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RECRUITING
NCT06565390
NA

Remote Oximeter Monitoring Post-discharge to Reduce Emergency Room Visits and Rehospitalization

Sponsor: University of Alabama at Birmingham

View on ClinicalTrials.gov

Summary

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.

Official title: Remote Oximeter Monitoring Post-discharge to Reduce Emergency Room Visits and Rehospitalization (ROMPER): A Randomized Clinical Trial

Key Details

Gender

All

Age Range

22 Weeks - 6 Months

Study Type

INTERVENTIONAL

Enrollment

700

Start Date

2025-09-11

Completion Date

2030-12-31

Last Updated

2025-09-30

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Babies in the Owlet monitor group

The Owlet group will be given an Owlet OSS 3.0 monitor to wear when sleeping. The Owlet alarms if the baby has a very low heart rate or very low oxygen levels. In addition, caregivers in the Owlet group with a smart phone and Wi-Fi access will be able to use an application to monitor the baby's vital signs and sleep state.

Locations (1)

University of Alabama at Birmingham

Birmingham, Alabama, United States