search
Back to results

Reducing Challenging Behaviors in Children With Autism Through Digital Health

Primary Purpose

Autism Spectrum Disorder

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
KeepCalm app
Sponsored by
University of Pennsylvania
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autism Spectrum Disorder focused on measuring emotion regulation, digital mental health, preschool, elementary school, Autism Spectrum Disorder

Eligibility Criteria

3 Years - 13 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Preschool or elementary school child with autism along with a parent and teacher and/or classroom aide
  • Child must have challenging behaviors including but not limited to aggression, escape behavior, loud noises, non-compliance, property destruction, rigid/inflexible behavior, self-injury, and transition difficulties
  • Adult participants must have access to an iPhone in order to test the app or be willing to use a provided study iPhone

Exclusion Criteria:

  • Child does not exhibit challenging behaviors

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    KeepCalm App

    Waitlist Control

    Arm Description

    The KeepCalm app is designed to help manage stress and prevent challenging behaviors in children with autism. The app uses physiological stress tracking, assessed using heart rate monitoring, to indicate when challenging behaviors are likely to occur. The app then recommends strategies to help prevent the onset of challenging behaviors. The app can also be used to track trends in triggers, behaviors, and strategies, and to communicate this information to parents and other members of a child's educational team.

    Individuals assigned to the waitlist control condition will gain access to the KeepCalm app following the study's completion. During the trial, they will not receive any intervention, but will complete baseline and post-intervention measures during the trial.

    Outcomes

    Primary Outcome Measures

    System Usability Scale (SUS)
    The System Usability Scale (SUS) measures perceptions of usability of a given system, in this case, the KeepCalm app. The scale consists of 10 items, each rated on a 5-point Likert Scale from 1 ("Strongly disagree") to 5 ("Strongly agree"). Responses are transformed to get a total range of possible values from 0-100, with higher scores indicating higher perceptions of usability. Typically, a score above 68 is regarded as a good score.
    Acceptability of Intervention Measure (AIM)
    The Acceptability of Intervention Measure (AIM) is used to measure the acceptability of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater acceptability of the intervention.
    Feasibility of Intervention Measure (FIM)
    The Feasibility of Intervention Measure (FIM) is used to measure the feasibility of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater feasibility of the intervention.
    Intervention Appropriateness Measure (IAM)
    The Intervention Appropriateness Measure (IAM) is used to measure the appropriateness of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater appropriateness of the intervention.
    Qualitative interview
    This interview will assess the intervention's usability, appropriateness, feasibility, and acceptability in a qualitative interview format.

    Secondary Outcome Measures

    School Situations Questionnaire (SSQ)
    The School Situations Questionnaire (SSQ) assessing challenging behaviors within the context of school. The scale assesses both the presence and the severity of challenging behaviors by asking the teacher whether or not a given behavior occurs for that child and to rate the severity. The scale yields two summary scores. The first is the number of problems score which is a sum of the number of problems endorsed, ranging from 0-8 with higher scores indicating greater problems endorsed. The second is the mean severity, calculated as the mean severity for the items endorsed, ranging from 1 to 9 with higher numbers indicating more severe problems.
    Institute for Basic Research Modified Overt Aggression Scale (IBR-MOAS)
    The Institute for Basic Research Modified Overt Aggression Scale (IBR-MOAS) measures the frequency and severity of aggressive behavior episodes. The scale is divided into four components: verbal aggression, aggression against property, autoaggression, and physical aggression. There are 4 items in each category, scored from 0-4 (with higher numbers indicating greater severity) and raters can select as many items as are relevant in the category. The items are then summed within each category to create a summed category score, and then each category is multiplied by its specified weight to give a total weighted aggression score, ranging from 0 to 100, with higher scores indicating greater problems with aggression.
    Emotion Dysregulation Inventory (EDI)
    The Emotion Dysregulation Inventory (EDI) measures emotion dysregulation by asking raters to identify how much of a problem certain emotions and behaviors are for the person being rated. The scale consists of 66 items that are rated for how much of a problem the behavior has been in the last 7 days ("not at all", "mild", "moderate", "severe", "very severe"). This ratings are converted into a numerical rating from 0 ("not at all") to 4 ("very severe"), and then summed to create a total score ranging from 0-264, which higher scores indicating greater emotion dysregulation.

    Full Information

    First Posted
    February 4, 2022
    Last Updated
    June 5, 2023
    Sponsor
    University of Pennsylvania
    Collaborators
    Alevio LLC
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT05277194
    Brief Title
    Reducing Challenging Behaviors in Children With Autism Through Digital Health
    Official Title
    Investigating the Impact of an Emotional Stress Alarm App (KeepCalm) on Managing Stress and Preventing Challenging Behaviors in Children With Autism
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    September 2023 (Anticipated)
    Primary Completion Date
    June 2024 (Anticipated)
    Study Completion Date
    June 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Pennsylvania
    Collaborators
    Alevio LLC

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    School-based behavioral approaches to managing challenging behaviors in children with ASD are limited by three key factors: 1) children with ASD often have difficulties communicating their emotions; 2) it is challenging to implement evidence-based, personalized strategies for individual children, and; 3) it is difficult for teachers to track which strategies are successful for individual children. The investigators' personalized mobile-health emotion regulation application (m-health app) will pair heart rate tracking with digital tools to help reduce challenging behavior by supporting stress detection, reminding teachers of specific behavioral strategies and helping teachers to track progress.
    Detailed Description
    The project will develop and pilot test a personalized medicine mobile health emotion regulation application (the m-health KeepCalm app) that incorporates physiological stress measurement to support evidence-based practices for reducing challenging behavior in children with autism spectrum disorder (ASD). As much as 80% of children with ASD exhibit challenging behaviors that can have a devastating impact on personal and family well-being, contribute to teacher burnout and require frequent hospitalization. Evidence-based practices for reducing these behaviors emphasize uncovering triggers, yet parents and teachers often report that challenging behaviors surface without warning. Challenging behaviors caused by emotion dysregulation can be the most difficult to predict, as children with ASD often have difficulty communicating their distress before it results in challenging behavior. Exciting recent advances in digital technology now allow measurement of momentary emotion dysregulation, using physiological indices. The investigators' pilot data from four separate samples demonstrate that increased heart rate predicts onset of challenging behavior in children with ASD. In order to tailor the m-health KeepCalm app to end users and avoid potential barriers to its adoption, in Aim 1, the investigators will evaluate the acceptability, feasibility, and appropriateness of app, and the needs of educational teams in managing stress in children with ASD and challenging behaviors, by conducting interviews with teachers of children with ASD, parents of children with ASD and school administrators, and conducting structured in-class observations with teachers. Through the activities of Aim 2, the researchers will improve the m-health KeepCalm app, building on their initial app prototype, in collaboration with their established research partner, the Translational Informatics Unit, Children's Hospital of Philadelphia, and their established community partner, the School District of Philadelphia. The investigators will do this through 1) exploratory work on the specificity of heart rate increase to challenging behavior, on app clinical decision support timing, and on the association of app false positives and negatives to movement or child factors; 2) monthly advisory board meetings with expert stakeholders for app development guidance, and; 3) rapid-cycle prototyping of the app with 10 educational teams (i.e. 1-2 children with ASD, and their teacher and classroom aide, if they have one). This will allow for iterative improvement based on each user's experience. Through Aim 3, the researchers will test the app for usability, acceptability, feasibility and appropriateness, as well as preliminary effectiveness with 30 educational teams in a randomized waitlist field trial over a 3-month period. Successful completion of these aims will result in a novel m-health app designed to help teachers support emotion regulation, and reduce or prevent challenging behavior in children with ASD, using evidence-based strategies. These activities will lay the foundation for an R01 to evaluate the effectiveness of the m-health KeepCalm app in a full- scale randomized field trial. This proposal aligns with the strategic plan of the Interagency Autism Coordinating Committee, to maximize the potential for technology-based interventions to improve the lives of people with ASD.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Autism Spectrum Disorder
    Keywords
    emotion regulation, digital mental health, preschool, elementary school, Autism Spectrum Disorder

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Sequential Assignment
    Model Description
    Participants will be grouped into teams (child with autism, their teacher, and 1:1/aide) and teams will be randomized to one of the two arms. Teams (n = 10) randomized to the intervention will be given the KeepCalm application to use for 3 months. Teams randomized to the waitlist control condition (n = 10) will be given access to the app following the study's completion.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    20 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    KeepCalm App
    Arm Type
    Experimental
    Arm Description
    The KeepCalm app is designed to help manage stress and prevent challenging behaviors in children with autism. The app uses physiological stress tracking, assessed using heart rate monitoring, to indicate when challenging behaviors are likely to occur. The app then recommends strategies to help prevent the onset of challenging behaviors. The app can also be used to track trends in triggers, behaviors, and strategies, and to communicate this information to parents and other members of a child's educational team.
    Arm Title
    Waitlist Control
    Arm Type
    No Intervention
    Arm Description
    Individuals assigned to the waitlist control condition will gain access to the KeepCalm app following the study's completion. During the trial, they will not receive any intervention, but will complete baseline and post-intervention measures during the trial.
    Intervention Type
    Behavioral
    Intervention Name(s)
    KeepCalm app
    Intervention Description
    The KeepCalm app is designed to help manage stress and prevent challenging behaviors in children with autism.
    Primary Outcome Measure Information:
    Title
    System Usability Scale (SUS)
    Description
    The System Usability Scale (SUS) measures perceptions of usability of a given system, in this case, the KeepCalm app. The scale consists of 10 items, each rated on a 5-point Likert Scale from 1 ("Strongly disagree") to 5 ("Strongly agree"). Responses are transformed to get a total range of possible values from 0-100, with higher scores indicating higher perceptions of usability. Typically, a score above 68 is regarded as a good score.
    Time Frame
    3 months post-baseline
    Title
    Acceptability of Intervention Measure (AIM)
    Description
    The Acceptability of Intervention Measure (AIM) is used to measure the acceptability of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater acceptability of the intervention.
    Time Frame
    3 months post-baseline
    Title
    Feasibility of Intervention Measure (FIM)
    Description
    The Feasibility of Intervention Measure (FIM) is used to measure the feasibility of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater feasibility of the intervention.
    Time Frame
    3 months post-baseline
    Title
    Intervention Appropriateness Measure (IAM)
    Description
    The Intervention Appropriateness Measure (IAM) is used to measure the appropriateness of an intervention. The scale consists of 4 items rated on a 5-point Likert Scale from 1 ("Completely disagree") to 5 ("Completely agree"). The score consists of the sum of the items, ranging from 5 to 20, with higher scores indicating greater appropriateness of the intervention.
    Time Frame
    3 months post-baseline
    Title
    Qualitative interview
    Description
    This interview will assess the intervention's usability, appropriateness, feasibility, and acceptability in a qualitative interview format.
    Time Frame
    3 months post-baseline
    Secondary Outcome Measure Information:
    Title
    School Situations Questionnaire (SSQ)
    Description
    The School Situations Questionnaire (SSQ) assessing challenging behaviors within the context of school. The scale assesses both the presence and the severity of challenging behaviors by asking the teacher whether or not a given behavior occurs for that child and to rate the severity. The scale yields two summary scores. The first is the number of problems score which is a sum of the number of problems endorsed, ranging from 0-8 with higher scores indicating greater problems endorsed. The second is the mean severity, calculated as the mean severity for the items endorsed, ranging from 1 to 9 with higher numbers indicating more severe problems.
    Time Frame
    baseline and 3 months post-baseline
    Title
    Institute for Basic Research Modified Overt Aggression Scale (IBR-MOAS)
    Description
    The Institute for Basic Research Modified Overt Aggression Scale (IBR-MOAS) measures the frequency and severity of aggressive behavior episodes. The scale is divided into four components: verbal aggression, aggression against property, autoaggression, and physical aggression. There are 4 items in each category, scored from 0-4 (with higher numbers indicating greater severity) and raters can select as many items as are relevant in the category. The items are then summed within each category to create a summed category score, and then each category is multiplied by its specified weight to give a total weighted aggression score, ranging from 0 to 100, with higher scores indicating greater problems with aggression.
    Time Frame
    baseline and 3 months post-baseline
    Title
    Emotion Dysregulation Inventory (EDI)
    Description
    The Emotion Dysregulation Inventory (EDI) measures emotion dysregulation by asking raters to identify how much of a problem certain emotions and behaviors are for the person being rated. The scale consists of 66 items that are rated for how much of a problem the behavior has been in the last 7 days ("not at all", "mild", "moderate", "severe", "very severe"). This ratings are converted into a numerical rating from 0 ("not at all") to 4 ("very severe"), and then summed to create a total score ranging from 0-264, which higher scores indicating greater emotion dysregulation.
    Time Frame
    baseline and 3 months post-baseline
    Other Pre-specified Outcome Measures:
    Title
    Artifact removal
    Description
    Number of artifacts detected during the testing period
    Time Frame
    through study participation, an average of 3 months
    Title
    Offline mode activations
    Description
    Proportion of time offline mode is activated over the testing week based on accelerometry data threshold
    Time Frame
    through study participation, an average of 3 months
    Title
    Clinical decision support success
    Description
    Proportion of alarms/emotion regulation strategy app push notifications that result in timely strategy implementation, as measured during the observation session
    Time Frame
    through study participation, an average of 3 months
    Title
    False positives/negatives
    Description
    Proportion of alarms that appear not to be associated with an oncoming challenging behavior (e.g. due to child movement)/challenging behaviors that occurred without an alarm, measured during the observation session
    Time Frame
    through study participation, an average of 3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    3 Years
    Maximum Age & Unit of Time
    13 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Preschool or elementary school child with autism along with a parent and teacher and/or classroom aide Child must have challenging behaviors including but not limited to aggression, escape behavior, loud noises, non-compliance, property destruction, rigid/inflexible behavior, self-injury, and transition difficulties Adult participants must have access to an iPhone in order to test the app or be willing to use a provided study iPhone Exclusion Criteria: Child does not exhibit challenging behaviors
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Heather J Nuske, PhD
    Phone
    2157466041
    Email
    Heather.Nuske@pennmedicine.upenn.edu
    First Name & Middle Initial & Last Name or Official Title & Degree
    David S Mandell, ScD
    Phone
    2155737494
    Email
    David.Mandell@pennmedicine.upenn.edu

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

    Learn more about this trial

    Reducing Challenging Behaviors in Children With Autism Through Digital Health

    We'll reach out to this number within 24 hrs