Actively Recruiting
Postoperative Digital Care Home Monitoring for Thoracic Surgery Patients
Led by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · Updated on 2025-03-06
48
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the feasibility of using the Biobeat digital home monitoring platform to support patients after thoracic surgery. The study compares this new digital monitoring approach with the current standard care, aiming to see if it reduces unplanned emergency department visits and improves patients' quality of life. This trial is designed as a single center, randomized controlled study focusing on elective lung cancer surgery patients. Participants are randomly assigned to one of two groups. The control group receives standard care without home monitoring after hospital discharge. The intervention group is provided with a Biobeat digital monitoring kit, including devices to measure non-invasive blood pressure, pulse oximetry, heart rate, and pain scores. They will use these devices twice daily for two weeks, with continuous ECG monitoring via a two-lead patch to detect irregular heart rhythms. Digital communication with healthcare providers is maintained for four weeks post-surgery. During the study, researchers will track patient data collection, recruitment feasibility, and logistics for a future larger trial. They will monitor emergency department visits and hospital readmission rates within 30 days after discharge. Participants' vital signs and pain levels will be reviewed regularly, supported by digital tools. The study lasts for four weeks of active monitoring, with overall feasibility assessed over one year. This approach aims to improve postoperative care through remote monitoring and better communication.
CONDITIONS
Brief Title
Biobeat Digital Home Monitoring Feasibility
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient willing to provide informed consent
- Wi-fi or cellular connectivity at the patient's home
- Patient undergoing elective lung cancer surgery
- Patient familiar/comfortable with the use of technology such as online banking.
You will not qualify if you...
- Patients who are not comfortable with the use of technology.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 2 weeks
Participants in the digital group receive a home monitoring kit at hospital discharge to track vital signs and pain scores twice daily for two weeks through digital communication. The control group receives standard care without digital monitoring.
1 discharge visit and twice daily remote monitoring for 2 weeks
Duration - 30 days from discharge
Participants are monitored for emergency department visits and readmissions for 30 days after discharge to assess health outcomes.
Approximately 1 to 2 follow-up contacts
Trial Site Locations
Total: 1 location
1
London Health Sciences Centre
London, Ontario, Canada, N6A 5W9
Actively Recruiting
Research Team
D
Deb Lewis
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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