Addressing Overdose Risk Among Recently Incarcerated People Living With HIV/AIDS

NCT ID: NCT03569592

Last Updated: 2020-08-05

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

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-22

Study Completion Date

2020-01-31

Brief Summary

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The overall objective of this study is to evaluate an educational overdose prevention intervention's effectiveness among incarcerated people living with HIV/AIDS, specifically within the context of other outcomes related to health and experiences after incarceration. Results will be used to develop tailored interventions to reduce overdose deaths among high-risk correctional populations.

The research has the following aims:

* Aim 1: Evaluate a pilot program to provide HIV+ inmates with 1:1 overdose prevention training while incarcerated;
* Aim 2: Identify the criminal justice, health, and HIV-related factors associated with overdose risk; and
* Aim 3: Describe the overdose risk experiences of HIV+ former inmates who use opioids after release.

Detailed Description

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The goal of this research is to establish best practices to address overdose risk in people exiting incarceration, people living with HIV/AIDS (PLWHA), and both populations simultaneously. This contribution is important because this evidence has applications for correctional facilities and HIV clinical practice throughout the United States. The contributions of the proposed pilot study are: to provide evidence on the effectiveness of a targeted intervention on these two high-risk groups, generate exploratory data on predictors of overdose risk specific to HIV status and recent incarceration, and provide context about overdose risk and responses to witnessed overdoses in the first month after release.

In this study, incarcerated PLWHA in the Philadelphia Department of Prisons will be offered overdose training while incarcerated and naloxone (Narcan) at release. Study participants will be given a pre-test on overdose knowledge and attitudes and receive the overdose prevention intervention. Those who are still incarcerated one month later will receive a post-test on overdose knowledge and attitudes. Approximately one month after study participants are released from jail, they will be given a one-month follow-up survey that assesses: overdose knowledge and attitudes (post-test 2), information on personal or witnessed overdoses since release, health and post-incarceration related information, and characteristics of drug use since release. Approximately 20 study participants will participate in a semi-structured interview 4-6 weeks after their release on their experiences with the overdose prevention intervention.

Conditions

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Drug Overdose Accidental

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Incarcerated people living with HIV/AIDS will be given a brief training on overdose prevention and be given naloxone at discharge from jail.
Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Overdose Prevention Intervention

The experimental group will receive a brief overdose prevention education intervention and be issues naloxone upon discharge from jail.

Group Type EXPERIMENTAL

Overdose Prevention Intervention

Intervention Type BEHAVIORAL

Evaluate an overdose prevention education with incarcerated people living with HIV/AIDS.

Interventions

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Overdose Prevention Intervention

Evaluate an overdose prevention education with incarcerated people living with HIV/AIDS.

Intervention Type BEHAVIORAL

Other Intervention Names

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Addressing Overdose Risk among Recently Incarcerated People Living with HIV/AIDS

Eligibility Criteria

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Inclusion Criteria

* HIV-positive
* Age 18 and over
* Speaks English
* plans to live in Philadelphia area after release

Exclusion Criteria

* More than 10 months remaining on a sentence or release date unknown
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Drexel University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Drexel University

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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1704005362

Identifier Type: -

Identifier Source: org_study_id

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