--- title: "AIR Support: Artificially Intelligent Robot (AIR) Support for Pediatric Asthma Education" nct_id: NCT07387718 overall_status: ENROLLING_BY_INVITATION phase: NA sponsor: University of Miami study_type: INTERVENTIONAL primary_condition: Asthma in Children countries: United States canonical_url: "https://parkinsonspathways.com/agent/trials/NCT07387718.md" clinicaltrials_gov: "https://clinicaltrials.gov/study/NCT07387718" ct_last_update_post_date: 2026-03-16 last_seen_at: "2026-05-12T06:53:09.085Z" source: ClinicalTrials.gov (mirrored, no enrichment) --- # AIR Support: Artificially Intelligent Robot (AIR) Support for Pediatric Asthma Education **Official Title:** Artificially Intelligent Robot (AIR) Support for Pediatric Asthma Education **NCT ID:** [NCT07387718](https://clinicaltrials.gov/study/NCT07387718) ## Key Facts - **Status:** ENROLLING_BY_INVITATION - **Phase:** NA - **Study Type:** INTERVENTIONAL - **Target Enrollment:** 120 - **Lead Sponsor:** University of Miami - **Conditions:** Asthma in Children, Artificial Intelligence - **Start Date:** 2026-02-10 - **Completion Date:** 2027-03 - **CT.gov Last Update:** 2026-03-16 ## Brief Summary 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. ## Eligibility - **Minimum age:** 3 Years - **Sex:** ALL - **Healthy Volunteers:** No ``` 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. ``` ## Arms - **Standard Asthma Education (Control)** (ACTIVE_COMPARATOR) — Participants in this arm will receive one standard asthma education session during a single clinic visit lasting approximately 5 minutes. - **Standard Education Plus Artificially Intelligent Robot (AIR) Support Intervention (Experimental)** (EXPERIMENTAL) — 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. ## Interventions - **Standard Asthma Education** (BEHAVIORAL) — 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 Intervention** (BEHAVIORAL) — Participants will receive a single 15-minute robotic asthma education session delivered by the Artificially Intelligent Robot/Human Support Robot (AIR/HSR). ## Primary Outcomes - **Feasibility of the Human Support Robot: Enrollment Rate** _(time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.)_ — 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. - **Feasibility of the Human Support Robot: Completion Rate** _(time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.)_ — 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. - **Feasibility of the Human Support Robot: Session Length** _(time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.)_ — 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. - **Feasibility of the Human Support Robot: Number of Technical Issues** _(time frame: Immediately after robotic session and up to 3 months afterwards via recordings and documentation.)_ — 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. - **Acceptability of the Human Support Robot or Acceptability of the Robot-Supported Education Session** _(time frame: Immediately after the robotic session (same clinic visit) and up to 3 months afterwards via recordings and documentation.)_ — Acceptability of the robot will be evaluated by using the Technology Acceptance Model Questionnaire. The questionnaire includes items assessing perceived usefulness and perceived ease of use, each rated on a 7-point Likert scale ranging from 1 ("strongly disagree") to 7 ("strongly agree"). Scores will be averaged to produce subscale scores ranging from 1 to 7, with higher scores indicating greater acceptability. ## Secondary Outcomes - **Child Engagement (PROMIS)** _(time frame: Day 1)_ - **Child inhaler technique (Coaching Tool)** _(time frame: Day 1)_ ## Locations (1) - Batchelor Children's Research Institute, Miami, Florida, United States ## Recent Field Changes (last 30 days) - `status.overallStatus` — added _(2026-05-12)_ - `status.primaryCompletionDate` — added _(2026-05-12)_ - `status.completionDate` — added _(2026-05-12)_ - `status.lastUpdatePostDate` — added _(2026-05-12)_ - `design.phases` — added _(2026-05-12)_ - `design.enrollmentCount` — added _(2026-05-12)_ - `eligibility.criteria` — added _(2026-05-12)_ - `eligibility.minAge` — added _(2026-05-12)_ - `eligibility.sex` — added _(2026-05-12)_ - `outcomes.primary` — added _(2026-05-12)_ - `outcomes.secondary` — added _(2026-05-12)_ - `armsInterventions.arms` — added _(2026-05-12)_ - `armsInterventions.interventions` — added _(2026-05-12)_ - `sponsor.lead` — added _(2026-05-12)_ - `results.hasResults` — added _(2026-05-12)_ - `locations.batchelor children's research institute|miami|florida|united states` — added _(2026-05-12)_ --- *Canonical: https://parkinsonspathways.com/agent/trials/NCT07387718.md* *Source data (authoritative): https://clinicaltrials.gov/study/NCT07387718* *This page is a raw mirror with no AI summary, no editorial enrichment, and no Parkinson's-specific filtering.*