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

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University of Miami

Status

Begins enrollment this month

Conditions

Artificial Intelligence
Asthma in Children

Treatments

Behavioral: Standard Asthma Education
Behavioral: Artificially Intelligent Robot (AIR) Support Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT07387718
20251352

Details and patient eligibility

About

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.

Enrollment

120 estimated patients

Sex

All

Ages

3+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

Standard Asthma Education (Control)
Active Comparator group
Description:
Participants in this arm will receive one standard asthma education session during a single clinic visit lasting approximately 5 minutes.
Treatment:
Behavioral: Standard Asthma Education
Standard Education Plus Artificially Intelligent Robot (AIR) Support Intervention (Experimental)
Experimental group
Description:
Participants in this arm will receive standard asthma education plus one artificially intelligent robot supported education session during a single clinic visit lasting approximately 15 minutes.
Treatment:
Behavioral: Artificially Intelligent Robot (AIR) Support Intervention
Behavioral: Standard Asthma Education

Trial contacts and locations

1

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Central trial contact

Ubbo Visser, PhD; Cynthia L Foronda, PhD

Data sourced from clinicaltrials.gov

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