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)

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) - HIIT-OXI-NIBP-POS

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON56499

Enrollment

Registered

2024-01-22

Start date

2024-01-29

Completion date

Unknown

Last updated

2024-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

n.v.t.

Interventions

None listed

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 18 years old or above, able to provide consent, able to preform a HIIT

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Root mean squared error between measurements (heart rate, SpO2 and respiration rate) recorded by Corsano Cardiowatch 87-2 and reference device.	—

Secondary

Measure	Time frame
Arithmetic mean and standard deviation of the error between blood pressure values measured by the Corsano Cardiowatch 287-2 and the reference method according to ISO 81060-2:2019.	—

Countries

Netherlands

Outcome results