Biobeat Digital Home Monitoring Feasibility

Status Not yet recruiting

Clinical Trial Summary

To assess the feasibility of evaluating postoperative home monitoring with Biobeat digital monitoring. The investigators hypothesize that the Biobeat digital home monitoring platform will lead to a decrease in unplanned visits to the ED (Emergency Department). In addition, patients' quality of life is postulated to be improved compared to patients receiving the current standard of care without home monitoring.

Clinical Trial Description

This trial will be a single centre, parallel arm, randomized controlled feasibility trial. The investigators will evaluate postoperative home monitoring with the Biobeat digital monitoring and two-way communication through the digital portal for 4 weeks post-operatively to the standard of care (no digital monitoring) in thoracic surgery patients undergoing elective thoracic surgical procedures. The investigators will assess whether conducting a larger randomized trial of digital home monitoring vs. standard of care is feasible in terms of recruitment, data collection and logistics. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06417996
Study type	Interventional
Source	Lawson Health Research Institute
Contact	Deb Lewis
Phone	5196858500
Email	deb.lewis@lhsc.on.ca
Status	Not yet recruiting
Phase	N/A
Start date	June 30, 2024
Completion date	May 31, 2025

View Details

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