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Clinical Trials/NCT03418636
NCT03418636UnknownNot Applicable

The Staying Safe Intervention: Preventing HCV Among Young Opioid Injectors

National Development and Research Institutes, Inc.1 site in 1 country456 target enrollmentStarted: January 31, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
456
Locations
1
Primary Endpoint
Injection risk behavior: Syringe-sharing

Study Overview

Brief Summary

The growing population of young people who inject drugs (PWID) is at extremely high risk for HCV infection through the use of contaminated injection equipment, yet, to date, no behavioral intervention has been sufficiently potent to produce significant reductions in HCV incidence among PWID. To address this critical public health need, our team developed Staying Safe (Ssafe), an innovative, strengths-based, socio-behavioral HCV prevention intervention found in preliminary research to be highly acceptable and feasible, with strong indications of efficacy. The proposed randomized, controlled trial will assess the effectiveness of the Ssafe intervention in reducing both injection-related HCV/HIV risk behavior and HCV incidence among young adults (ages 18-29) who inject opioids (heroin and/or prescription opioids).

Detailed Description

HCV infection is the most common chronic blood-borne infection in the U.S., with the overwhelming majority of new HCV infections occurring among people who inject drugs (PWID). Sharing syringes and other injection equipment is the primary risk factor for HCV transmission. HCV prevalence is extremely high in most U.S. PWID populations (typically ranging from ~40-70%). Research shows that young PWID (under age 30) engage in particularly high rates of risky injection, and that HCV incidence is highest in the first 3-5 years of an individual's injection career. The national significance of this public health problem is heightened by the recent epidemic of prescription opioid (PO) misuse in youth which has evolved into widespread heroin use and injection drug use, creating a new generation of young injectors at risk for HCV (and HIV). These trends demonstrate the urgent need for innovative new approaches to HCV prevention tailored to the growing population of young PWID.

To date, no behavioral intervention has been sufficiently potent to produce significant reductions in HCV incidence in at-risk groups of PWID. To address this critical gap, our team developed Staying Safe (Ssafe), an innovative, strengths-based, socio-behavioral HCV prevention intervention for young PWID. Ssafe addresses multi-level "upstream" determinants of risk that occur relatively early in the causal chain of risk, including eco-social conditions, social relations and risk situations, in addition to directly targeting risky injection practices. Ssafe trains and motivates PWID to better manage drug use in order to avoid situations and practices that promote risky injection (e.g., "binging" on drugs), and to implement health-protective behaviors (e.g., promoting risk-reduction norms in injection networks). In preliminary research we found Ssafe to be highly acceptable and feasible, with strong indications of efficacy.

In this study we propose to conduct a randomized controlled trial to assess the effectiveness of the Ssafe intervention (with a mobile phone-delivered booster application) in reducing injection-related risk behavior and HCV incidence among 18-29 year-olds (n=456) who inject opioids (heroin and/or POs) and test HCV and HIV antibody-negative at baseline. We hypothesize that Ssafe will significantly reduce injection risk behaviors and HCV infections relative to a time- and attention-matched control intervention. We will also examine whether Ssafe's effects are mediated by (a) drug use management practices (injection frequency, overdose, opioid intake, withdrawal episodes); (b) individual-level mechanisms of behavior change (motivation/self-efficacy, planning skills); and (c) key upstream socio-structural and network-level determinants of risk (social support, skills to avoid PWID-associated stigma, drug treatment and SEP utilization, injection network size and risk norms). The proposed trial promises to significantly advance our ability to prevent HCV infection in the growing population of young, PO-initiated injectors.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 29 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Hepatitis C antibody-negative
  • •HIV antibody-negative
  • •Have injected drugs 4 or more times in the past 30 days
  • •Current opioid use (verified by rapid urine screen)
  • •Speak English
  • •Willing to participate in assigned intervention

Exclusion Criteria

  • Not provided

Arms & Interventions

Staying Safe (Ssafe)

Experimental

Ssafe is delivered in a small group format (consisting of approximately 10-12 participants) by a trained facilitator over 4 2.5-hour sessions (10 hours total). To help promote the maintenance of risk reduction over the trial's 12-month follow-up period, Ssafe participants will be provided with a novel interactive, smartphone-delivered "booster" application based on core Ssafe principles and risk reduction strategies.

Intervention: Staying Safe (Ssafe) (Behavioral)

Healthy Living

Active Comparator

Healthy Living is a time- and attention-matched control intervention of equivalent session structure and duration as Ssafe (4 2.5-hour sessions; 10 hours total), also delivered in a small group format (10-12 participants). Healthy Living participants will be provided with a publicly available, sleep hygiene-focused smartphone app to promote healthy sleep habits over the trial's follow-up period.

Intervention: Healthy Living (Behavioral)

Outcomes

Primary Outcomes

Injection risk behavior: Syringe-sharing

Time Frame: 3 months

number of times receptively shared syringes

Injection risk behavior: Syringe-sharing partners

Time Frame: 3 months

number of people receptively shared syringes with

Injection risk behavior: Secondary injection equipment-sharing partners

Time Frame: 3 months

number of people receptively shared secondary injection equipment with (including cookers, cottons, water and water containers combined)

Injection risk behavior: Backloading

Time Frame: 3 months

number of times backloaded

Injection risk behavior: Backloading partners

Time Frame: 3 months

number of people backloaded with

Injection risk behavior: Secondary injection equipment-sharing

Time Frame: 3 months

number of times receptively shared secondary injection equipment (including cookers, cottons, water and water containers combined)

Secondary Outcomes

  • Injection frequency(30 days)
  • Hepatitis C incidence(12 months)
  • Injection-related complications(3 months)
  • Overdose events(3 months)

Investigators

Sponsor
National Development and Research Institutes, Inc.
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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