Monitoring of patients with chronic heart failure with a wrist-worn data logger.
Recruiting
- Conditions
- Heart failure regardless of etiology and heart failure type
- Registration Number
- NL-OMON21559
- Lead Sponsor
- Máxima Medical Centre, Eindhoven/Veldhoven, The Netherlands
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
1. Diagnosed with heart failure (regardless of heart failure type and etiology)
2. Admitted to the hospital due to acute decompensated heart failure
3. Age = 18 years
4. Able to speak and read the Dutch language
5. Willing and able to provide informed consent
Exclusion Criteria
1. Permanent atrial fibrillation
2. Not able or willing to wear a wrist-worn data logger on a daily basis (for example due to work related obligations)
3. Major planned (cardiac) surgery in the upcoming 3 months
4. Not able to perform daily physical activity due to orthopedic of neurological disease
5. Bed/chair ridden patients
6. Presence of wounds, injuries or infectious diseases on the skin where the wrist-wearable device will be placed
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the predictive value of different physical activity parameters, measured with a wrist-worn data logger, in deterioration of heart failure.
- Secondary Outcome Measures
Name Time Method