Mode
Text Size
Log in / Sign up
N/A Completed N=720 Randomized Health Services Research

Building on Needle Exchange to Optimize Prevention & Treatment

Intravenous Drug Usage · HIV
Source: ClinicalTrials.gov NCT03567174 ↗
Enrolled (actual)
720
Serious AEs
7.6%
Results posted
Dec 2022
Primary outcomePrimary: Composite PWID Score (Service Access, Risk Behaviors, Adverse Outcomes) — 5.34; 5.64 units on a scale — p=0.125

Summary

There are several biomedical interventions that can help people who inject drugs (particularly those with or at risk for HIV), but these services often do not get to the people most in need. In this project investigators propose to determine if delivery of these services to PWID by an integrated care van that is linked to a mobile syringe service program improves clinical outcomes, is feasible and sustainable, and is cost-effective.

Outcome Measures

OutcomeResultp-value
PRIMARY
Composite PWID Score (Service Access, Risk Behaviors, Adverse Outcomes)
5.34; 5.64 0.125
SECONDARY
HIV Care Continuum
13; 19; 18; 10; 1; 4
SECONDARY
HIV Testing
234; 202; 2; 8
SECONDARY
Pre-exposure Prophylaxis (PrEP) Continuum
0; 4; 236; 206
SECONDARY
HCV Care Continuum
34; 20; 36; 25; 75; 58
SECONDARY
HCV Testing
65; 66; 57; 73
SECONDARY
Medication for Opioid Use Disorder (MOUD) Use
165; 134; 103; 109
SECONDARY
Syringe Service Program (SSP) Use
223; 208; 45; 35
SECONDARY
Naloxone Overdose Kit
164; 157; 104; 86
SECONDARY
Injection Drug Use
108; 85; 160; 158
SECONDARY
Recent Drug Use
42; 25; 225; 217
SECONDARY
Sharing Injection Equipment
202; 175; 21; 23; 45; 45
SECONDARY
Non-fatal Overdose
230; 210; 38; 33
SECONDARY
Emergency Department (ED) Use
166; 144; 102; 99
SECONDARY
HIV Seroconversion
236; 210; 1; 1
SECONDARY
HCV Seroconversion
87; 105; 1; 6
SECONDARY
Mortality Rate
268; 243; 4; 7

Eligibility Criteria

Inclusion Criteria

  • If HIV-positive: report history of injection drug use
  • If HIV-negative: injected drugs ≥ 4 days in the last 30 days or shared a needle or syringe in the last 6 months

Exclusion Criteria

  • Not competent to provide written informed consent
  • Not willing or able to provide a blood specimen
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03567174). 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. Informational only — not medical advice.

Back to search