Development of an AI Assessment System for Pediatric Respiratory Distress : A Prospective Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-12
SponsorSamsung Medical Center

About this trial

This is a multicenter, prospective observational study designed to collect clinical data for the development of a vision-language model-based artificial intelligence system for automated assessment of pediatric respiratory patterns.

The study enrolls pediatric patients aged 0 to 12 years who present to the pediatric emergency departments of participating institutions. Clinical and visual respiratory data are collected along with baseline clinical characteristics, including sex, age, body weight, height, presenting symptoms recorded at emergency department arrival, initial vital signs (body temperature, pulse rate, respiratory rate, blood pressure, and oxygen saturation), severity at presentation assessed by the Korean Triage and Acuity Scale (KTAS), emergency department management and outcomes such as hospital admission or discharge, and other relevant clinical information.

These data are used for cohort characterization and for the development and evaluation of an AI-based system that aims to automatically analyze pediatric respiratory patterns and support objective respiratory assessment in pediatric emergency care.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pediatric patients aged 0 to 12 years who present to participating pediatric emergency departments.

Patients for whom clinical data, including basic demographic characteristics (e.g., age, body weight), severity at presentation (e.g., KTAS level), vital signs, emergency department management and outcomes, as well as visual respiratory data, are available during emergency care.

Disqualifiers

Patients outside the specified age range.

Patients with insufficient or poor-quality clinical or visual respiratory data.

Patients whose data cannot be used due to withdrawal of consent or regulatory restrictions.

Trial population

The study population consists of pediatric patients aged 0 to 12 years who visit the pediatric emergency departments of participating institutions. Clinical data, including basic demographic characteristics (e.g., sex, age, body weight, height), severity at presentation (e.g., KTAS level), vital signs, and emergency department management and outcomes (e.g., admission or discharge), as well as visual respiratory data, are collected during emergency care and used for the development and evaluation of a vision-language model-based system for automated assessment of pediatric respiratory patterns.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

2,200 Participants
are grouped into 1 trial group
Group A: Pediatric Emergency Department Patients

Trial outcomes

Primary outcomes

1

Accuracy of automated respiratory pattern assessment

Performance of a vision-language model-based system in assessing pediatric respiratory patterns using clinical and visual respiratory data collected in pediatric emergency departments.

Time frame
From study start through study completion (up to December 2027)

Secondary outcomes

Other outcomes

Sponsors and contacts

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