HIV, Buprenorphine, and the Criminal Justice System (STRIDE2)

NCT ID: NCT03583138

Last Updated: 2020-05-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

159 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-06-23

Study Completion Date

2017-06-30

Brief Summary

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STRIDE2 is a longitudinal, non-randomized study of individuals living with HIV who are dependent on opioids. This study is funded by the National Institute on Drug Abuse (R01DA030768, Altice, PI; Taxman \& Lawson, Co-PIs) and is being conducted by George Mason University, Yale University, and Howard University.

Detailed Description

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STRIDE2 will assist in identifying and monitoring individuals' HIV risk behaviors and provide resources to seek treatment for their HIV care and substance use. The goal of STRIDE2 is to examine if there are differences in HIV, drug use, and other outcomes between individuals receiving treatment versus individuals actively using, not actively using and not in treatment, and individuals on Methadone, Suboxone, or in some other treatment.

Conditions

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Human Immunodeficiency Virus Acquired Immunodeficiency Syndrome Opiate Addiction Drug Dependence

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Buprenorphine

Participants are eligible for the study if they are 18 years of age or older, HIV+, meet DSM-IV criteria for opioid dependence, have health insurance accepted at Lab Corp, are able to read and understand English, and live in Washington, DC and plan to remain in DC. The intervention is to provide buprenorphine for 12 months for those who are interested in receiving it.

buprenorphine

Intervention Type DRUG

To provide buprenorphine for 12 months for those who are interested in receiving it.

No buprenorphine

No buprenorphine

No interventions assigned to this group

Interventions

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buprenorphine

To provide buprenorphine for 12 months for those who are interested in receiving it.

Intervention Type DRUG

Other Intervention Names

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Suboxone

Eligibility Criteria

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Inclusion Criteria

1. HIV+, confirmed by rapid HIV test
2. Meet DSM-IV criteria for opioid dependence
3. 18 years or older
4. Have health insurance that is accepted at Lab Corp.

Exclusion Criteria

1. Are \<18 years old;
2. Are HIV negative;
3. Are Unable to communicate in English;
4. Are not able to provide informed consent;
5. Do not meet DSM-IV criteria for opioid dependence;
6. Plan to leave the DC area
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

George Mason University

OTHER

Sponsor Role collaborator

Howard University

OTHER

Sponsor Role collaborator

Yale University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Fredrick Altice, MD

Role: PRINCIPAL_INVESTIGATOR

Yale University School of Medicine/AIDS Program

Faye Taxman, PhD

Role: PRINCIPAL_INVESTIGATOR

George Mason University

William Lawson, MD

Role: PRINCIPAL_INVESTIGATOR

Howard University

Locations

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Howard University

Washington D.C., District of Columbia, United States

Site Status

Countries

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United States

Other Identifiers

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R01DA030768

Identifier Type: NIH

Identifier Source: secondary_id

View Link

1011007631b

Identifier Type: -

Identifier Source: org_study_id

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