About this trial
The investigators hypothesize that a simple 3-point tracking device that uses motion sensors attached to the abdomen and chest of a child will provide information regarding thoracoabdominal asynchrony (TAA), a major component of respiratory distress, and ultimately help guide a clinician to initiate, escalate, de-escalate, or stop respiratory support interventions.
AIMS To determine if the TAA-monitoring device can be used to detect differences in respiratory synchrony in a manner that is clinically applicable. The investigators hope that the device will detect 1) major asynchrony events in a timely manner so as to prompt clinician intervention during future use; and 2) asynchrony events that may be less visible to the naked eye that may be precursors to more severe events.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
patients 28-days to 17-years of age
who have respiratory distress and those who do not have respiratory distress
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Objectively monitoring thoracoabdominal asynchrony
Diagnostic testObjectively monitoring thoracoabdominal asynchrony
Treatment groups
Trial outcomes
Primary outcomes
Objectively determine thoracoabdominal asynchrony
The investigators aim to objectively measure the frequency of asynchrony over time (minutes).
Sponsors and contacts
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