A randomized intervention study on the effects of telemonitoring in the aftercare of patients after cardiac surgery. A pilot

Completed

• Conditions: bypass surgery; coronary artery bypass grafing; valve surgery; 10007593

• Registration Number: NL-OMON34146
• Lead Sponsor: Medisch Spectrum Twente

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

all patients with CABG, valve surgery and a combination of CABG/valve surgery
Age 55-85 year
Capable to use the equipment

Exclusion Criteria

No comprehension of dutch language
Bad mobility
Patients outside the clinical pathway
Patients transferred to other hospitals

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Quality of life - measured with the SF-36 (Aaronson et al., 1998)</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Number of complications and readmissions within four weeks</p><br>