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Clinical Trials in the USA / NCT07300930
Starting soon Not applicable

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

NCT07300930 · tracked via the Priya Life Science USA tracker
Sponsor
3-C Institute for Social Development
Phase
Not applicable
Started
2026-10-01
Last updated
2026-09-02

Condition(s) studied

Mental Health ServicesMobile TechnologiesTechnology Development

Investigational drug(s) / intervention(s)

SMARTwrap

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.

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.

Eligibility

Sex
ALL
Min age
8 Years
Max age
Healthy volunteers
No
Inclusion Criteria: Families * be youth with SED aged 8-17 or caregivers of youth with SED age 8-17 * have access to a mobile device * be English or Spanish speaking Exclusion Criteria: Families * To reduce heterogeneity and increase interpretability however, youth (approximately 10%) in foster care served by Wraparound provider organizations will be excluded. Inclusion Criteria: Care Teams * must agree to use SMART-Wrap over an 8-month period to participate * must include supervisors and care coordinators

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
3C Institute Durham North Carolina
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07300930 on ClinicalTrials.gov ↗ ← All trials in the USA