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TYRO Couples Project Study

NCT05267236 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 820

Last updated 2025-09-19

Study results available
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Summary

This study uses an RCT design with repeated measures to test the impact of two different delivery formats for the TYRO Couples curriculum. Eligible study participants are males or females who are at least 18 years of age and within 9 months of release from incarceration. Incarcerated participants randomly assigned to the treatment group receive the TYRO Couples curriculum in-person, whereas those assigned to the comparison group experience an on-demand format. Study results that show no discernable differences in outcomes between groups will make it easier to serve more participants because service delivery formats can accommodate different life circumstances and preferences.

Conditions

  • Couples

Interventions

OTHER

Intervention #1: Treatment Group Receiving On-Demand TYRO Services

Treatment group participants receive TYRO Couples curriculum in an on-demand format that is delivered in five 2-hour weekly sessions for a total of 10 hours.

OTHER

Intervention #2: Control Group Receiving In-Person TYRO Services

Control group participants receive TYRO Couples curriculum in a live format (virtual or in-person) that is delivered in five 2-hour weekly sessions for a total of 10 hours.

Sponsors & Collaborators

  • The RIDGE Project

    collaborator UNKNOWN

  • Midwest Evaluation & Research

    lead OTHER

Principal Investigators

  • Matt D Shepherd, PhD · Midwest Evaluation & Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-04-11
Primary Completion
2024-11-30
Completion
2025-08-15

Countries

  • United States

Study Locations

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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 NCT05267236 on ClinicalTrials.gov