Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Older Adults Department PHC

NCT06638060 | Recruiting

• 1 other identifier: H24-00744
• Study Type: observational
• Target: 15
• Locations: 1 country
• Sites: 1

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 - 1) hospital (Acute Care for Elderly Unit) and 2) at-home .

Conditions

Aging

Outcome Measures

Primary Outcomes (6)

• 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.

  From enrollment to the end of follow up at 10 days

• Collect patient and clinicians' feedback about the CCPC Platform

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

  From enrollment to the end of follow up at 10 days

• Collect patient and clinicians' feedback about the CCPC Platform

  This will be completed by an evaluation for potential harm, e.g. anxiety questionnaire and any patient-reported adverse events.

  From enrollment to the end of follow up at 10 days

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

  This will be completed by ensuring clinician workflow is met, via feedback sessions (e.g. conversations, questionnaires).

  From enrollment to the end of follow up at 10 days

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

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

  From enrollment to the end of follow up at 10 days

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

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

  From enrollment to the end of follow up at 10 days

Eligibility Criteria

• Age: 65 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

The Acute Care for Elderly Unit at SPH for 40 inpatients over the age of 65.

You may qualify if:

• Inpatients on the Acute care of the Elderly ward.

You may not qualify if:

• Lack of capacity to consent to the study including moderate-severe dementia or delirium
• 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
• Patient with known allergic reactions to any part material of the device
• People under 40kg

Sponsors & Collaborators

• Medtronic - MITG: lead
• Excelar: collaborator
• Cloud DX Inc.: collaborator
• Bridge Health Solutions: collaborator
• Providence Healthcare: collaborator

Study Sites (1)

St. Paul'sHospital

Vancouver, British Columbia, V6Z 1Y6, Canada

RECRUITING

Central Study Contacts

Elise Huisman

CONTACT

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

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 16, 2024
• First Posted: October 15, 2024
• Study Start: March 13, 2025
• Primary Completion (Estimated): June 21, 2026
• Study Completion (Estimated): June 21, 2026
• Last Updated: March 12, 2026

Record last verified: 2025-05

Data Sharing

• IPD Sharing: Will not share

Locations

CA (1)