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A Mobile Text Approach to Measurement and Feedback for Wraparound Care Coordination

NCT07300930 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 216

Last updated 2025-12-24

No results posted yet for this study

Summary

This SBIR Phase II proposal will fully develop and test the acceptability, feasibility, and efficacy of a novel measurement and feedback system, SMART-Wrap, tailored to Wraparound service model (WSM) for youth with serious emotional disorders (SED). SMART-Wrap will be a feasible, cost-efficient, and scalable software system to meet the pressing public health need for measurement-based care in care coordination for youth behavioral health. Results from pilot testing will determine SMART-Wrap's feasibility, usability, and efficacy in improving care quality and family outcomes, in addition to preparing the product for commercialization.

Conditions

  • Mental Health Services
  • Mobile Technologies
  • Technology Development

Interventions

BEHAVIORAL

SMARTwrap

An SMS-based intervention to facilitate regular, repeated evaluation of intermediate outcomes through self-report assessments for youth under Wraparound service model (WSM) care.

Sponsors & Collaborators

  • University of Washington

    collaborator OTHER

  • National Institute of Mental Health (NIMH)

    collaborator NIH

  • 3-C Institute for Social Development

    lead INDUSTRY

Principal Investigators

  • Melissa DeRosier, PhD · 3C Institute

  • Eric Bruns, PhD · University of Washington

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-01
Primary Completion
2026-12-31
Completion
2027-02-28

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT07300930 on ClinicalTrials.gov