Randomized clinical trial for an extended cardiac rehabilitation program using telemonitoring

Completed

• Conditions: cardiovascular disease; heart disease; 10028593

• Registration Number: NL-OMON41024
• Lead Sponsor: niversitair Medisch Centrum Sint Radboud

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

- Patients participating in cardiac rehabilitation (minimal attendance of 80% in physical program)
- Signed written informed consent
- One of the following criteria:
o Patients with an acute coronary syndrome, including myocardial infarction (MI) within 3 months
prior to start cardiac rehabilitation program
o Patients that underwent a percutaneous coronary intervention (PCI) within 3 months prior to
prior to start cardiac rehabilitation program
o Patients that received coronary artery bypass grafting (CABG) within 3 months prior to start
cardiac rehabilitation program

Exclusion Criteria

- Contraindication to cardiac rehabilitation
- Mental impairment leading to inability to cooperate
- Severe impaired ability to exercise
- Signs of cardiac ischemia and/or a positive exercise testing on cardiac ischemia
- Insufficient knowledge of the Dutch language
- No access, availability or insufficient knowledge of a computer with internet
- Implanted cardiac device (pacemaker, ICD)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Main study parameter/endpoint is physical fitness defined by peak oxygen uptake<br /><br>obtained from an incremental maximal cycle ergometer exercise test at 12<br /><br>months. </p><br>