MedPath

Intervention to Reduce Injection Drug Use

Not Applicable
Completed
Conditions
Substance Abuse
Interventions
Behavioral: Strengths-based case management
Behavioral: Case management plus facilitated treatment alliance
Registration Number
NCT00786630
Lead Sponsor
University of Colorado, Denver
Brief Summary

This is a five-year prospective randomized trial comparing two intervention conditions designed to facilitate substance abuse treatment entry and enhance retention in order to reduce the behaviors associated with HIV and HCV risk among injection drug users (IDUs) and to improve client overall functioning. The overall goal of this project is to compare strengths-based case-management (CM) to an enhanced version of CM that uses case managers to facilitate a therapeutic alliance (CM/FTA) among out-of-treatment IDUs in Denver.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
726
Inclusion Criteria
  • opiate injection at least 3 times a week during the last 6-months
  • 18 years of age or older
  • no drug abuse treatment in the 30-days prior to the interview
  • not transient
  • no known reason (e.g. pending jail time) why they will not be available for follow-up interviews
  • not involved in Project Safe research activities in the previous 12 months
  • willing to meet with an Addiction Research and Treatment Services (methadone clinic) counselor
  • eligible to be treated at ARTS
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Exclusion Criteria
  • too intoxicated or impaired mentally to voluntarily consent to participate in the project and/or respond to the interview
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Case ManagementStrengths-based case management-
Facilitated Treatment AllianceCase management plus facilitated treatment alliance-
Primary Outcome Measures
NameTimeMethod
Treatment entry and retentionBaseline, 6 months after baseline, 12 months after baseline
Secondary Outcome Measures
NameTimeMethod
Drug injection and HIV/HCV risk behaviorsBaseline, 6 months after baseline, 12 months after baseline

Trial Locations

Locations (1)

Project Safe

🇺🇸

Denver, Colorado, United States

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