Evidence map›Paper›PMID 41027703›Full record

ArticleBMJ open2025

MINMON-J: a hybrid implementation pilot study evaluating a low-barrier hepatitis C treatment model in a jail setting.

Justin Berk, Emily S Fu, Matthew Murphy, Matthew J Akiyama, Mark Sulkowski, Josiah D Rich, Hannah Elizabeth Frank

Registry-linked trialAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06953479 (MINMON-J), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06953479 phase4recruitingnot on this map

MINMON-J: An Effectiveness Implementation Pilot Study Evaluating a Low-barrier Hepatitis C Treatment Model in a Jail Setting

TypeinterventionalSponsorLifespanRan2025 to 2027Enrolled40ConditionsHEPATITIS C (HCV), Incarceration, Injection Drug Use, Implementation ScienceArmsSofosbuvir / Velpatasvir Oral Tablet [Epclusa], Community Health Worker
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Justin BerkBrown University Warren Alpert Medical School, Providence, Rhode Island, USA justin_berk@brown.edu.
Emily S FuDepartment of Psychiatry and Human Behavior, Brown University Warren Alpert Medical School, Providence, Rhode Island, USA.
Matthew MurphyBrown University Warren Alpert Medical School, Providence, Rhode Island, USA.
Matthew J AkiyamaAlbert Einstein College of Medicine, New York, New York, USA.
Mark SulkowskiDivision of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Josiah D RichBrown University Warren Alpert Medical School, Providence, Rhode Island, USA.
Hannah Elizabeth FrankDepartment of Psychiatry and Human Behavior, Brown University Warren Alpert Medical School, Providence, Rhode Island, USA.

Funding

Project 4: Neonatal Abstinence Syndrome (NAS): Fetus to First YearsP20GM125507 · NIGMS · RHODE ISLAND HOSPITAL · PI JOSIAH D RICH · 2018 to 2026
$23.4M
Injectable Extended-Release Buprenorphine (XR-B) in a Correctional Setting: A Pilot Randomized Controlled TrialK23DA055695 · NIDA · RHODE ISLAND HOSPITAL · PI Justin Berk · 2022 to 2026
$1.0M
An intervention to improve HIV pre-exposure prophylaxis initiation, adherence and linkage to care for recently incarcerated men who inject drugs.K23DA054003 · NIDA · RHODE ISLAND HOSPITAL · PI Matthew Murphy · 2022 to 2026
$977k
Implementing a Low-Threshold Hepatitis C Treatment in a Jail SettingR34DA061732 · NIDA · RHODE ISLAND HOSPITAL · PI Justin Berk · 2024 to 2026
$723k
NIDA NIH HHS K23 DA054003NIDA NIH HHS K23 DA055695NIDA NIH HHS R34 DA061732NIGMS NIH HHS P20 GM125507
6 · The paper itself

Abstract

introductionHepatitis C virus (HCV) remains a leading cause of infectious disease-related morbidity in the USA, disproportionately affecting people who inject drugs and people who are incarcerated. Despite the availability of highly effective, highly tolerated direct-acting antivirals, treatment uptake in jails remains limited due to short stays, unpredictable release dates and system-level barriers. The original MINMON trial demonstrated that a low barrier 'minimal monitoring"' model can achieve high cure rates in community settings. This study, MINMON-J, aims to adapt and evaluate a modified version of the MINMON model for use in a jail setting, addressing the urgent need for scalable, low-barrier treatment approaches among justice-involved individuals. METHODS AND ANALYSIS: MINMON-J is a single-arm, hybrid effectiveness-implementation pilot study protocol planned to recruit at the Rhode Island Department of Corrections. 40 people who are incarcerated with positive HCV RNA, who are treatment-naïve, without cirrhosis and awaiting trial, will receive 12 weeks of sofosbuvir/velpatasvir with no required lab monitoring during treatment. If released before treatment completion, participants will receive their remaining medication at discharge. Community health workers will provide post-release support. Mixed-methods evaluation will be guided by the Reach, Effectiveness, Adoption, Implementation and Maintenance/Practical, Robust Implementation and Sustainability Model framework. Primary outcomes include feasibility, acceptability and adherence. Data will be collected through administrative records, surveys (Acceptability of Intervention Measure, Feasibility of Intervention Measure, Brief Adherence Rating Scale) and qualitative interviews with participants and other relevant parties. This study was reviewed and approved by the Brown University Health Institutional Review Board (2240400) and the Rhode Island Department of Corrections Medical Research Advisory Group. ETHICS AND DISSEMINATION: This study was reviewed and approved by the Brown University Health Institutional Review Board (2240400) and the Rhode Island Department of Corrections (RIDOC) Medical Research Advisory Group. All participants will provide written informed consent prior to enrolment. People who are incarcerated will be assured that participation is voluntary, will not impact their clinical care and that they may withdraw at any time without penalty. Study procedures follow ethical principles outlined in the Declaration of Helsinki and comply with federal regulations regarding research involving vulnerable populations.Dissemination of findings will include peer-reviewed publications and presentations at national conferences focused on infectious diseases, implementation science and/or correctional health. Lay summaries will be shared with RIDOC leadership and community partners. De-identified data and associated metadata may be archived in a publicly accessible repository in accordance with National Institutes of Health data sharing policies, contingent on final institutional review board approval and participant protections. TRIAL REGISTRATION NUMBER: NCT06953479.

Indexed as

Antiviral AgentsCarbamatesHepatitis CHepatitis C, ChronicJailsPrisonersSofosbuvirAdultBenzimidazolesBenzopyransFemaleHeterocyclic Compounds, 4 or More RingsHumansMalePilot ProjectsPrisonsAntiviral AgentsBenzimidazolesBenzopyransCarbamatesHeterocyclic Compounds, 4 or More RingsSofosbuvirvelpatasvirClinical TrialFeasibility StudiesHealth ServicesPatient NavigationPUBLIC HEALTH

Identifiers

PMID41027703
PMCPMC12506189

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.