Increasing Caregiver Engagement in Juvenile Drug Courts

NCT03051997 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2025-12-08

Study results available
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Summary

The purpose of this study is to test a prize-based contingency management intervention for increasing caregiver engagement in juvenile drug court and adolescent drug treatment, and for achieving the ultimate outcomes of reduced substance use and delinquent behavior among drug court-involved youth.

Conditions

Interventions

BEHAVIORAL

Caregiver Contingency Management + Usual Drug Court Treatment

In addition to receiving JDC treatment as usual described below, caregiver participants will receive prize draws for engaging in activities consistent with their adolescents' successful completion of the JDC program during the time the youth is actively involved in JDC and substance abuse treatment. Specific activities that may be reinforced include: attendance at drug court hearings; accompanying the youth to probation meetings; participating in home visits; attendance at the youth's drug treatment sessions; attendance at mental health provider meetings; attending groups for parents of youth with substance abuse issues; and completing other verifiable treatment-related activities. All activities will meet the goals of (directly or indirectly) enhancing caregiver participation in the JDC and/or treatment process. Caregivers will receive escalating chances for tangible reinforcers each week for completing up to 3 of the activities agreed upon by the caregiver and the therapist.

BEHAVIORAL

Usual Drug Court Treatment

Standard outpatient substance abuse treatment services that a young person would receive while participating in JDC.

Sponsors & Collaborators

  • National Institute on Minority Health and Health Disparities (NIMHD)

    collaborator NIH
  • Wayne State University

    collaborator OTHER
  • Alliant International University

    collaborator OTHER
  • Baylor University

    collaborator OTHER
  • Medical University of South Carolina

    lead OTHER

Principal Investigators

  • Phillippe Cunningham, Ph.D. · Medical University of South Carolina

  • David Ledgerwood, Ph.D. · Wayne State University

  • Stacy Ryan, Ph.D. · The University of Texas Health Science Center at San Antonio

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-13
Primary Completion
2023-12-12
Completion
2024-12-12

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03051997 on ClinicalTrials.gov