Re-entry XR-NTX for Rural Individuals With Opioid Use Disorder

NCT ID: NCT03447743

Last Updated: 2023-03-27

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

9 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-09-11

Study Completion Date

2022-03-09

Brief Summary

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The overall aim of this R34 proposal is to examine the feasibility, acceptability, and short-term outcomes associated with an innovative service delivery model to increase adherence to extended-release naltrexone (XR-NTX) during the transition from jail to the community for rural individuals with opioid use disorder (OUD). The significance of this study is grounded in the public health emergency associated with the opioid epidemic in rural Appalachia, the increased vulnerability of rural individuals with OUD, and the dearth of available and accessible evidence-based treatment in the region. This study has potential to make a significant contribution to the OUD treatment field by advancing knowledge on innovative service delivery models to increase access to evidence-based treatment to reduce the prevalence of opioid use disorders and related health disparities among hard-to-reach, high-risk, underserved populations.

Detailed Description

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The overall aim of this R34 proposal is to examine the feasibility, acceptability, and short-term outcomes associated with an innovative service delivery model to increase adherence to extended-release naltrexone (XR-NTX) during the transition from jail to the community for rural individuals with opioid use disorder (OUD). The significance of this study is grounded in the public health emergency associated with the opioid epidemic in rural Appalachia, the increased vulnerability of rural individuals with OUD, and the dearth of available and accessible evidence-based treatment in the region. This R34 has potential to make a significant contribution to the OUD treatment field by advancing knowledge on innovative service delivery models to increase access to evidence-based treatment to reduce high-risk opioid use and related health disparities among hard-to-reach, high-risk, underserved populations. The study will be accomplished through two specific aims: (1) Adapt XR-NTX services for use in community supervision (P\&P) offices to increase adherence during re-entry from jail for rural individuals with OUD. (2) A small scale pilot will be conducted to examine feasibility, acceptability, and short-term outcomes of the adapted protocol on XR-NTX adherence and relapse to opioid use. Rural justice-involved individuals on community supervision with OUD will be invited to initiate XR-NTX and continue injections for up to three months in the community. If this study establishes feasibility of this innovative community-based treatment model for XR-NTX in a rural, underserved area, findings will be used to develop an R01 application to test the approach in a larger RCT during community re-entry from jail among high-risk rural individuals with OUD in Appalachia. The long-term goal of this research is to increase access to evidence-based treatment for OUD among high-risk, underserved populations.

Conditions

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Opioid Dependence

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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XR-NTX services as usual

Participants will receive on-going XR-NTX injections in a local community clinic

Group Type OTHER

XR-NTX community location

Intervention Type DRUG

XR-NTX will be administered at the local health care clinic

Interventions

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XR-NTX community location

XR-NTX will be administered at the local health care clinic

Intervention Type DRUG

Other Intervention Names

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Vivitrol

Eligibility Criteria

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Inclusion Criteria

* Meets criteria for opioid use disorder
* Anticipated release date within 30 days
* Opioid free
* Not currently in methadone or buprenorphine trial
* No serious medical or psychiatric condition
* Willingness to enroll in the trial

Exclusion Criteria

* Positive study pregnancy test
* Abnormal liver function tests (5X upper limits of normal)
* Chronic pain conditions that require opioid therapies
* Untreated medical or psychiatric disorder
* Suicidal ideation
* BMI \> 40
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Institute on Drug Abuse (NIDA)

NIH

Sponsor Role collaborator

Michele Staton

OTHER

Sponsor Role lead

Responsible Party

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Michele Staton

Associate Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Michele Staton, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Kentucky

Locations

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University of Kentucky

Lexington, Kentucky, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol and Informed Consent Form

View Document

Other Identifiers

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R34DA045856-01

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R34DA045856-01

Identifier Type: NIH

Identifier Source: org_study_id

View Link

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