CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 2,558 enrolled
Drug / intervention
Wellness +1 morebehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03901274
NCT03901274N/ACompleted
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Patient Centered Enhancements in School Behavioral Health: A Randomized Trial

University of South Carolina·interventional·Posted Apr 3, 2019·Updated Jun 5, 2025

In Brief

A clinical study evaluating Wellness and Partnership for Mental Health. Completed, enrolled 2,558 participants across 3 sites.

Detailed Summary

This study will evaluate whether the evidence-based Wellness framework paired with an evidence-based Partnership compared to Wellness alone will improve middle school students\' social, emotional/behavioral, and academic functioning.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMental Health
CountriesUnited States
CollaboratorsPatient-Centered Outcomes Research Institute, University of Maryland, Baltimore, Medical University of South Carolina

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedApr 3, 2019
Enrollment StartSep 10, 2019
Primary CompletionDec 31, 2023
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 7.2 years ago

Interventions

Wellnessbehavioral

The Wellness framework packages together evidence-based practices of family engagement, modular evidence-based practice, quality assurance, and implementation support. Depending on their time of enrollment, participants can be involved in this condition for one to three years. They will be asked to complete assessments during their therapy sessions periodically throughout the trial.

Partnershipbehavioral

The two patient-centered enhancements are: enhancing mental health literacy and stigma reduction, and improving family-school-mental health partnerships. Depending on their time of enrollment, participants can be involved in this condition for one to three years. They will be asked to complete assessments during their therapy sessions periodically throughout the trial.