This study has the following objective: • To validate the capability of the μ-Cor System to monitor ECG, Heart Rate (HR), Respiration Rate (RR), Posture and Activity in healthy human subjects. The μ-Cor validation will be demonstrated at two body locations: 1. Side location (below left armpit) for study arm 1, and 2. Front location (upper left chest) for study arm 2 An FDA-cleared comparator device will be used to support the validation of the study device.
This study has the following objective: • To validate the capability of the μ-Cor System to monitor ECG, Heart Rate (HR), Respiration Rate (RR), Posture and Activity in healthy human subjects. The μ-Cor validation will be demonstrated at two body locations: 1. Side location (below left armpit) for study arm 1, and 2. Front location (upper left chest) for study arm 2 An FDA-cleared comparator device will be used to support the validation of the study device.
Study Type
OBSERVATIONAL
Enrollment
30
Respiratory rate
The difference between the μCor RR and the comparator RR will be lower than 2.8bpm (STD).
Time frame: Immediately
Posture
90% agreement between the positions (supine / reclined / upright) derived from μCor reporting and the known position
Time frame: Immediately
Activity
μCor output is provided as "active" and "not active". 90% correct classification of activity will be required of recordings.
Time frame: Immediately
Heart Rate
Time frame: Immediately
ECG
Time frame: Immediately
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