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Linking Individuals Needing Care for Substance Use Disorders to Peer Coaches & Across INcarceration Settings (LINCS UP & IN)

13 août 2026 mis à jour par: Joseph Carpenter, Emory University

The goal of this study is to learn whether a virtual peer recovery coach (PRC) intervention can improve engagement in addiction treatment among incarcerated adults with substance use disorders.

The main questions it aims to answer are:

  • Does the PRC intervention increase engagement with at least one recovery resource at 30 and 90 days?
  • Does it improve secondary outcomes such as substance use, recovery capital, overdose events, and recidivism?

Researchers will compare Treatment-as-Usual with the PRC telehealth intervention to see if PRC support improves engagement in addiction care.

Participants will:

  • Complete baseline and follow-up assessments
  • Receive either Treatment-as-Usual or a virtual PRC session focused on motivational interviewing and linkage to recovery resources

Aperçu de l'étude

Description détaillée

This study evaluates a virtual peer recovery coach (PRC) intervention designed to support adults with substance use disorders during incarceration and the transition back to the community. The trial is conducted across multiple jail facilities in Metro Atlanta, where individuals experience high rates of substance use disorders and limited access to treatment services. Peer recovery coaches-individuals with lived experience who are trained in motivational interviewing and linkage to care-have demonstrated benefit in healthcare settings, but their effectiveness within jail environments has not been rigorously tested.

The intervention adapts an existing virtual PRC model for use in jail settings. PRCs meet with participants through a secure telehealth platform and provide individualized support focused on motivation, readiness for change, and connection to recovery resources. The model is designed to be scalable, flexible, and responsive to the needs of individuals with diverse substance use profiles, including those for whom no FDA-approved medications exist.

The study uses a phased implementation approach in which participating jail sites transition from usual care to the PRC intervention over time. This structure allows the program to be integrated into each facility's workflow while enabling evaluation of the intervention's impact. Participants are followed for one year to assess engagement with recovery resources and other indicators of health, stability, and community reintegration.

The findings will inform whether virtual PRC services can be effectively delivered in jail settings and whether they improve connection to treatment and recovery supports during a period of heightened vulnerability. Results may guide future implementation of peer-based models in correctional systems and other high-risk environments.

Type d'étude

Interventionnel

Inscription (Estimé)

550

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Joseph Carpenter, MD
  • Numéro de téléphone: 404-778-5975
  • E-mail: jecarpe@emory.edu

Sauvegarde des contacts de l'étude

Lieux d'étude

    • Georgia
      • Atlanta, Georgia, États-Unis, 30303
        • Recrutement
        • Atlanta City Detention Center
      • Atlanta, Georgia, États-Unis, 30318
        • Recrutement
        • Fulton County Jail
      • Decatur, Georgia, États-Unis, 30032
        • Recrutement
        • Dekalb County Jail

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Incarcerated at participating jail
  • Able to speak and understand English
  • Score of 3 or greater - "moderate level", "substantial level", or "severe level" of problems related to drug abuse - on DAST-10.
  • Willing to follow study procedures and complete research follow-up calls
  • Have at least two reliable contact numbers, e.g. participant and one or more relatives or close friends

Exclusion Criteria:

  • Cognitive impairment (inability to comprehend the informed consent document as assessed by study staff during enrollment)
  • Prior participation in the study
  • Awaiting transfer to prison or jail outside the state of Georgia

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Soins de soutien
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: PRC group
Participants meet virtually with a trained peer recovery coach using a secure telehealth platform. PRCs use motivational interviewing, assess readiness to change, and provide individualized linkage to recovery resources. Support may include connection to medications for opioid use disorder, residential treatment, detoxification centers, harm reduction services, mutual support groups, sober living, or recovery community organizations. PRCs may also conduct post-release check-ins to support ongoing engagement.
A telehealth session with a peer recovery coach who provides motivational interviewing and tailored linkage to addiction treatment and recovery resources.
Comparateur actif: Standard of Care
Participants receive the jail's standard approach to substance use support. This includes a review of available community treatment and recovery resources consistent with existing facility practices. No peer recovery coach is involved, and no additional study-driven services are provided.
Participants are provided information about community-based addiction treatment and recovery resources as part of routine jail processes.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Engagement With at Least One Recovery Resource
Délai: 30 days and 90 days after enrollment

Engagement with at least one recovery resource, defined as:

  • Formal addiction treatment (visit with a physician, psychologist, or licensed substance use counselor; or ≥1 night in detoxification or residential treatment), or
  • Recovery Community Organization (RCO) participation (contact, intake, and participation in ≥1 evidence-based recovery activity), or
  • Harm reduction organization engagement. Engagement may occur during incarceration or in the community after release.
30 days and 90 days after enrollment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Days Receiving Medications for Substance Use Disorders
Délai: Baseline to 30 days, 90 days, 180 days, and 1 year
Number of days participants receive medications for opioid use disorder (MOUD), stimulant use disorder, or alcohol use disorder.
Baseline to 30 days, 90 days, 180 days, and 1 year
Recidivism and Justice Involvement
Délai: Baseline to 1 year
New arrests, bookings, or jail stays documented through participant report or administrative data.
Baseline to 1 year
Healthcare Utilization
Délai: Baseline to 1 year
Emergency department visits, hospitalizations, and other acute care encounters.
Baseline to 1 year
Recovery Capital (BARC-10)
Délai: Baseline, 30, 90, 180 days, and 1 year

Brief Assessment of Recovery Capital (BARC-10) A 10-item validated scale that measures a person's internal and external resources that support recovery from substance use. Items assess domains such as social support, coping skills, housing stability, and personal motivation.

  • Scores range from 10 to 60.
  • Higher scores indicate greater recovery capital and stronger readiness to sustain recovery.
Baseline, 30, 90, 180 days, and 1 year
Number of Peer Recovery Coach Contacts
Délai: Baseline to 30 days, 90 days, 180 days, and 1 year
Number of PRC interactions among participants assigned to the intervention arm.
Baseline to 30 days, 90 days, 180 days, and 1 year
Self-Reported Substance Use (TLFB)
Délai: Baseline, 30, 90, 180 days, and 1 year
Days of substance use in the past 30 days using the Timeline Follow-Back method. A structured calendar-based interview used to measure self-reported substance use over the past 30 days. Participants recall days of use using memory anchors (events, routines).
Baseline, 30, 90, 180 days, and 1 year
Fatal Overdose Events
Délai: Baseline through 1 year
Overdose events identified through participant report, medical records, or community partner data.
Baseline through 1 year
Nonfatal Overdose Events
Délai: Baseline through 1 year
Overdose events identified through participant report, medical records, or community partner data.
Baseline through 1 year
Housing status
Délai: Baseline, 30, 90, 180 days, and 1 year
Current housing status (stable, unstable, homeless)
Baseline, 30, 90, 180 days, and 1 year
Employment status
Délai: Baseline, 30, 90, 180 days, and 1 year
Employment status (full-time, part-time, unemployed)
Baseline, 30, 90, 180 days, and 1 year
Social connections and Isolation: PROMIS scale
Délai: Baseline, 30, 90, 180 days, and 1 year

A validated set of items assessing perceived social support, loneliness, and connectedness.

  • Generates T-scores standardized to the U.S. population (mean = 50, SD = 10).
  • Higher scores on Social Support = more support.
  • Used to evaluate social determinants of recovery.
Baseline, 30, 90, 180 days, and 1 year
All-Cause Mortality
Délai: Baseline through 1 year
Death from any cause, confirmed through vital records or the National Death Index.
Baseline through 1 year

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Joseph Carpenter, MD, Emory University

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 mars 2030

Achèvement de l'étude (Estimé)

1 mars 2030

Dates d'inscription aux études

Première soumission

22 avril 2026

Première soumission répondant aux critères de contrôle qualité

29 avril 2026

Première publication (Réel)

4 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

17 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

13 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 2025P012936
  • 1R01DA064519-01 (Subvention/contrat des NIH des États-Unis)

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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