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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06638073

Enrollment

Registered

2024-10-15

Start date

2025-03-13

Completion date

2026-06-20

Last updated

2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive Care Units (ICUs), Surgical Procedure, Unspecified

Brief summary

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

19 Years to No maximum

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

Design outcomes

Primary

Measure	Time frame	Description
Collect patient and clinicians' feedback about the CCPC Platform	From enrollment to the end of follow up at 10 days	This will be completed via an assessment of the quantitative data on how long and how often patients use this monitoring and what were the reasons that patients took the monitors on and off.
Confirm the technical goals of the CCPC platform are met.	From enrollment to the end of follow up at 10 days	This will be completed by ensuring clinical workflow is met when using the monitoring platform.

Countries

Canada

Contacts

CONTACTElise Huisman

elise.huisman@medtronic.com+1 236-308-4876

Outcome results