The effects of a mobile telemonitoring guided cardiac rehabilitation programme (mCR) versus no cardiac rehabilitation in elderly patients in Europe.
Completed
- Conditions
- Cardiac rehabilitation, eHealth
- Registration Number
- NL-OMON24643
- Lead Sponsor
- Isala Zwolle
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 238
Inclusion Criteria
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
-Patients of 65 years or older who are a candidate for CR and non-voluntary to participate in the regular CR programme
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
-Contraindication to CR
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in peak oxygen uptake (VO2peak) between the end of CR programme (T1) and baseline (T0).
- Secondary Outcome Measures
Name Time Method oDifference in VO2peak between 12 months (T2) and T0<br /><br>oDifference in VO2peak between T2 and T1<br /><br>oTraditional risk factors for CVD<br /><br>oMajor Adverse Cardiovascular Events (MACE)<br /><br>oGeneral health<br /><br>oCare utilisation<br /><br>oCosts of care utilisation <br /><br>oAdherence<br /><br>oCompliance<br />