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Clinical Trials/NCT00596843
NCT00596843CompletedPhase 3

Chronic Hepatitis Intervention Project for Drug Users

National Institute on Drug Abuse (NIDA)1 site in 1 country851 target enrollmentStarted: September 1, 2003Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
851
Locations
1
Primary Endpoint
Reduction/cessation of alcohol use

Study Overview

Brief Summary

The purpose of this study is to determine if a 6-session motivational interviewing intervention is more effective than a 6-session educational intervention at reducing behaviors that may lead to infection, transmission, and progression of HIV and hepatitis C among out of treatment injecting drug users.

Detailed Description

This 4.5-year community-based study is a randomized field experiment that uses a two-group design. Participants are randomized into either an Educational intervention group or a Motivational intervention group. We are comparing the effectiveness of the Motivational intervention with the Educational intervention. We are also estimating the costs and evaluating the cost-effectiveness of the Motivational intervention relative to the Educational intervention.

We have the following aims and related hypotheses:

Aim 1: To compare the effectiveness of a 6-session personalized motivational intervention to a 6-session educational intervention in terms of injection risk, sexual behavior, alcohol use, and knowledge and perception related to HBV and HCV; H1. Relative to the Educational intervention group, a greater proportion of the Motivational intervention group will report no injection risk at 6- and 12-month follow-up interviews. No injection risk is operationally defined as either no injections in the past 30 days, or no direct or indirect sharing of syringes and other injection equipment in the past 30 days.

H2. Relative to the Educational intervention group, a greater proportion of the Motivational intervention group will report no sexual risk at 6- and 12-month follow-up interviews. No sexual risk is operationally defined as either no sex (oral, vaginal, or anal) in the past 30 days, or no unprotected oral, vaginal, or anal sex in the past 30 days.

H3. Relative to the Educational intervention group, the Motivational intervention group will report greater decreases in frequency of alcohol consumption and quantity of alcohol consumed. Frequency of alcohol consumption is defined as "number of days drank alcohol in the past 30 days," and quantity of alcohol consumed is defined as "the average number of drinks per drinking day during the past 30 days." H4. Relative to the Educational intervention group, participants in the Motivational intervention group will report greater increases in knowledge and more accurate perceptions of severity of disease and efficacy of protective actions regarding hepatitis B and C at Session 3.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •minimum age of 18 years injected illicit drugs within last 30 days

Exclusion Criteria

  • •participated in formal substance treatment in last 30 days

Arms & Interventions

1

Experimental

Motivational intervention

Intervention: Motivational interviewing (Behavioral)

2

Active Comparator

Educational intervention

Intervention: Educational intervention (Behavioral)

Outcomes

Primary Outcomes

Reduction/cessation of alcohol use

Time Frame: 6-months and 12-months

Secondary Outcomes

  • Reductions in unprotected sexual behavior(6-months and 12-months)
  • Reductions in direct and indirect needle and syringe sharing(6-months and 12-months)

Investigators

Sponsor Class
Nih
Responsible Party
Sponsor

Study Sites (1)

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