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The Staying Safe Intervention (Ssafe)

Primary Purpose

Hepatitis C, Opioid Use

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Staying Safe (Ssafe)
Healthy Living
Sponsored by
National Development and Research Institutes, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis C focused on measuring People who inject drugs, Hepatitis C prevention, Young adults, Behavioral interventions

Eligibility Criteria

18 Years - 29 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Staying Safe Study 235 Eldridge StreetRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Staying Safe (Ssafe)

Healthy Living

Arm Description

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.

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.

Outcomes

Primary Outcome Measures

Injection risk behavior: Syringe-sharing
number of times receptively shared syringes
Injection risk behavior: Syringe-sharing partners
number of people receptively shared syringes with
Injection risk behavior: Secondary injection equipment-sharing
number of times receptively shared secondary injection equipment (including cookers, cottons, water and water containers combined)
Injection risk behavior: Secondary injection equipment-sharing partners
number of people receptively shared secondary injection equipment with (including cookers, cottons, water and water containers combined)
Injection risk behavior: Backloading
number of times backloaded
Injection risk behavior: Backloading partners
number of people backloaded with

Secondary Outcome Measures

Hepatitis C incidence
hepatitis C antibody-positive rapid test result (OraQuick)
Overdose events
opioid-related episodes involving loss of consciousness, non-responsiveness and/or administration of naloxone
Injection frequency
average number of daily and monthly injections
Injection-related complications
number and type of physical complications from injection drug use

Full Information

First Posted
January 12, 2018
Last Updated
May 9, 2018
Sponsor
National Development and Research Institutes, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT03418636
Brief Title
The Staying Safe Intervention
Acronym
Ssafe
Official Title
The Staying Safe Intervention: Preventing HCV Among Young Opioid Injectors
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 31, 2018 (Actual)
Primary Completion Date
May 31, 2021 (Anticipated)
Study Completion Date
May 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Development and Research Institutes, Inc.

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
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis C, Opioid Use
Keywords
People who inject drugs, Hepatitis C prevention, Young adults, Behavioral interventions

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
456 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Staying Safe (Ssafe)
Arm Type
Experimental
Arm Description
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.
Arm Title
Healthy Living
Arm Type
Active Comparator
Arm Description
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 Type
Behavioral
Intervention Name(s)
Staying Safe (Ssafe)
Intervention Description
Staying Safe motivates and teaches young people who inject drugs (PWID) planning skills and drug use management strategies to enable long-term risk avoidance and the implementation of healthy protective behaviors. Content is presented through guided discussions and role playing exercises, and relies heavily on interactive participation by group members to foster peer-based learning and social reinforcement processes.
Intervention Type
Behavioral
Intervention Name(s)
Healthy Living
Intervention Description
The content of the Healthy Living intervention is based on the DHHS' Eat Healthy, Be Active Community Workshop curriculum, supplemented with basic sleep hygiene education. Science-based dietary and light physical activity guidelines are demonstrated and promoted to help participants develop and maintain a healthy lifestyle.
Primary Outcome Measure Information:
Title
Injection risk behavior: Syringe-sharing
Description
number of times receptively shared syringes
Time Frame
3 months
Title
Injection risk behavior: Syringe-sharing partners
Description
number of people receptively shared syringes with
Time Frame
3 months
Title
Injection risk behavior: Secondary injection equipment-sharing
Description
number of times receptively shared secondary injection equipment (including cookers, cottons, water and water containers combined)
Time Frame
3 months
Title
Injection risk behavior: Secondary injection equipment-sharing partners
Description
number of people receptively shared secondary injection equipment with (including cookers, cottons, water and water containers combined)
Time Frame
3 months
Title
Injection risk behavior: Backloading
Description
number of times backloaded
Time Frame
3 months
Title
Injection risk behavior: Backloading partners
Description
number of people backloaded with
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Hepatitis C incidence
Description
hepatitis C antibody-positive rapid test result (OraQuick)
Time Frame
12 months
Title
Overdose events
Description
opioid-related episodes involving loss of consciousness, non-responsiveness and/or administration of naloxone
Time Frame
3 months
Title
Injection frequency
Description
average number of daily and monthly injections
Time Frame
30 days
Title
Injection-related complications
Description
number and type of physical complications from injection drug use
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Injection network size
Description
number of people injected with (i.e., in the presence of these people)
Time Frame
3 months
Title
Motivation/Self-efficacy to inject safely and manage opioid intake
Description
Total score on the Staying Safe Self-Efficacy Scale (8 items; possible score range = 0-32), an investigator-developed and validated instrument (Mateu-Gelabert et al., 2014).
Time Frame
3 months
Title
OUD treatment participation
Description
participation in Medication-Assisted Treatment (MAT) for Opioid Use Disorder (OUD)
Time Frame
3 months
Title
Opioid withdrawal
Description
frequency of opioid withdrawal episodes
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
29 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Honoria Guarino, PhD
Phone
212-845-4540
Email
guarino@ndri.org
First Name & Middle Initial & Last Name or Official Title & Degree
Ramona Almenana, MPA
Email
almenana@ndri.org
Facility Information:
Facility Name
Staying Safe Study 235 Eldridge Street
City
New York
State/Province
New York
ZIP/Postal Code
10002
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ramona Almenana, MPA
Phone
917-261-6456
Email
almenana@ndri.org
First Name & Middle Initial & Last Name & Degree
Elizabeth Goodbody, BA
Phone
917-261-6456
Email
goodbody@ndri.org

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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