Ignite Creation Date:
2024-05-19 @ 5:35 PM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06417996
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-16
First Post:
2024-02-21
Brief Title:
Biobeat Digital Home Monitoring Feasibility
Sponsor:
Lawson Health Research Institute
Organization:
Lawson Health Research Institute
Study Overview
Official Title:
Postoperative Digital Care Home Monitoring
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-05
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
Detailed 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 Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None