Quality assessment of an integrated care pathway using telemonitoring in patients with chronic heart failure and COPD
Recruiting
- Conditions
- Chronic heart failureCOPD1001928010006436
- Registration Number
- NL-OMON54683
- Lead Sponsor
- Maxima Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 23
Inclusion Criteria
1. Patients diagnosed with both CHF (HFrEF, HFpEF or HFmrEF) and COPD
regardless of aetiology
2. At least one hospital admission during the last year (due to CHF/COPD)
3. Age >= 18 year
4. Able to speak and read the Dutch language
5. Life expectancy > 2.5 years
6. Sufficient digital skills (or caregiver)
Exclusion Criteria
The patient does not have internet connection
Having a psychological disorder preventing participation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The primary endpoint is to investigate whether TM in patients with combined CHF<br /><br>and COPD results in a delayed decline or improved quality of life (EQ-5D), as<br /><br>compared to usual care</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary endpoints are:<br /><br>1. To investigate whether TM in patients with combined CHF and COPD results in<br /><br>a delayed decline or improved HRQoL (MLHFQ, SGRQ).<br /><br>2. To investigate whether TM results in improved levels of self-management as<br /><br>compared to usual care (PAM13).<br /><br>3. To investigate patient satisfaction with TM compared to usual care (PREM)<br /><br>4. To investigate whether patients are compliant to the TM program.<br /><br>5. To assess health-care costs of TM compared with usual care. </p><br>