Long-acting Naltrexone for Pre-release Prisoners

Long-acting Naltrexone for Pre-release Prisoners: A Randomized Trial of Mobile Treatment

This proposed five-year study will focus on whether the addition of providing XR-NTX treatment at a patients' place of residence will increase adherence and thus efficacy of the medication.Following initial screening, informed consent, and medical examination, pre-release prisoners at each facility will be block randomized (N=240) within gender to either: Condition 1. XR-NTX-OTx (n=120): One injection of XR-NTX in prison, followed by six monthly injections post-release in the community at an opioid treatment program; or Condition 2. XR-NTX+MMTx (n=120): One injection of XR-NTX in prison, followed by six monthly injections post-release in the community at the patient's place of residence.

Study Overview

• Status: Completed
• Conditions: Opiate Addiction
• Intervention / Treatment: Drug: XR-NTX; Other: place of residence; Other: opioid treatment program

Detailed Description

Disorders involving opioid use are a severe problem among jail and prison inmates. Inmates in the US, Canada, Australia, and many European and Asian nations have disproportionately higher rates of opioid use disorders than their general populations. Scarce resources are provided for corrections-based substance use treatment in many nations, and many inmates with OUDs remain untreated. The use of long-acting, injectable naltrexone (XR-NTX) may be a promising form of treatment for pre-release prisoners. Naltrexone blocks the intoxicating and reinforcing effects of opioids, but has no opioid-like effects. This proposed five-year study will focus on whether the addition of providing XR-NTX treatment at a patients' place of residence will increase adherence and thus efficacy of the medication. Project implementation will occur at five pre-release prisons under the jurisdiction of the Maryland Department of Public Safety and Correctional Services (MDPSCS): 1) Metropolitan Transition Center (MTC) for men; 2) Baltimore Pre-Release Unit (BPRU) for men; 3) Jessup Pre-Release Unit (JPRU) for men; 4) Baltimore City Correctional Center (BCCC) and 5) Maryland Correctional Institution (MCI) for Women. Following initial screening, informed consent, and medical examination, pre-release prisoners at each facility will be block randomized (N=240) within gender to either: Condition 1. XR-NTX-OTx (n=120): One injection of XR-NTX in prison, followed by six monthly injections post-release in the community at an opioid treatment program; or Condition 2. XR-NTX+MMTx (n=120): One injection of XR-NTX in prison, followed by six monthly injections post-release in the community at the patient's place of residence. All participants will be confirmed opiate-free by urine test and negative naloxone and oral naltrexone tests, and evaluated monthly for seven months and 12 months after release from prison. The proposed study has two specific aims: Aim1. To compare the two study conditions in terms of: a) XR-NTX treatment adherence; b) opioid use; c) criminal activity; d) re-arrest; e) re-incarceration; and f) HIV risk-behaviors (i. needle use; ii. risky sexual behaviors). Aim 2. To determine if the number of months of post-release XR-NTX treatment is related to outcome (a-f above), and if so, is there a point at which XR-NTX v. Non-XR-NTX equilibrates? This would help determine the number of injections, important because of XR-NTX cost. Many individuals in the criminal justice system drop out of treatment and therefore increasing ways to improve adherence by attempting to: 1) expand capacity; and 2) implement access by providing treatment at their place of residence may positively impact outcomes.

• Study Type: Interventional
• Enrollment (Estimated): 240
• Phase: Phase 3

Contacts and Locations

Study Locations

• United States
  • Maryland
    • Towson, Maryland, United States, 21286
      • Maryland Department of Public Safety and Correctional Services

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Adult male or female inmate at MTC, BPRU, JPRU, BCCC, or MCIW and be eligible for release within 30 days
• History of opiate disorder [meeting DSM-V criteria of dependence at the time of incarceration]
• Suitability for XR-NTX treatment as determined by medical evaluation
• Currently opioid-free by history, with negative urine for all opioids and no signs of opiate withdrawal
• Willingness to enroll in XR-NTX treatment in prison [not currently in or planning to pursue agonist (methadone, buprenorphine) treatment at release]
• Planning to live in Baltimore City or County.
• Inmates not meeting the opioid-dependence criterion will be eligible if they were treated in an opioid agonist treatment program during the year before incarceration

Exclusion Criteria:

• Liver function test levels greater than three times normal
• Active medical illness that may make participation hazardous (e.g., unstable diabetes, heart disease). Adequately treated medical conditions are acceptable
• Untreated psychiatric disorder that may make participation hazardous (e.g., untreated psychosis, bipolar disorder with mania). Adequately treated psychiatric disorders and appropriate psychotropic medications will be allowed
• History of allergic reaction to XR-NTX
• Current chronic pain diagnosis for which opioids are prescribed
• Creatinine above normal limits
• Pregnancy (for women)
• Breast-feeding (for women)
• Suicidal ideation (within the past 6-months)
• Body Mass Index (BMI) > 40
• Unadjudicated charges that may result in transfer to another facility and/or additional prison time.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Vivitrol at place of residence; One injection of long-acting naltrexone (XR-NTX) in prison, followed by 6 monthly injections post-release at the participants's place of residence utilizing mobile medical treatment	Drug: XR-NTX; Vivitrol; Other Names: long-acting naltrexone; Other: place of residence; One injection of XR-NTX in prison, followed by 6 monthly injections post-release at place of residence; Other Names: residence
Active Comparator: Vivitrol at opioid treatment program; One injection of long-acting naltrexone (XR-NTX) in prison, followed by 6 monthly injections post-release at a community opioid treatment program.	Drug: XR-NTX; Vivitrol; Other Names: long-acting naltrexone; Other: opioid treatment program; One injection of XR-NTX in prison, followed by 6 monthly injections post-release at a community opioid treatment program; Other Names: OTP

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
treatment adherence	XR-NTX+ MMTx vs. XR-NTX-OTx following release from prison	six months
Any illicit opioid used	defined as continuous counts of days and urine toxicologies for heroin or other illicit opioid	1,2,3,4,5,6,7 and 12-months following release from prison
re-arrest	Re-arrest will be assessed using self-report on the Arrests and Days Incarcerated form and from Official Records received from the Maryland Department of Public Safety and Correctional Services	12-months following release from prison
re-incarceration	Re-incarceration will be assessed using self-report on the Arrests and Days Incarcerated form and from Official Records received from the Maryland Department of Public Safety and Correctional Services	12-months following release from prison
criminal activity	Self-reported crime days will be defined as continuous counts of days collected from the Addiction Severity Index and Time Line Follow-Back	1,2,3,4,5,6,7 and 12-months following release from prison
Injection drug use and HIV sexual risk factors	Injection drug use and HIV sexual risk factors will be measured using the Risk Assessment Battery.	6 and 12-months following release from prison

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Treatment Group Equilibration	time point at which the trajectories for use in the two treatment groups cross	6 and 12-months following release from prison

Collaborators and Investigators

• Sponsor: Friends Research Institute, Inc.
• Collaborators: National Institute on Drug Abuse (NIDA)
• Investigators: Principal Investigator: Michael S Gordon, DPA, Friends Research Institute, Inc.

Publications and helpful links

General Publications

• Gordon MS, Vocci FJ, Fitzgerald TT, O'Grady KE, O'Brien CP. Extended-release naltrexone for pre-release prisoners: A randomized trial of medical mobile treatment. Contemp Clin Trials. 2017 Feb;53:130-136. doi: 10.1016/j.cct.2016.12.015. Epub 2016 Dec 20.
• Kornor H, Lobmaier PPK, Kunoe N. Sustained-release naltrexone for opioid dependence. Cochrane Database Syst Rev. 2025 May 9;5(5):CD006140. doi: 10.1002/14651858.CD006140.pub3.

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2017
• Primary Completion (Actual): February 10, 2025
• Study Completion (Actual): January 1, 2026

Study Registration Dates

• First Submitted: August 8, 2016
• First Submitted That Met QC Criteria: August 10, 2016
• First Posted (Estimated): August 15, 2016

Study Record Updates

• Last Update Posted (Actual): February 3, 2026
• Last Update Submitted That Met QC Criteria: January 30, 2026
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Narcotic-Related Disorders; Mental Disorders; Substance-Related Disorders; Chemically-Induced Disorders; Opioid-Related Disorders; Public Health; Environment and Public Health; Population Characteristics; Demography; Epidemiologic Measurements; Residence Characteristics
• Other Study ID Numbers: FriendsResearch; R01DA040636 (U.S. NIH Grant/Contract)