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HIV and HCV Intervention In Drug Treatment Settings - 1 - Article


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Youth Risk Behavior Surveillance System

YRBSS

Clinical Trial: HIV and HCV Intervention In Drug Treatment Settings - 1

This study is currently recruiting patients.

Sponsors and Collaborators: National Institute on Drug Abuse (NIDA)
University of Colorado
Information provided by: National Institute on Drug Abuse (NIDA)

Purpose

The purpose of this study is to test two strategies to reduce the risk of contracting Human Immunodeficiency Virus (HIV) or Hepatitis C Virus (HCV) by reducing risk behaviors in patients undergoing drug detoxification.

Condition Treatment or Intervention Phase
Behavior Therapy
  Behavior: Behavior Therapy
 Phase III

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Prevention, Uncontrolled

Official Title: HIV and HCV Intervention in Drug Treatment Settings

Further Study Details: 

Expected Total Enrollment:  706

Study start: December 2003

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

Volunteers will be IV drug users already enrolled in drug detoxification treatment.

Location and Contact Information

Laetitia Thompson, Ph.D.      (303)315-2511    laetitia.thompson@uchsc.edu

Colorado
      Denver Health & Hosp Authority, Denver,  Colorado,  80204 4507,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

      Island Grove RTC, Greeley,  Colorado,  80631,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Massachusetts
      SSTAR (Stanley St. Treatment & Resources, Inc), Fall River,  Massachusetts,  02720,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Michigan
      James Gilmore Jr. Treatment Center, Kalamazoo,  Michigan,  49408,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Oregon
      Willamette Family Treatment Services, Eugene,  Oregon,  97402,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

      Willamette Family Treatment Services-Men's & Co-ed, Eugene,  Oregon,  97408,  United States; Not yet recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

      Williamette Family Treatment Services, Buckley, Eugene,  Oregon,  97402,  United States; Not yet recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Rhode Island
      SSTAR of Rhode Island - North Kingstown, North Kingstown,  Rhode Island,  02852,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Washington
      Recovery Center King Co.-Kent Detox, Kent,  Washington,  98032,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

      Recovery Center King Co.-Seattle Detox, Seattle,  Washington,  98144,  United States; Recruiting
Laetitia Thompson, Ph.D.  303-315-2511    laetitia.thompson@uchsc.edu 

Study chairs or principal investigators

Robert Booth, Ph.D.,  Principal Investigator,  University of Colorado   

More Information

Study ID Numbers:  NIDA-CTN-0017-1
Record last reviewed:  January 2005
Last Updated:  March 8, 2005
Record first received:  January 27, 2005
ClinicalTrials.gov Identifier:  NCT00102349
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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September 4, 2008


Page Updated: November 22, 2004
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