Evidence map›Paper›PMID 42624166›Full record

ArticlePreventive medicine2026

A pilot trial of contingency management for stimulant use in a low-barrier syringe service program.

Tyler G Erath, Katya Marsh, Erin O'Keefe, Michael Desarno, Stephen T Higgins, Richard A Rawson

Abstract read
In one paragraph

Article in Preventive medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tyler G ErathVermont Center on Behavior and Health, Burlington, VT, USA; Department of Psychiatry, University of Vermont, Burlington, VT, USA. Electronic address: tyler.erath@uvm.edu.
Katya MarshVermont Center on Behavior and Health, Burlington, VT, USA; Howard Center Safe Recovery, Burlington, VT, USA.
Erin O'KeefeHoward Center Safe Recovery, Burlington, VT, USA.
Michael DesarnoMedical Biostatistics, University of Vermont, Burlington, VT, USA.
Stephen T HigginsVermont Center on Behavior and Health, Burlington, VT, USA; Department of Psychiatry, University of Vermont, Burlington, VT, USA; Center on Rural Addictions, University of Vermont, Burlington, VT, USA.
Richard A RawsonVermont Center on Behavior and Health, Burlington, VT, USA; Department of Psychiatry, University of Vermont, Burlington, VT, USA; Center on Rural Addictions, University of Vermont, Burlington, VT, USA.

Funding

Vermont Center on Behavior and HealthP20GM103644 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI HIGGINS, STEPHEN T · 2013 to 2022
$21.3M
TRAINING IN BEHAV. PHARMACOLOGY OF HUMAN DRUG DEPENDENCET32DA007242 · NIDA · UNIVERSITY OF VERMONT &ST AGRIC COLLEGE · PI HEIL, SARAH H, HIGGINS, STEPHEN T · 1990 to 2025
$8.2M
Vermont Center on Behavior and HealthP30GM149331 · NIGMS · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Stephen T Higgins · 2023 to 2026
$5.6M
Using Implementation Science to Advance Evidence-Based Treatment for Stimulant Use K01DA060309 · NIDA · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Tyler George Erath · 2025 to 2026
$405k
NIDA NIH HHS K01 DA060309NIDA NIH HHS T32 DA007242NIGMS NIH HHS P20 GM103644NIGMS NIH HHS P30 GM149331
6 · The paper itself

Abstract

objectiveTo pilot test the efficacy of contingency management (CM) for stimulant use disorder (StimUD) among syringe service program (SSP) recipients.

methodsThis randomized, parallel-groups, 12-week pilot trial was conducted in Burlington, Vermont from 02/24-07/24. Twenty-seven individuals with StimUD participating in SSP services were randomized to health education (HE) plus CM for session attendance (HE+Att-CM) (n = 13) or HE plus CM for stimulant abstinence (HE+Abs-CM) (n = 14). Stimulant use monitoring was examined twice-weekly using point-of-care urine drug tests (UDTs). HE+Att-CM participants earned incentives for UDT samples independent of results. HE+Abs-CM participants earned incentives for stimulant-negative UDT samples. The primary outcome was the percentage of participants stimulant-negative by week. Missing UDTs were treated as stimulant positive. Outcomes were compared between conditions using repeated measures mixed models for categorical data based on generalized estimating equations using a logistic link function.

resultsThe percentage of participants stimulant-negative was greater in the HE+Abs-CM condition averaging 22.6% (weekly range, 7.1%-28.6%) compared to 3.2% (weekly range, 0%-7.7%) in the HE+Att-CM condition (p = .014).

conclusionsFindings provide preliminary experimental evidence that CM reduces stimulant use among individuals participating in low-barrier services at a community-based SSP.

Indexed as

Contingency managementLow barrierPolysubstance useStimulant use disorderStimulant use treatmentSyringe service program

Identifiers

PMID42624166
PMCPMC13537421

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.