Changes to sensor to test

The overall goal of this study is to understand the feasibility of using a wireless sensor device (instead of a wired device) to collect information used to monitor children with heart conditions at home.

The goal of this study is to examine how well continuous sensor-based monitoring performs at detecting physiologic data in infants with single ventricle physiology at home compared to existing approaches, in manner that is feasible and acceptable to patients' families. Performance features of interest include how the data compares to family measurements, whether it correlates with parents' observable symptoms, and how this approach may be integrated into home life and health system workflows. The investigators will also explore whether the collected data can be used to develop predictive analytics for acute deterioration and/or advanced chronic cardiopulmonary management compared to what is currently being done in remote patient monitoring.

Inclusion Criteria:

• Receiving active remote patient monitoring (RPM) in Lurie's Tele-Interstage Home Monitoring Program.
• Age 0-2 years of age at enrollment.
• In the opinion of the investigator, parent or legally authorized guardian, and participant, the participant and (when relevant) family can follow study procedures.

Exclusion Criteria:

• Is going to discontinue RPM before their enrollment would end (i.e., within 14 days).
• Skin breakdown or severe rash at the site of sensor placement.
• Patient without a parental guardian to consent.
• The patient is in active hospice or similar end-of-life care.
• The patient will be living in a long-term institution or transitional facility.

Children receiving remote patient monitoring in tele-interstage home monitoring program.

Data requests will be reviewed by PI if the occur.