Health TrialsbyHealthPanel

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

ConditionsSurgical Procedure, UnspecifiedIntensive Care Units (ICUs)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age19+
SponsorMedtronic - MITG

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial population

Patients that have undergone a non-cardiac surgery requiring an inpatient hospital stay and peri-op patients who are in the Surgical High Acuity Unit (SHAU) at SPH.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Collect patient and clinicians' feedback about the CCPC Platform

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.

Time frame
From enrollment to the end of follow up at 10 days
2

Confirm the technical goals of the CCPC platform are met.

This will be completed by ensuring clinical workflow is met when using the monitoring platform.

Time frame
From enrollment to the end of follow up at 10 days
3

Collect patient and clinicians' feedback about the CCPC Platform

This will be completed via an assessment of the Usability questionnaires.

Time frame
From enrollment to the end of follow up at 10 days
4

Collect patient and clinicians' feedback about the CCPC Platform

This will be completed by an evaluation of potential harm, adverse events and safety issues.

Time frame
From enrollment to the end of follow up at 10 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Medtronic - MITG

Lead sponsor

Excelar

Collaborator

Cloud DX Inc.

Collaborator

Bridge Health Solutions

Collaborator

Providence Healthcare

Collaborator

Source ClinicalTrials.gov
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