Pilot testing a device for continuous monitoring of vital signs in older adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the feasibility and accessibility of the Continuous Connected Patient Care (CCPC) platform, which includes various monitoring technologies, in both hospital and home settings for older adults. The study will involve inpatients from the Acute Care for Elderly Unit and will assess how well the device can be integrated into their care. The goal is to determine if this technology can effectively monitor vital signs continuously and improve patient care.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Inpatients on the Acute care of the Elderly ward.

Exclusion Criteria:

* 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

Where it's running

• St. Paul'sHospital
  Vancouver, British Columbia, Canada Recruiting

Study contacts

• Study coordinator: Elise Huisman
• Email: elise.huisman@medtronic.com
• Phone: +1 236-308-4876

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.