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Detection of Atrial Fibrillation Using PPG From Smartphone Cameras

RECRUITINGSponsored by Happitech BV
Actively Recruiting
SponsorHappitech BV
Started2026-06-30
Est. completion2026-11
Eligibility
Age22 Minutes+
Healthy vol.Accepted
Locations4 sites

Summary

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

Age: 22 Minutes+Healthy volunteers accepted
Inclusion Criteria:

1. Adults aged 22 years or older
2. Owns a smartphone and knows how to operate and navigate different applications.
3. Individuals able to read, understand, and sign the consent form.
4. Cardiology patients consulting the cardiac outpatient clinic.
5. History of persistent AF or other cardiac rhythm

Exclusion Criteria:

1. Participants with cognitive impairments
2. Individuals who cannot read, speak, and/or understand English
3. 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

Conditions2

Atrial Fibrillation (AF)Heart Disease

Locations4 sites

Arkansas

1 site
Nair Research, LLC dba Arrhythmia Research Group LLC
Jonesboro, Arkansas, 72401
Kayla Rubino870-340-7387krubino@drnairresearch.com

Colorado

1 site
South Denver Cardiology
Littleton, Colorado, 80210
Kathy Siegel, Clinical Research Director720-217-6139ksiegel@southdenver.com

Louisiana

1 site
Tulane University
Kunal Sameer, Associate Director of Ops203-285-5666ksameer@tulane.edu

Oklahoma

1 site
CardioVascular Health Clinic
Sophie Haynes, Regulatory Director405-696-0007sophie@hightowerclinical.com

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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