Digital Therapeutics for Behavior Problems

Sponsor
University of Pittsburgh (Other)
Overall Status
Recruiting
CT.gov ID
NCT05647772
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
324
1
3
51.9
6.2

Study Details

Study Description

Brief Summary

In this project, the investigators aim to test the effectiveness of a mobile health (mHealth) system as a standalone versus coach-assisted intervention with the goal of achieving reach and scalability. Parents of children (ages 5-8) with disruptive behaviors (N = 324 subjects) will be randomly assigned to Group 1 (standalone app), Group 2 (coach-assisted app), or Group 3 (control app).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: UseIt! App
  • Behavioral: Coach
  • Behavioral: SmilingMind App
N/A

Detailed Description

In this project, the investigators aim to test the effectiveness of a mobile health (mHealth) system as a standalone versus coach-assisted intervention with the goal of achieving reach and scalability. Aim 1 is to evaluate the effectiveness of the UseIt! mHealth system as both a standalone and coach-assisted intervention compared to a control app condition. Aim 2 is to assess target (parent management training/cognitive behavioral therapy skill acquisition and use) engagement and validation. Aim 3 is to evaluate the effectiveness of the components of the UseIt! mHealth system. The investigators plan to recruit an anticipated total of 324 families for the study. Families will be randomly assigned to Group 1 (standalone app), Group 2 (coach-assisted), or Group 3 (control app condition). Parents will use the app for four months before the administration of the post-treatment assessment. Parents will be trained to use the UseIt! mHealth system over the phone. The coach for the Group 2 condition will be a bachelor's level paraprofessional with a degree in psychology or an allied discipline (e.g., social work) who will provide support to parents. The system is very user friendly and families can be trained in approximately 30 minutes. Assessments will take place at Baseline, Post (4 months from baseline), and 6-month follow-up. All assessments will be conducted online (Qualtrics survey links sent via email by research staff) and take approximately 1 hour to complete.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
324 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study is a randomized control trial. The investigators will use stratified randomization to ensure that the groups are equivalent on key clinical features. Randomization will take place after completion of the initial baseline assessment. Parents of children (ages 5-8) with disruptive behaviors (N = 324 subjects) will be randomly assigned to Group 1 (standalone app; n = 108), Group 2 (coach-assisted app; n = 108), or Group 3 (control app; n = 108).This study is a randomized control trial. The investigators will use stratified randomization to ensure that the groups are equivalent on key clinical features. Randomization will take place after completion of the initial baseline assessment. Parents of children (ages 5-8) with disruptive behaviors (N = 324 subjects) will be randomly assigned to Group 1 (standalone app; n = 108), Group 2 (coach-assisted app; n = 108), or Group 3 (control app; n = 108).
Masking:
Single (Investigator)
Primary Purpose:
Health Services Research
Official Title:
Reach and Scalability of Digital Therapeutics for Childhood Behavior Problems
Actual Study Start Date :
Dec 3, 2022
Anticipated Primary Completion Date :
Oct 1, 2026
Anticipated Study Completion Date :
Apr 1, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1: Standalone App

Standalone parenting app called UseIt!

Behavioral: UseIt! App
The UseIt! app is a parenting app with evidence-based parent management content. The app runs on both Android and iOS devices. It includes a digital library of parent management skills, a trouble-shooting guide, a behavior diary, a point counter, and a skills-alarm.

Experimental: Group 2: App plus Coach

Standalone parenting app called UseIt! plus a coach.

Behavioral: UseIt! App
The UseIt! app is a parenting app with evidence-based parent management content. The app runs on both Android and iOS devices. It includes a digital library of parent management skills, a trouble-shooting guide, a behavior diary, a point counter, and a skills-alarm.

Behavioral: Coach
The coach is be a bachelor's level paraprofessional with a degree in psychology or an allied discipline (e.g., social work) who provides support to parents. The coach will provide motivation and accountability but will not provide therapeutic/clinical support. The primary goal of the coach is to increase participant engagement with the UseIt! mHealth system.

Active Comparator: Group 3: Control App

Control condition: mindfulness app called SmilingMind.

Behavioral: SmilingMind App
The control app is a mindfulness app called SmilingMind. It is available for both Android and iOS devices.

Outcome Measures

Primary Outcome Measures

  1. Knowledge of Effective Parenting Test (KEPT) [Post assessment (4 months after baseline).]

    Average scores from the Knowledge of Effective Parenting Test (KEPT). This is a 21-item scale, with higher scores indicating better outcomes.

  2. Knowledge of Effective Parenting Test (KEPT) [6-month follow-up (10 months after baseline).]

    Average scores from the Knowledge of Effective Parenting Test (KEPT). This is a 21-item scale, with higher scores indicating better outcomes.

Secondary Outcome Measures

  1. Parenting Skill Use Diary (PSUD) [Post assessment (4 months after baseline).]

    Average scores from the Parenting Skill Use Diary (PSUD). This is a proportion score (range 0 to 1), with higher scores indicating better outcomes.

  2. Parenting Skill Use Diary (PSUD) [6-month follow-up (10 months after baseline).]

    Average scores from the Parenting Skill Use Diary (PSUD). This is a proportion score (range 0 to 1), with higher scores indicating better outcomes.

  3. Oppositional Defiant Disorder Subscale of the Vanderbilt Assessment [Post assessment (4 months after baseline).]

    Average scores from the Oppositional Defiant Disorder Subscale of the Vanderbilt Assessment. Scores range from 0 to 24, with higher scores indicating worse outcomes.

  4. Oppositional Defiant Disorder Subscale of the Vanderbilt Assessment [6-month follow-up (10 months after baseline).]

    Average scores from the Oppositional Defiant Disorder Subscale of the Vanderbilt Assessment. Scores range from 0 to 24, with higher scores indicating worse outcomes.

  5. Conduct Disorder Subscale of the Vanderbilt Assessment [Post assessment (4 months after baseline).]

    Average scores from the Conduct Disorder Subscale of the Vanderbilt Assessment. Scores range from 0 to 42, with higher scores indicating worse outcomes.

  6. Conduct Disorder Subscale of the Vanderbilt Assessment [6-month follow-up (10 months after baseline).]

    Average scores from the Conduct Disorder Subscale of the Vanderbilt Assessment. Scores range from 0 to 42, with higher scores indicating worse outcomes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
5 Years to 8 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Males or females between the ages of 5-8 years

  • Above the 90th percentile for Oppositional Defiant Disorder (ODD) and/or conduct disorders (CD) on the Vanderbilt Assessment Scale

  • Residence with at least one parent/guardian at least 80% of the time

  • Parent/legal guardian consent for participation

  • Parent/guardian must have a smartphone device with daily internet access

Exclusion Criteria:
  • A known preexisting behavioral or mental health diagnosis requiring alternative treatment (bipolar disorder, major depression, pervasive developmental disorder)

  • Currently in treatment for childhood disruptive behavior

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bellefield Towers Pittsburgh Pennsylvania United States 15213

Sponsors and Collaborators

  • University of Pittsburgh
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Investigators

  • Principal Investigator: Oliver Lindhiem, PhD, University of Pittsburgh, Department of Psychiatry

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Oliver Lindhiem, Associate Professor, University of Pittsburgh
ClinicalTrials.gov Identifier:
NCT05647772
Other Study ID Numbers:
  • STUDY22030138
  • R01HD106930
First Posted:
Dec 12, 2022
Last Update Posted:
Dec 12, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Oliver Lindhiem, Associate Professor, University of Pittsburgh
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 12, 2022