addressing a variety of health, wellness, and lifestyle topics adapted from a previously implemented wellness manual.
13
Health Education Plus Incentives for Abstinence
Participants in the health education plus incentives for abstinence condition will have the opportunity to earn financial incentives for abstaining from stimulant use. Additionally, they also receive the health education provided in the Health Education condition, with sessions consisting of an educational program addressing a variety of health, wellness, and lifestyle topics adapted from a previously implemented wellness manual.
14
Total27

Baseline characteristics

CharacteristicHealth EducationHealth Education Plus Incentives for AbstinenceTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
13 Participants14 Participants27 Participants
Race/Ethnicity, Customized
Race/Ethnicity
Latinx/Hispanic & Black & American Indian/Alaska Native
0 Participants1 Participants1 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White
11 Participants12 Participants23 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White & American Indian/Alaska Native
1 Participants1 Participants2 Participants
Race/Ethnicity, Customized
Race/Ethnicity
White & Black/African American
1 Participants0 Participants1 Participants
Sex/Gender, Customized
Sex/Gender
Female
6 Participants10 Participants16 Participants
Sex/Gender, Customized
Sex/Gender
Male
7 Participants4 Participants11 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 130 / 14
other
Total, other adverse events
0 / 130 / 14
serious
Total, serious adverse events
0 / 130 / 14

Outcome results

Primary

Stimulant Free Urine Sample

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

Time frame: 12 weeks

ArmMeasureValue (MEAN)Dispersion
Health EducationStimulant Free Urine Sample6.1 % stimulant-negative urine drug testStandard Error 2.7
Health Education Plus Incentives for AbstinenceStimulant Free Urine Sample23.6 % stimulant-negative urine drug testStandard Error 10.3

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026