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Intervention to Reduce Injection Drug Use

Intervention to Reduce Injection Drug Use

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00786630
Enrollment
726
Registered
2008-11-06
Start date
2007-11-30
Completion date
2013-02-28
Last updated
2014-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Abuse

Keywords

Drug treatment entry and retention, Drug injection frequency, HIV risk behaviors, Hepatitis C risk behaviors

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.

Interventions

Clients will receive counseling and/or referrals for help with nine life domains (life skills, finances, leisure activities, relationships, living arrangements, occupation/education, health, mental health, recovery from substances, legal assistance) for a period of five months after baseline.

BEHAVIORALCase management plus facilitated treatment alliance

Clients will receive counseling and/or referrals for help with nine life domains (life skills, finances, leisure activities, relationships, living arrangements, occupation/education, health, mental health, recovery from substances, legal assistance) for a period of five months after baseline. They will also receive a facilitated treatment alliance, which consists of meetings with methadone counselors to aid in treatment entry.

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Exclusion criteria

* too intoxicated or impaired mentally to voluntarily consent to participate in the project and/or respond to the interview

Design outcomes

Primary

MeasureTime frame
Treatment entry and retentionBaseline, 6 months after baseline, 12 months after baseline

Secondary

MeasureTime frame
Drug injection and HIV/HCV risk behaviorsBaseline, 6 months after baseline, 12 months after baseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026