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N/A N=509 Randomized Single-blind Prevention

The Rhode Island Prescription and Illicit Drug Study

Opioid Overdose · Drug Overdose

Enrolled (actual)
509
Serious AEs
5.5%
Results posted
Aug 2025
Primary outcome: Primary: Number of People Identified Has Having One or More Overdose Among RAPIDS Trial Participants — 48; 36 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
RAPIDS Intervention (Behavioral); Standard OEND (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Brown University
Primary completion
Feb 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of People Identified Has Having One or More Overdose Among RAPIDS Trial Participants
48; 36
PRIMARY
Accidental Non-fatal Overdose in the Past Month
5.4; 2.7; 5.6; 4.6; 3.4; 4.0
SECONDARY
The Number of Fatal Overdose Events
9; 7
SECONDARY
Number of Participants With Positive Dry Blood Spot Samples
34; 35; 86; 79; 125; 128

Summary

This study will test the efficacy of a novel drug-checking intervention to prevent fatal and non-fatal overdose among people who use drugs (PWUD), who are 18-65 years old at the time of enrollment. The investigators will evaluate whether the incorporation of rapid fentanyl testing into a theory-driven overdose education and prevention intervention reduces rates of overdose compared to standard overdose education and naloxone distribution. Results from this study will significantly improve public health efforts to address the fentanyl overdose epidemic and reduce harms associated with exposure to drugs contaminated with fentanyl. This is a full clinical trial, building on the previously approved fentanyl-test-strip pilot study (2016-2017), the results of which have recently been published.(Krieger et al., 2018)

Eligibility Criteria

Inclusion Criteria

  • Reside in Rhode Island
  • Are able to complete interviews in English
  • Are able to provide informed consent
  • Self-report past 30 day heroin, illicit stimulants, counterfeit prescription pills, or injection drugs

Exclusion Criteria

  • Participants who exclusively misuse medications obtained from a physician or diversion from someone else's prescription
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04372238). 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.

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