AIR Support: Artificially Intelligent Robot (AIR) Support for Pediatric Asthma Education

University of Miami98 enrolled

Overview

The purpose of this prevention study is to evaluate the design and usability of a newly developed asthma education protocol with the Human Support Robot (HSR) for children with asthma.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Enrollment

Conditions

Asthma in Children Artificial Intelligence

Interventions

Standard Asthma EducationBEHAVIORAL

Participants will receive the usual asthma education provided by their healthcare provider during the clinic visit, including asthma action plan and metered dose inhaler and spacer teaching..

Artificially Intelligent Robot (AIR) Support InterventionBEHAVIORAL

Participants will receive a single 15-minute robotic asthma education session delivered by the Artificially Intelligent Robot/Human Support Robot (AIR/HSR).

Eligibility

Sex: ALLMin age: 3 Years

Medical Language ↔ Plain English

Inclusion (Eligibility) Criteria for Caregivers or Parents: * The participant must be at least 18 years old. * The participant must be willing and able to participate. * The participant can read English or Spanish and is able to fill out survey instruments by themselves or with assistance. * The participant cares for a child with asthma. Exclusion (Eligibility) Criteria for Caregivers or Parents: * The participant is younger than 18 years old. * The participant is unwilling to participate in the study. * The participant is unable to complete survey instruments. * The participant does not care for a child with asthma. Inclusion (Eligibility) Criteria for Children: * The participant must be at least 3 years old - 17 years old with asthma. * The participant must assent to participation. * The participant's guardian must have consented. Exclusion (Eligibility) Criteria for Children: * The participant is younger than 3 years old. * The participant does not have asthma. * The participant is unwilling to participate in the study. * The participant's guardian did not consent. Inclusion (Eligibility) Criteria for Healthcare Providers: * The participant must be at least 18 years old. * The participant must be willing and able to participate. * The participant can read English and is able to fill out survey instruments by themselves. * The participant must view a robotic education session.

Locations (1)

Batchelor Children's Research Institute

Miami, Florida, United States

Outcomes

Primary Outcomes

Feasibility of the Human Support Robot: Enrollment Rate

Feasibility will be assessed by measuring the enrollment rate for the study involving the Human Support Robot. Enrollment rate will be calculated as the number of participants enrolled divided by the number of eligible participants approached, expressed as a percentage. Higher percentages indicate greater feasibility of implementation.

Time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.

Feasibility of the Human Support Robot: Completion Rate

Feasibility will be evaluated by measuring the completion rate for the study procedures involving the Human Support Robot. Completion rate will be calculated as the number of enrolled participants who complete all required study procedures - including the education session, survey, inhaler-use demonstration, and interview - divided by the total number of participants enrolled, expressed as a percentage. Higher percentages indicate greater feasibility of implementation.

Time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.

Feasibility of the Human Support Robot: Session Length

Feasibility will be measured by recording the duration in minutes of the robot education session. More consistent and shorter session durations indicate better feasibility for clinic workflow and integration of the Human Support Robot.

Time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.

Feasibility of the Human Support Robot: Number of Technical Issues

Feasibility will be assessed by recording the number and type of technical issues occurring during the robot-supported education session, including hardware malfunctions, software errors, or disruptions requiring staff assistance. Fewer technical issues indicate greater feasibility of implementing the Human Support Robot in a clinic setting.

Time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.

Data from ClinicalTrials.gov

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Secondary Outcomes

Child Engagement (PROMIS)

Child engagement will be evaluated using a slightly adapted Patient-Reported Outcomes Measurement Information System (PROMIS) Early Childhood Parent Engagement measure. This questionnaire includes items assessing the child's attention, interest, and participation during activities. Each item is rated on a 5-point Likert scale ranging from 1 ("never") to 5 ("always"). Item responses are summed and converted to a standardized T-score (mean = 50, standard deviation = 10). Higher T-scores indicate greater engagement.

Time frame: Day 1

Child inhaler technique (Coaching Tool)

Child knowledge will be assessed using the Inhaler Technique Coaching Tool, a structured checklist evaluating each step of proper inhaler use. The research assistant will score each step as correct (1) or missed or done improperly (0). Scores will be summed to produce a total score ranging from 0 - 6, with higher scores indicating more accurate inhaler technique and greater knowledge of inhaler use.

Time frame: Day 1