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Juvenile Justice Translational Research on Interventions for Adolescents in the Legal System ((JJ-TRAILS))

22. Juli 2019 aktualisiert von: Michael L. Dennis, Ph.D., Chestnut Health Systems

Juvenile Justice Translational Research on Interventions for Adolescents in the Legal System: Multi-site Implementation Study

This is a multi site experiment to evaluate the impact of various strategies for increasing the use of evidence based screening, assessment and linkage to substance use treatment. All sites collect baseline data and receive a core intervention. Half are then randomly assigned to get an additional year of coaching to facilitate implementation.

Studienübersicht

Status

Abgeschlossen

Detaillierte Beschreibung

Background: The Juvenile Justice-Translational Research on Interventions for Adolescents in the Legal System (JJ-TRIALS) study is a cooperative implementation science initiative involving the National Institute on Drug Abuse, six Research Centers, a Coordinating Center, and Juvenile Justice Partners representing seven U.S. states. The pooling of resources across Centers enables a robust implementation study design involving 36 juvenile justice agencies and their behavioral health partner agencies, coproducing a study protocol that has potential to advance implementation science, meets the needs of all constituencies (funding agency, researchers, partners, study sites), and can be implemented with fidelity across the cooperative can be challenging.

Methods/design: The JJ-TRIALS primary study uses a head-to-head cluster randomized trial with a phased rollout to evaluate the differential effectiveness of two conditions (Core and Enhanced) in 36 sites located in 7 states. Core strategies for promoting change are compared to an Enhanced strategy that incorporate all core strategies plus active facilitation. Target outcomes include improvements in evidence-based screening, assessment, and linkage to substance use treatment.

Primary Research Questions:

  1. Does the Core and/or Enhanced Intervention reduce unmet need by increasing Cascade retention related to screening, assessment, treatment initiation, engagement and continuing care?
  2. Does the addition of the Enhanced Intervention components further increase the percentage of youth retained in the Cascade relative to the Core components?
  3. Does the addition of the Enhanced Intervention components improve service quality relative to Core sites?
  4. Do staff perceptions of the value of best practices increase over time, and are increases more pronounced in Enhanced sites?

Studientyp

Interventionell

Einschreibung (Tatsächlich)

839

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Georgia
      • Atlanta, Georgia, Vereinigte Staaten, 30322
        • Emory University
    • Illinois
      • Bloomington, Illinois, Vereinigte Staaten, 61701
        • Chestnut Health Systems
    • Kentucky
      • Lexington, Kentucky, Vereinigte Staaten, 40508
        • University of Kentucky
    • Maryland
      • Rockville, Maryland, Vereinigte Staaten, 20892
        • National Institute on Drug Abuse
    • Mississippi
      • Starkville, Mississippi, Vereinigte Staaten, 39759
        • Mississippi State University
    • New York
      • New York, New York, Vereinigte Staaten, 10032
        • Columbia University
    • Pennsylvania
      • Philadelphia, Pennsylvania, Vereinigte Staaten, 19122
        • Temple University
    • Texas
      • Fort Worth, Texas, Vereinigte Staaten, 76129
        • Texas Christian University

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Specific site inclusion criteria include: (a) ability to provide youth service records, (b) service to youth under community supervision, (c) access to treatment provider(s) if treatment is not provided directly by the JJ agency, (d) participation in requisite intervention training/activities,(e) minimum average case flow of 10 youth per month, (f) minimum of 10 staff per site, and (g) a senior JJ staff member who agrees to serve as site leader/liaison during the study. Study sites are geographically dispersed and were identified by state JJ agencies (and not selected for particular substance use or related BH service needs).

Youth inclusion criteria include: all youth entering the juvenile justice system during the period within the exception of those who are already in treatment at the time that they are referred to the juvenile justice agency.

Staff inclusion criteria include: all staff actively working with the youth under community supervision in the site with exclusion only of higher level administrative or regional staff over multiple units..

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Versorgungsforschung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Kein Eingriff: Control
During the Baseline Control data is collected in all 36 sites at the agency, staff, and youth level on the 6 months prior to the interventions in Arms 2 & 3 to document what practice was before the study.
Aktiver Komparator: Core

In the second phase (after baseline) all 36 sites receive a Core condition that includes five interventions: (1) JJ-TRIALS Orientation Meetings, (2) Needs Assessment, (3) Behavioral Health Training, (4) Site Feedback Report, (5) Goal Achievement Training, (6) Monthly Site Check-ins, and (7) Quarterly Reports. As part of Goal Achievement Training, sites receive assistance in using their Site Feedback Reports to select goals to meet their local needs. Sites are trained on using Data-Driven Decision Making (DDDM) to inform decisions (e.g., selecting a goal, monitoring progress) and enlisting DDDM templates and tools (developed as part of the project) to plan and implement proposed changes.

these principles to their improvement efforts during the implementation phase.

Andere Namen:
  • GAT, DDDM
Experimental: Enhanced
While the core intervention and DDDM are expected to facilitate change, organizations may need additional support to apply these principles to their improvement efforts during the implementation phase. In the third phase (after Core), 1/2 of the sites are randomly assigned to an Enhanced condition that provides continuing support for the use of DDDM tools by adding research staff facilitation of DDDM over a 12-month period and formalized Local Change Teams (LCTs) featuring representation from the JJ agency and a local BH provider, with meetings facilitated by research staff).
Andere Namen:
  • GAT, DDDM
Andere Namen:
  • DDDM, Facilitation

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Service Cascade: % Referred to Substance Use Treatment
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth referred to substance use treatment divided by the number of youth identified as need of substance use treatment.
120 weeks
Staff Perception: Value of Evidenced Based Substance Use Treatment
Zeitfenster: 120 weeks
Calculated from staff surveys at juvenile justice and substance use treatment agencies as the average staff ranking of the perceived "value" of using of evidence-based substance use treatment services.
120 weeks

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Service Cascade: % Screened for Substance Use Problems
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth "Screened" for substance use problems divided by the number of youth entering the juvenile justice system.
120 weeks
Service Cascade: % Clinically Assessed for Substance Use Problems
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth "Clinically Assessed" for substance use problems divided by the number of youth entering the juvenile justice system.
120 weeks
Service Cascade: % In Need of Substance Use Treatment
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth identified (via screening, clinical assessment or other sources) as "In Need of Substance Use Treatment" divided by the number of youth entering the juvenile justice system.
120 weeks
Service Cascade: % Initiating Substance Use Treatment
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth "Initiating" Substance Use Treatment within 90 days of referral" divided by the number referred to treatment from the juvenile justice system.
120 weeks
Service Cascade: % Engaged in Substance Use Treatment
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the number of youth "Engaged" in Substance Use Treatment for 6 weeks or more weeks divided by the number initiating treatment.
120 weeks
Service Cascade: % With Substance Use Treatment Continuing Care
Zeitfenster: 120 weeks
number of youth "Continuing" to receive substance use treatment services forCalculated from juvenile justice and substance use treatment agency records as the 90 days or more divided by the number initiating treatment.
120 weeks
Service Quality: Timing of Screening or Clinical Assessment
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the mean days from entry into the justice system to the first of screening or clinical assessment for substance use problems.
120 weeks
Service Quality: Timing of Substance Use Treatment Initiation
Zeitfenster: 120 weeks
Calculated from juvenile justice and substance use treatment agency records as the mean days from referral to and initiation of substance use treatment.
120 weeks
Service Quality: Number of Evidence Based Practices
Zeitfenster: 120 Weeks
Based on agency surveys and youth records from juvenile justice and substance use treatment agencies, the number of steps using 1 or more evidenced based practices in each of the following steps along the service cascade: screening, clinical assessment, referral, substance use treatment.
120 Weeks
Staff Perception: Value of Evidenced Based Screening
Zeitfenster: 120 weeks
Calculated from staff surveys at juvenile justice and substance use treatment agencies as the average staff ranking of the perceived "value" of using of evidence-based screening.
120 weeks
Staff Perception: Value of Evidenced Based Clinical Assessment
Zeitfenster: 120 weeks
Calculated from staff surveys at juvenile justice and substance use treatment agencies as the average staff ranking of the perceived "value" of using of evidence-based clinical assessment.
120 weeks
Staff Perception: Value of Evidenced Based Substance Use Prevention
Zeitfenster: 120 weeks
Calculated from staff surveys at juvenile justice and substance use treatment agencies as the average staff ranking of the perceived "value" of using of evidence-based substance use prevention.
120 weeks
Staff Perception: Value of Evidenced Based HIV Risk Prevention
Zeitfenster: 120 weeks
Calculated from staff surveys at juvenile justice and substance use treatment agencies as the average staff ranking of the perceived "value" of using of evidence-based HIV Risk prevention.
120 weeks

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Christy K Scott, Ph.D., Chestnut Health Systems
  • Hauptermittler: Danica K Knight, Ph.D., Texas Christian University
  • Hauptermittler: Michael L Dennis, Ph.D., Chestnut Health Systems
  • Hauptermittler: Tisha R Wiley, Ph.D., National Institute on Drug Abuse (NIDA)
  • Hauptermittler: Gail A Wasserman, Ph.D., Columbia University
  • Hauptermittler: Ralph DiClemente, Ph.D., Emory University
  • Hauptermittler: Gene H Brody, Ph.D., Emory University
  • Hauptermittler: Angela A Robertson, Ph.D., Mississippi State University
  • Hauptermittler: Steven R Belenko, Ph.D., Temple University
  • Hauptermittler: Carl G Leukefeld, Ph.D., University of Kentucky

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Nützliche Links

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

1. Juli 2013

Primärer Abschluss (Tatsächlich)

31. Januar 2019

Studienabschluss (Tatsächlich)

30. Juni 2019

Studienanmeldedaten

Zuerst eingereicht

22. Januar 2016

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

29. Januar 2016

Zuerst gepostet (Schätzen)

3. Februar 2016

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

23. Juli 2019

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

22. Juli 2019

Zuletzt verifiziert

1. Juli 2019

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • JJ-TRIALS
  • U01DA036221 (US NIH Stipendium/Vertrag)
  • U01DA036226 (US NIH Stipendium/Vertrag)
  • U01DA036233 (US NIH Stipendium/Vertrag)
  • U01DA036176 (US NIH Stipendium/Vertrag)
  • U01DA036225 (US NIH Stipendium/Vertrag)
  • U01DA036224 (US NIH Stipendium/Vertrag)
  • U01DA036158 (US NIH Stipendium/Vertrag)

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

The coordinating center is charged with creating de-identified versions of agency, staff and client level service data available at the end of the study.

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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