Randomised Controlled Trial for an e-Health application in EUropean Cardiac Rehabilitation programmes in Elderly; Assessment of the effects on sustainablity and participation level of a mobile telemonitoring guided cardiac rehabilitation programma (mCR) and its cost effectiveness, in elderly patients in Europe

Completed

• Conditions: cardiovascular disease; heart disease; 10028593

• Registration Number: NL-OMON42642
• Lead Sponsor: Isala Klinieken

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: 48

Inclusion Criteria

- Patients of 65 years or older who are a candidate for CR and non-voluntary to
participate in the regular CR programme
- Signed written informed consent
- One of the following criteria:
o Patients with an acute coronary syndrome, including myocardial infarction (MI) and/or revascularisation
within 3 months prior to the start of the CR programme
o Patients that underwent a percutaneous coronary intervention (PCI) within 3
months prior to the start of the CR programme
o Patients that received coronary artery bypass grafting (CABG) within 3 months
prior to the start of the CR programme

Exclusion Criteria

- Contraindication to CR
- Mental impairment leading to inability to cooperate
- Severe impaired ability to exercise
- Signs of severe cardiac ischemia and/or a positive exercise testing on severe cardiac ischemia
- Insufficient knowledge of the native 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>Difference in peak oxygen uptake (VO2peak) between the end of CR programme (T1)<br /><br>and baseline (T0)</p><br>