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Recruiting

NCT Number: NCT06638073

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

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.

Recruiting

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Key information

Conditions

Surgical Procedure, Unspecified Intensive Care Units (ICUs)

Age range

19 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Saint Pauls Hospital

Vancouver, British Columbia, V6Z 1Y6, Canada

Location status: Recruiting

Location contact

Ronald Ree, MD

CONTACT

[email protected]

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. Collect patient and clinicians' feedback about the CCPC Platform

    Time frame: 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.

  2. Confirm the technical goals of the CCPC platform are met.

    Time frame: 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.

  3. Collect patient and clinicians' feedback about the CCPC Platform

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

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

  4. Collect patient and clinicians' feedback about the CCPC Platform

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

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

  5. Confirm the technical goals of the CCPC platform are met.

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

    This will be completed via an assessment of the data flow: does the correct patient vitals information reach the clinicians at the right time?

  6. Confirm the technical goals of the CCPC platform are met.

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

    This will be completed by determining if the CCPC platform provided a holistic view of each patient with vitals, medication, and other collected data.

Study contacts

Contact information is provided by the study sponsor or research team.

Elise Huisman

CONTACT

[email protected]

+1 236-308-4876

Sponsors and collaborators

Lead sponsor

Medtronic - MITG

Industry

Collaborators

  • Bridge Health Solutions
  • Cloud DX Inc.
  • Excelar
  • Providence Healthcare

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Oct 15, 2024
Registry last updated
Mar 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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