Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Department of Anesthesia at PHC

Medtronic

Status: Enrolling

Conditions: Intensive Care Units (ICUs); Surgical Procedure, Unspecified

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT06638073

H24-00862

Details and patient eligibility

About

To confirm feasibility and accessibility of the CCPC Platform (Oxymotion, Bridge Health Solutions medication adherence software, CloudDX home kit) in two different environments - in hospital and at-home, in patients undergoing non-cardiac surgery.

Enrollment: 50 estimated patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 19 years or older
• Patients that have undergone a non-cardiac surgery at SPH requiring an inpatient hospital stay
• Peri-op patients who are in the Surgical High Acuity Unit (SHAU) and those followed by Anesthesia Perioperative Outreach team on the ward
• Living within British Columbia, Canada and in an area that is covered by Bell cellular network

Exclusion criteria

• Patient refusal
• Lack of capacity to consent to the study (including having received sedative or general anesthetic within the past 24 hours)
• Unable to use (or does not have a caregiver who can help put on) study monitoring device at home
• Unable to complete (or does not have a caregiver who can help complete) study questionnaires by electronic (mobile, tablet, or computer), paper, nor phone
• No access to cell phone nor landline at home to receive follow-ups
• Preoperatively known to be discharged to a nursing home or rehabilitation facility
• Known allergic reactions to any part material of study devices