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HIV and HCV Intervention In Drug Treatment Settings - 1

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ClinicalTrials.gov Identifier: NCT00102349
Recruitment Status : Completed
First Posted : January 28, 2005
Last Update Posted : January 12, 2017
Sponsor:
Collaborator:
Oregon Health and Science University
Information provided by:
National Institute on Drug Abuse (NIDA)

Study Description
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
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 or disease Intervention/treatment Phase
Behavior Therapy Behavioral: Behavior Therapy Phase 3

Study Design
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Study Type : Interventional  (Clinical Trial)
Enrollment : 706 participants
Primary Purpose: Prevention
Official Title: HIV and HCV Intervention in Drug Treatment Settings
Study Start Date : November 2004
Actual Primary Completion Date : February 2006
Actual Study Completion Date : February 2006

Resource links provided by the National Library of Medicine

MedlinePlus related topics: HIV/AIDS
U.S. FDA Resources

Arms and Interventions
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Outcome Measures
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Primary Outcome Measures :
  1. HIV/HCV injection risk behaviors

Eligibility Criteria
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 99 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
Volunteers will be IV drug users already enrolled in drug detoxification treatment.
Contacts and Locations
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00102349


Locations
United States, Colorado
Denver Health & Hosp Authority
Denver, Colorado, United States, 80204 4507
Island Grove RTC
Greeley, Colorado, United States, 80631
United States, Massachusetts
SSTAR (Stanley St. Treatment & Resources, Inc)
Fall River, Massachusetts, United States, 02720
United States, Michigan
James Gilmore Jr. Treatment Center
Kalamazoo, Michigan, United States, 49408
United States, Oregon
Willamette Family Treatment Services
Eugene, Oregon, United States, 97402
United States, Rhode Island
SSTAR of Rhode Island - North Kingstown
North Kingstown, Rhode Island, United States, 02852
United States, Washington
Recovery Center King Co.-Kent Detox
Kent, Washington, United States, 98032
Recovery Center King Co.-Seattle Detox
Seattle, Washington, United States, 98144
Sponsors and Collaborators
University of Colorado, Denver
Oregon Health and Science University
Investigators
Principal Investigator: Robert Booth, Ph.D. University of Colorado, Denver
More Information
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party: Robert Booth, Ph.D., University of Colorado at Denver
ClinicalTrials.gov Identifier: NCT00102349     History of Changes
Other Study ID Numbers: NIDA-CTN-0017-1
First Posted: January 28, 2005    Key Record Dates
Last Update Posted: January 12, 2017
Last Verified: October 2016

Keywords provided by National Institute on Drug Abuse (NIDA):
behavioral intervention