Remote Oximeter Monitoring Post-discharge to Reduce Emergency Room Visits and Rehospitalization
Recruiting
N/A
Interventional Study
Emergencies
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 22 Weeks – 6 Months
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 700 (estimated)
- Sponsor
- University of Alabama at Birmingham · Other
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About This Trial
This randomized clinical trial will determine the efficacy of remote patient monitoring using an Owlet OSS 3.0 pulse oximeter for the reduction of emergency room visits and high-acuity rehospitalizations among high-risk infants after NICU discharge.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Infants being discharged from the NICU
* Off all respiratory support (oxygen, CPAP, ventilator) before discharge home
* Gestational age ≥ 22 0/7 weeks' gestation at birth
* Parents/legal guardians have provided consent for enrollment
Exclusion Criteria:
* a major malformatio…
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