Pulse Rate/SPO2/Respiration Rate/RR-intervals/Blood Pressure/Device Position Test for Corsano CARDIOWATCH 287-2 during High Intensity Interval Training: an Evaluation Study (HIIT-OXI-NIBP-POS)
Phase 4
Completed
- Conditions
- n.v.t.10007521
- Registration Number
- NL-OMON56499
- Lead Sponsor
- Corsano Health B.V.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 35
Inclusion Criteria
18 years old or above, able to provide consent, able to preform a HIIT
Exclusion Criteria
Injuries or unable to perform HIIT, unable to wear the Corsano CardioWatch
287-2 due to reasons such as allergic reactions, wounds, amputations etc.,
unable to sign informed consent, baseline SBP > 160 mmHg and/or baseline DBP >
100 mmHg, high total cardiovascular risk, pregnant or breastfeeding.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Root mean squared error between measurements (heart rate, SpO2 and respiration<br /><br>rate) recorded by Corsano Cardiowatch 87-2 and reference device.</p><br>
- Secondary Outcome Measures
Name Time Method <p>Arithmetic mean and standard deviation of the error between blood pressure<br /><br>values measured by the Corsano Cardiowatch 287-2 and the reference method<br /><br>according to ISO 81060-2:2019.</p><br>