Completed

A Mobile Health Solution to Improve Between-Session Skills Practice in Youth Mental Health Treatment

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What is being tested

Cognitive Behavioral Therapy (CBT)

+ CBT+App

Behavioral
Who is being recruted

Trauma and Stressor Related Disorders+7

+ Psychological Well-Being

+ Anxiety Disorders

From 7 to 17 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: June 2021
See protocol details

Summary

Principal SponsorUniversity of South Florida
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: June 10, 2021

Actual date on which the first participant was enrolled.

The purpose of this study is to preliminarily evaluate a web-based app to improve provider implementation and patient engagement in homework (i.e., between-session practice of skills learned during therapy) during child mental health treatment by conducting a small-scale feasibility trial in community practice settings comparing Cognitive Behavioral Therapy (CBT) to CBT enhanced with the app.

Official TitleA Mobile Health Solution to Improve Between-Session Skills Practice in Youth Mental Health Treatment
NCT04931199
Principal SponsorUniversity of South Florida
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

86 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 7 to 17 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Trauma and Stressor Related DisordersPsychological Well-BeingAnxiety DisordersBehaviorMental DisordersBehavioral SymptomsDepressionPersonal SatisfactionStress Disorders, Post-TraumaticStress Disorders, Traumatic

Criteria

Inclusion Criteria: Providers: * English-speaking * Mental health providers who have obtained at least a master's degree in social work, counseling, clinical psychology, or related field * Carry active child mental health treatment caseloads * Have a laptop, tablet, or smartphone with internet access Youth: * English-speaking * Youth Ages 7-17 years * Clinically elevated anxiety and depression as indicated by a T-score ≥ 65 on the Revised Children's Anxiety and Depression Scale-25 Child Version (RCADS-25-Y) and/or Revised Children's Anxiety and Depression Scale-25 Parent Version (RCADS-25-P) or total score ≥ 15 on the Child and Adolescent Trauma Screen - Youth Report (CATS-Y) and/or Child and Adolescent Trauma Screen - Caregiver Report (CATS-P) * Have a laptop, tablet, or smartphone with internet access Caregivers: * English-speaking * Adult (≥18 years old) * Caregivers of a youth who meets eligibility criteria * Have internet and smartphone access. Exclusion Criteria: Youth with self- or caregiver-reported: * Active psychotic symptoms (e.g., hallucinations, delusions) * Significant cognitive disability, developmental delays, or pervasive developmental disorder.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator

Group II

Experimental

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

University of South Florida

Tampa, United StatesOpen University of South Florida in Google Maps
CompletedOne Study Center