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Clinical Trials/NCT06443918
NCT06443918
Completed
Not Applicable

A Just-in-Time Adaptive Intervention for Child and Family Mental Health

Colliga Apps Corp.2 sites in 1 country347 target enrollmentMay 20, 2024

Overview

Phase
Not Applicable
Intervention
A Just-in-Time Adaptive Intervention for Child and Family Mental Health
Conditions
Mental Health and Well-being
Sponsor
Colliga Apps Corp.
Enrollment
347
Locations
2
Primary Endpoint
Change in child internalizing symptoms, measured by the Child Behavior Checklist (CBCL) Internalizing Problems scale
Status
Completed
Last Updated
last month

Overview

Brief Summary

The goal of this clinical trial is to test an app-based just-in-time-adaptive intervention (JITAI). The intervention aims to improve child and family mental health. A JITAI provides in-the-moment feedback to coach families. The questions it tests are if the app will improve mental health and family functioning. Participants will download an app on their phone and complete JITAI sessions. Researchers will compare intervention and control groups to see if the app improves mental health.

Detailed Description

The following study tests the efficacy of an app-based program designed to improve child and family mental health and well-being. The intervention will include family-based activities for improving child and family mental health and functioning delivered as psychoeducation and activities through the smartphone app, as well as a just-in-time adaptive intervention (JITAI) component where AI analysis for family interactions will be used to provide real-time, dynamic feedback to families. Participants will be informed during consent that they will have a 50-50 chance of receiving the intervention. The study will assess caregiver and child functioning in a variety of domains, such as mental health symptoms, attachment style, and family conflict through a series of baseline and follow-up questionnaires. Caregivers may use their own smartphones, or they will be lent smartphones for the study. Caregivers and children will also be lent Fitbits/Apple Watches. The intervention will last 8 weeks. Data will include daily surveys, daily audio recordings, 15-minute surveys every 2 weeks about their experiences using the app, bi-weekly check-ins, psychoeducational modules, homework activities, JITAI sessions, and passively sensed data. The intervention will be administered through the smartphone app and will include daily 5-15-minute psychoeducation modules and practice sessions and daily JITAI sessions.

Registry
clinicaltrials.gov
Start Date
May 20, 2024
End Date
January 14, 2026
Last Updated
last month
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Colliga Apps Corp.
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • A family income less than or equal to the 33rd percentile for their county of residence OR
  • At least one participating family member identifies as belonging to an ethnic/racial minoritized group AND
  • Child mental health symptoms at or above the 70th percentile based on any subscale of the Strengths and Difficulties Questionnaire AND
  • Participants speak English and/or Spanish AND
  • Have a child 6-9 years old at the time of enrollment AND
  • Families must be located in Texas or Florida

Exclusion Criteria

  • Active suicidal ideation OR
  • Active homicidal ideation OR
  • Current child abuse OR
  • Current violence in the home
  • Families meeting these exclusion criteria will undergo a clinical risk assessment and be referred for alternative treatment services.

Arms & Interventions

Intervention

The intervention aims to improve child and family mental health and functioning through psychoeducation and family-based activities delivered via a smartphone app. This intervention also includes a just-in-time adaptive intervention (JITAI) for coaching family interactions in real-time. Caregivers will wear smartwatches and carry smartphones for 8 weeks. Children will wear smartwatches. A variety of types of data will be collected from the phones and watches, such as heart rate, activity levels, and sleep. We will also collect daily surveys, daily audio recordings, a 15-minute survey every 2 weeks about their experiences using the app, and check-in calls every 2 weeks.

Intervention: A Just-in-Time Adaptive Intervention for Child and Family Mental Health

Control group

Caregivers will wear smartwatches and carry smartphones for 8 weeks. Children will wear smartwatches. Participants will complete placebo psychoeducational modules matched in length and reading level to the intervention content. A variety of types of data will be collected from the phones and watches, such as heart rate, activity levels, and sleep. We will also collect daily surveys, daily audio recordings, a 15-minute survey every 2 weeks about their experiences using the app, and check-in calls every 2 weeks.

Outcomes

Primary Outcomes

Change in child internalizing symptoms, measured by the Child Behavior Checklist (CBCL) Internalizing Problems scale

Time Frame: 8 weeks

Assesses caregiver-reported child internalizing symptoms (e.g., anxiety, depression, withdrawal) using the Child Behavior Checklist (CBCL) Internalizing Problems scale, evaluated as change from baseline to post-intervention follow-up to determine intervention effects on child emotional functioning.

Secondary Outcomes

  • Child externalizing symptoms, measured by the Child Behavior Checklist (CBCL) Externalizing Problems scale(8 weeks)
  • Caregiver mental health symptoms, measured by the 27-Plus (SCL-27-Plus) total score(8 weeks)
  • Child attachment(8 weeks)
  • Caregiver attachment(8 weeks)
  • Parent-child aggression(8 weeks)
  • Inter-parental aggression(8 weeks)

Study Sites (2)

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