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An Evaluation of Innovative Methods for Integrating Buprenorphine Opioid Treatment in HIV Primary Care Settings
The purpose of this study is to assess the feasibility, cost and effectiveness of interventions designed to integrate buprenorphine treatment for opioid dependence into HIV primary care in ten HIV care centers in the U.S.
Programs that integrate medical care and drug treatment have shown great promise in improving health and substance use related outcomes. The overlap in the epidemics of HIV (with its complex medical needs) and drug abuse makes HIV-infected drug users a population likely to benefit from the integration of primary care and drug treatment. The Drug Addiction Treatment Act of 2000 and the approval of buprenorphine for the office-based treatment of opioid addiction provide a new opportunity to integrate addiction treatment and medical care for people with HIV. Research has demonstrated the effectiveness of buprenorphine in reducing illicit drug use among opioid dependent people. However, little is known about implementing such programs in HIV care settings, their cost, what effect they have on the health outcomes and substance use behavior of PLWH/A, or their broader impact on providers, institutions, and local systems. Through this study, approximately 1,350 HIV-infected individuals who meet criteria for opioid dependence will be selected by eleven model demonstration projects located in ten HIV care centers across the U.S. Information on patients' drug use, HIV health status, service utilization, quality of life, and satisfaction with services as well as information about providers' practices and attitudes towards treating drug dependent patients will be collected through face-to-face interviews, audio computer-assisted self-interviewing, written surveys, and chart abstractions. These data will be used to help replicate effective programs that integrated HIV care and drug treatment and to improve the care of HIV-infected opioid dependent individuals. Comparisons: All eleven programs will compare a group of patients who receive integrated buprenorphine treatment and HIV care to a group of patients who receive an alternate intervention. However, the program designs and comparison group interventions vary across the sites and are locally determined. Some sites will implement randomized control designs, while others will use observational methods.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
El Rio Santa Cruz Neighborhood Health Center
Tucson, Arizona, United States
Organization to Achieve Solutions in Substance Abuse
Oakland, California, United States
University of California San Francisco
San Francisco, California, United States
Yale University School of Medicine AIDS Program
New Haven, Connecticut, United States
University of Miami School of Medicine
Miami, Florida, United States
The CORE Center
Chicago, Illinois, United States
Johns Hopkins University
Baltimore, Maryland, United States
Montefiore Medical Center
New York, New York, United States
Oregon Health & Science University
Portland, Oregon, United States
The Miriam Hospital
Providence, Rhode Island, United States
Start Date
August 1, 2005
Completion Date
December 1, 2008
Last Updated
March 27, 2007
1,350
Estimated participants
Buprenorphine
DRUG
Integrated HIV care and office-based opioid dependence treatment
BEHAVIORAL
Lead Sponsor
The New York Academy of Medicine
Collaborators
NCT04929028
NCT06694805
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04142047