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The Rhode Island Prescription and Illicit Drug Study (RAPIDS)

Primary Purpose

Opioid Overdose, Drug Overdose

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
RAPIDS Intervention
Standard OEND
Sponsored by
Brown University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Opioid Overdose focused on measuring Drug overdose, Substance-Related Disorders, Chemically-induced disorders, Fentanyl, analgesics, Opioids, Narcotics, Naloxone, Central Nervous System Depressants, Physiological Effects of Drugs

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Brown University School of Public HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

RAPIDS intervention

Standard OEND

Arm Description

Participants randomized to receive the RAPIDS intervention will receive a fentanyl specific behavioral intervention and a brief behavioral intervention to increase willingness to use fentanyl test strips and engage in overdose risk reduction behaviors, in addition to standard OEND.

In the control arm participants will receive standard overdose education and naloxone distribution (OEND).

Outcomes

Primary Outcome Measures

Accidental non-fatal overdose in the past month
The rate of self-reported, non-fatal opioid related overdose, measured by survey questions at each follow up visit.
Accidental non-fatal overdose in the past month
The rate of self-reported, non-fatal opioid related overdose, measured by survey questions at each follow up visit.

Secondary Outcome Measures

The number of fatal overdose events
The number of fatal overdoses experienced throughout 12 month enrollment in the study, measured using Rhode Island Department of Health data

Full Information

First Posted
March 2, 2020
Last Updated
May 26, 2023
Sponsor
Brown University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT04372238
Brief Title
The Rhode Island Prescription and Illicit Drug Study
Acronym
RAPIDS
Official Title
The Rhode Island Prescription and Illicit Drug Study Responding to Fentanyl and Associated Harms
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 3, 2020 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Brown University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief 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)
Detailed Description
The investigators will assess the efficacy of the RAPIDS intervention on preventing overdose among PWUD. Participants will be randomized 1:1 to receive the RAPIDS intervention or the attention-matched control condition. Experimental arm participants will receive the RAPIDS intervention, which includes education about the dangers of illicitly manufactured fentanyl (IMF), motivational interviewing to increase willingness to use fentanyl test strips and engage in overdose risk reduction behaviors, hands-on training to use the test strips, and opportunities to plan and role- play how to implement overdose risk reduction behaviors upon receipt of a positive or negative test result. In the attention-matched control arm, participants will receive standardized overdose education and naloxone distribution (OEND) training. All participants will attend additional study visits at months 1,2,3,6, and 12. The primary endpoint will be the rate of self-reported overdose over the follow-up period. Secondary endpoints (e.g., overdose death) will be ascertained by data linkage to statewide overdose surveillance databases. The primary aims of this study are to: 1) Assess the efficacy of the RAPIDS intervention in reducing rates of overdose among people who use drugs; 2) Examine the degree to which reductions in rates of overdose are mediated by increases in information, motivation, behavioral skills, and self-efficacy regarding fentanyl, rapid fentanyl testing, and harm reduction practices; and 3) Explore whether there is heterogeneity of treatment effect related to key participant characteristics.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Overdose, Drug Overdose
Keywords
Drug overdose, Substance-Related Disorders, Chemically-induced disorders, Fentanyl, analgesics, Opioids, Narcotics, Naloxone, Central Nervous System Depressants, Physiological Effects of Drugs

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants randomized to receive the RAPIDS intervention will receive fentanyl test strips and additional fentanyl-specific education. Both arms will receive standardized overdose prevention education and naloxone.
Masking
Outcomes Assessor
Masking Description
The biostatistician will be blinded to the intervention/control group assignment throughout the course of the study and the assignments.
Allocation
Randomized
Enrollment
509 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RAPIDS intervention
Arm Type
Experimental
Arm Description
Participants randomized to receive the RAPIDS intervention will receive a fentanyl specific behavioral intervention and a brief behavioral intervention to increase willingness to use fentanyl test strips and engage in overdose risk reduction behaviors, in addition to standard OEND.
Arm Title
Standard OEND
Arm Type
Active Comparator
Arm Description
In the control arm participants will receive standard overdose education and naloxone distribution (OEND).
Intervention Type
Behavioral
Intervention Name(s)
RAPIDS Intervention
Intervention Description
RAPIDS intervention combines a behavioral intervention along with hands-on training to use fentanyl test strips.
Intervention Type
Behavioral
Intervention Name(s)
Standard OEND
Intervention Description
In the attention-matched control arm, participants will receive standardized overdose education and naloxone distribution (OEND) training, with attention-control visits at 1, 2, and 3 months. Participants will receive a naloxone kit after completion of the first session, and information regarding where to obtain additional naloxone at subsequent visits. They will have contact with study staff at month 6 and 12 follow-up visits to capture outcome and covariate data.
Primary Outcome Measure Information:
Title
Accidental non-fatal overdose in the past month
Description
The rate of self-reported, non-fatal opioid related overdose, measured by survey questions at each follow up visit.
Time Frame
6 months post-randomization
Title
Accidental non-fatal overdose in the past month
Description
The rate of self-reported, non-fatal opioid related overdose, measured by survey questions at each follow up visit.
Time Frame
12 months post-randomization
Secondary Outcome Measure Information:
Title
The number of fatal overdose events
Description
The number of fatal overdoses experienced throughout 12 month enrollment in the study, measured using Rhode Island Department of Health data
Time Frame
12 months post-randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brandon DL Marshall, PhD
Phone
401-863-6427
Email
Brandon_marshall@brown.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brandon DL Marshall, PhD
Organizational Affiliation
Brown University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brown University School of Public Health
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02912
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jacqueline E Goldman, ScM
Phone
401-863-6970
Email
jacqueline_goldman1@brown.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30344005
Citation
Krieger MS, Goedel WC, Buxton JA, Lysyshyn M, Bernstein E, Sherman SG, Rich JD, Hadland SE, Green TC, Marshall BDL. Use of rapid fentanyl test strips among young adults who use drugs. Int J Drug Policy. 2018 Nov;61:52-58. doi: 10.1016/j.drugpo.2018.09.009. Epub 2018 Oct 18.
Results Reference
background
PubMed Identifier
33243291
Citation
Jacka BP, Goldman JE, Yedinak JL, Bernstein E, Hadland SE, Buxton JA, Sherman SG, Biello KB, Marshall BDL. A randomized clinical trial of a theory-based fentanyl overdose education and fentanyl test strip distribution intervention to reduce rates of opioid overdose: study protocol for a randomized controlled trial. Trials. 2020 Nov 26;21(1):976. doi: 10.1186/s13063-020-04898-8.
Results Reference
derived

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The Rhode Island Prescription and Illicit Drug Study

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