Detection of Atrial Fibrillation Using PPG From Smartphone Cameras
ConditionAtrial Fibrillation (AF)
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age22+
SponsorHappitech BV
About this trial
The protocol is designed to enroll patients from at least 3 diverse clinical sites with smartphones who are being evaluated for the presence or absence of atrial fibrillation (AF) using the Heart Rhythm Software algorithm running on their smartphones. Algorithm output will be compared to a gold standard of 12-lead ECG recorded with a simultaneous PPG measurement.
Eligibility criteria
Qualifiers
Adults aged 22 years or older
Owns a smartphone and knows how to operate and navigate different applications.
Individuals able to read, understand, and sign the consent form.
Cardiology patients consulting the cardiac outpatient clinic.
Disqualifiers
Participants with cognitive impairments
Individuals who cannot read, speak, and/or understand English
Patients with implantable neurostimulators, cardiac implantable device in an atrial or ventricular paced rhythm documented on a 12-lead ECG during the initial study visit
Trial design
Treatments tested in this trial
- 12 Lead ECG is compared to a smartphone based PPG
Treatment groups
554 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov