Continuous Connected Patient Care (CCPC), a Pilot Testing a Novel Device for Continuous Vitals Monitoring - Department of Anesthesia at PHC
This study is looking at a new system called "Continuous Connected Patient Care" (CCPC) for people having non-heart surgery. It wants to see how well it works and how easy it is to use. The system includes a special device for monitoring vital signs (like heart rate and breathing), health software, and a home kit. Researchers will test this in two places: while patients are in the hospital's high-acuity unit and after they go home. The main goal is to check if this new way of monitoring is practical and accessible for patients in British Columbia, Canada, to help improve their care after surgery.
At a glance
What is this study about?
Imagine you've had surgery, and even after you leave the hospital, doctors could still keep a close eye on your health from afar. This study, called "Continuous Connected Patient Care" (CCPC), is exploring just that. It's testing a new system designed to continuously monitor important health signals, often called 'vital signs,' both when you're in the hospital and once you're back home.
The main idea is to see if this new system is easy to use and genuinely helpful for patients who've had surgery that isn't related to their heart. The system combines different pieces of technology, including a monitoring device, health software, and a kit you can use at home. By checking how well it works in different settings, the researchers hope to make patient care after surgery more connected and reassuring.
This is a pilot study, which means it’s an early test to see if the idea is sound before rolling it out more widely. If it proves to be effective and easy for patients to use, it could potentially change how we look after people after surgery, giving doctors more information and patients more peace of mind.
Key takeaways
- Tests a new system for monitoring health after surgery.
- Aims to make care more connected from hospital to home.
- Uses a special device and software to track vital signs.
- Focuses on non-heart surgery patients in British Columbia.
- A 'pilot' study, meaning it's an early test of the system.
Who may be eligible?
To be part of this study, you need to be 19 years old or older and have recently had a non-heart surgery at St. Paul's Hospital that required you to stay overnight. You'd also need to be in the special Surgical High Acuity Unit or being looked after by the Anesthesia team after your surgery.
It's also important that you live in British Columbia, Canada, and your home area has good mobile phone coverage from Bell. This is because the system relies on mobile network to send information.
There are also some reasons why you might not be able to join. For example, if you don't want to, or if you're unable to understand and agree to take part. This also includes if you've recently had strong pain relief or a general anaesthetic. You also need to be able to use the monitoring device at home, or have someone who can help you with it, and be able to fill out questionnaires, either on a device, on paper, or over the phone. If you're planning to go to a nursing home or rehabilitation centre after surgery, or if you're allergic to any parts of the study devices, you wouldn't be able to join.
Could this study suit you?
Answer these quick questions to see if you may be eligible. This is a guide only — the research team makes the final call.
- Are you 19 years old or older?
- Did you have non-heart surgery at St. Paul's Hospital recently, staying overnight?
- Do you live in British Columbia and have Bell mobile coverage?
- Can you or a helper use a monitoring device and fill out questionnaires?
- Are you able to agree to take part in the study?
What does participation involve?
If you decide to take part in this study, you would be using a special monitoring device that keeps track of your vital signs, initially in the hospital and then at home. You'll also need to be able to complete questionnaires, which can be done on a mobile phone, tablet, computer, or even on paper or over the phone. The study doesn't involve visits to a special clinic or taking any new medications. The main focus is on using the monitoring device and sharing your health information. The total duration of your participation would involve the time you're in the hospital after your surgery and then a period at home where you continue to use the monitoring kit and complete the questionnaires.
Potential risks and benefits
Locations (1)
- Saint Pauls HospitalVerified postcodeVancouver, Canada· Recruiting
Common questions
What kind of surgery can I have to join this study?
You need to have had a non-heart surgery that required you to stay overnight in the hospital.
Will I have to travel for this study?
No, you won't need to make special trips. The monitoring happens in the hospital and at your home.
What if I live alone and can't put on the device myself at home?
You can still participate if you have a caregiver who can help you put on the monitoring device.
Do I need to have a smartphone to be part of the study?
You need access to a mobile phone or internet-connected device, or even a landline, for follow-ups and to complete questionnaires.
What does 'non-cardiac surgery' mean?
This simply means any surgery that is not on your heart.
How to find out more
Elise Huisman
Always speak to your GP or specialist before deciding to take part in a study.
Interested in taking part?
Discussion
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