search
Back to results

Naltrexone and Behavioral Drug and HIV Risk Reduction Counseling in Russia

Primary Purpose

Opiate Dependence

Status
Completed
Phase
Phase 3
Locations
Russian Federation
Study Type
Interventional
Intervention
Vivitrol
Naltrexone (oral)
BDRC
Medical Management
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opiate Dependence

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Detoxified volunteers seeking drug rehabilitation treatment will be eligible for the study

Exclusion Criteria:

  • Current suicide or homicide risk
  • Current psychotic disorder or major depression
  • Inability to understand the consent form or assessments
  • Pregnancy
  • Acute hepatitis, liver failure, or liver enzymes greater than 3 times the upper limit of normal.

Sites / Locations

  • Pavlov University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Vivitrol + BDRC

Vivitrol + Medical Management

Naltrexone (oral)+BDRC

Naltrexone (oral) + Medical Management

Arm Description

Outcomes

Primary Outcome Measures

reductions in sex- and drug-related HIV risk behaviors
reductions in illicit opiate use (maximum consecutive days of abstinence following detoxification and number of days of heroin or illicit opiate use in the past 30 days)
treatment retention (time to last clinical contact during outpatient treatment phase

Secondary Outcome Measures

reductions in illicit use of other drugs
improvements in vocational, family, social functioning, and quality of life indices

Full Information

First Posted
July 5, 2011
Last Updated
January 9, 2018
Sponsor
Yale University
Collaborators
St. Petersburg State Pavlov Medical University, National Institute on Drug Abuse (NIDA)
search

1. Study Identification

Unique Protocol Identification Number
NCT01389167
Brief Title
Naltrexone and Behavioral Drug and HIV Risk Reduction Counseling in Russia
Official Title
Naltrexone and Behavioral Drug and HIV Risk Reduction Counseling in Russia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
May 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Yale University
Collaborators
St. Petersburg State Pavlov Medical University, National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The long-term goals of this study are to foster development and dissemination of evidence-based behavioral and pharmacological treatments to reduce HIV transmission, injection drug use (IDU), and heroin use in Russia. This study will examine the effects of combining behavioral therapy with naltrexone pharmacotherapy for the treatment of opiate dependence and reduction of HIV risks in opiate dependent individuals. Specifically the study will determine whether extended-release injection naltrexone has greater efficacy and is more cost-effective than oral naltrexone maintenance, whether behavioral drug and HIV risk reduction counseling (BDRC) combined with brief, medical management (MM) has greater efficacy and is more cost-effective than MM only, and whether particular combinations of medication formulation and counseling (MM only or MM plus BDRC) have greater efficacy or are more cost-effective than other combinations.
Detailed Description
With an estimated 1.6-4 million opiate users (majority with injection drug use (IDU)) and more than 940,000 HIV infected individuals (80% linked to IDU), the Russian Federation is facing the prospect of an explosive HIV epidemic. Currently in Russia, inpatient detoxification followed by oral naltrexone maintenance (NMT) is the only pharmacologic treatment for opiate dependence. Evidence-based counseling to reduce HIV transmission and relapse following detoxification is not widely available or routinely provided. Several considerations, including data from our preliminary studies, suggest that the efficacy of NMT may be improved by using extended-release naltrexone (XR/NTX) instead of oral naltrexone (O/NTX) and by combining NMT with behavioral drug and HIV risk reduction counseling (BDRC). BDRC may also improve medication adherence and promote behavioral change leading to reduced relapse risk, IDU, and other drug- and sex-related HIV risk behaviors. However, the efficacy and cost-effectiveness for reducing drug- and sex-related HIV risk behaviors and increasing duration of opioid abstinence of the various combinations of naltrexone formulation (O/NTX vs. XR/NTX) and counseling (MM only or combined with BDRC) have not been systematically evaluated. Consequently, we are proposing a 2x2 factorial randomized clinical trial evaluating the efficacy and cost-effectiveness of two medication formulations (O/NTX and XR/NTX) and two manual-guided counseling conditions (MM only or MM+BDRC) and the potential interactions between medications and counseling conditions. Following detoxification, opiate dependent subjects (N=320) will be randomly assigned to 6 months of treatment in one of four treatment groups: O/NTX+MM, XR/NTX+MM, O/NTX+MM+BDRC, or XR/NTX+MM+BDRC. Primary outcome measures include reductions in sex- and drug-related HIV risk behaviors, reductions in illicit opiate use, and treatment retention. Other outcome measures include reductions in frequency of opiate or other drug use, health status and healthcare utilization, criminal behavior and arrests, and improvements in vocational and family functioning and quality of life. All study participants will be assessed at baseline and monthly during the 6 month treatment phase and for 6 months following the active treatment phase. Data analyses will focus on the intention-to treat sample. The study results will allow evaluation of whether XR/NTX has superior efficacy or is more cost-effective than O/NTX, whether BDRC plus MM has superior efficacy or is more cost-effective than MM only, and whether particular combinations of medications and counseling have superior efficacy or are more cost-effective than other combinations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opiate Dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
320 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vivitrol + BDRC
Arm Type
Experimental
Arm Title
Vivitrol + Medical Management
Arm Type
Experimental
Arm Title
Naltrexone (oral)+BDRC
Arm Type
Experimental
Arm Title
Naltrexone (oral) + Medical Management
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Vivitrol
Intervention Description
An extended release naltrexone formulation for intramuscular injection
Intervention Type
Drug
Intervention Name(s)
Naltrexone (oral)
Intervention Description
Naltrexone 50 mg pills, daily
Intervention Type
Behavioral
Intervention Name(s)
BDRC
Intervention Description
Manual-guided BDRC is a highly structured, educational, prescriptive, and individualized treatment that focuses on the patient's current problem areas that are immediately related to marinating abstinence in order to achieve sustained recovery from drugs. The primary goals of BDRC include education about the disease of opiate dependence and effective treatment approaches, skills and strategies to maintain drug abstinence following detoxification, reduction/cessation of drug and sexual behaviors associated with HIV transmission, and increased engagement in non-drug-related social interactions and pleasurable activities.
Intervention Type
Behavioral
Intervention Name(s)
Medical Management
Intervention Description
Patient assigned to MM will receive manual-guided medically oriented counseling approximating the current standard of care provided in with NTM the Russian Federation, consisting of an initial introductory session (introduction to NMT and basic education about HIV risks) and subsequent, brief (up to 20 minutes) support and advice sessions once per month.
Primary Outcome Measure Information:
Title
reductions in sex- and drug-related HIV risk behaviors
Time Frame
every month during 6 months of active study phase and during the 6 month follow-up
Title
reductions in illicit opiate use (maximum consecutive days of abstinence following detoxification and number of days of heroin or illicit opiate use in the past 30 days)
Time Frame
every month during 6 months of active study phase and during the 6 month follow-up
Title
treatment retention (time to last clinical contact during outpatient treatment phase
Time Frame
6 months
Secondary Outcome Measure Information:
Title
reductions in illicit use of other drugs
Time Frame
every month during 6 months of active study phase and during the 6 month follow-up
Title
improvements in vocational, family, social functioning, and quality of life indices
Time Frame
every month during 6 months of active study phase and during the 6 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Detoxified volunteers seeking drug rehabilitation treatment will be eligible for the study Exclusion Criteria: Current suicide or homicide risk Current psychotic disorder or major depression Inability to understand the consent form or assessments Pregnancy Acute hepatitis, liver failure, or liver enzymes greater than 3 times the upper limit of normal.
Facility Information:
Facility Name
Pavlov University
City
St. Petersburg
Country
Russian Federation

12. IPD Sharing Statement

Learn more about this trial

Naltrexone and Behavioral Drug and HIV Risk Reduction Counseling in Russia

We'll reach out to this number within 24 hrs