Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Withings
Age
22–any
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Male or female who are 22 years of age or older
Subject able to read, understand, and provide written informed consent
Subject willing and able to participate in the study procedures as described in the consent form
Subject able to communicate effectively with and willing to follow instructions from the study staff
You may not be if
Subject with an implanted electrical device (i.e. pacemaker, ICD …), whether active or inactive
Pathologic disorders that may affect motricity resulting in significant hands tremor that prevents subject from being able to hold still (e.g. Parkinson disease)
Myocardial Infarction (MI) within 90 days prior to the enrollment
Pulmonary embolism or pulmonary infarction within 90 days prior to the enrollment
Stroke or Transient Ischemic Attack (TIA) within 90 days prior to the enrollment
Active or history of life-threatening rhythms as determined by investigators (e.g. ventricular tachycardia, ventricular fibrillation, 3rd degree heart block)
Any cardiovascular disease that investigators would consider as a risk to subject or renders data uninterpretable (e.g. recent or ongoing unstable angina, decompensated heart failure, active myocarditis or pericarditis)
Active or symptomatic skin disease on Schiller electrode attachment sites or fingertips which would be in contact with BeamO electrodes (e.g. eczema, rosacea, impetigo, dermatomyositis or allergic contact dermatitis)
Known sensitivity to medical adhesives, isopropyl alcohol,, electrocardiogram (ECG) electrodes, including known allergy or sensitivity to stainless steel (used in BeamO electrodes).
Clareo Health | WIBOFA - Validation of SCT02 With ECG-App for Detection of AF
