Video-based Detection of Atrial Fibrillation

University of Rochester

Status

Completed

Conditions

Atrial Fibrillation

Treatments

Diagnostic Test: Facial video of detection of cardiac disease

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT04267133

68409

Details and patient eligibility

About

The project focuses on the evaluation of a novel, contactless monitoring technology to measure the blood pulsatile signal based on the video recording of an individual's face. The variability of the pulse rate is computed to identify the presence of atrial fibrillation (AF). We propose to enroll 315 patients with symptomatic AF, paroxysmal or persistent, who go through successful radiofrequency ablation or electrical cardioversion. A computer tablet will be used by the subjects at home during 14 days after their procedure to read emails, browse the internet and watch videos. Facial video recordings will be automatically acquired during these daily activities by the tablet device. The subject will be wearing an ECG patch during the follow-up period. The one-lead continuous ECG will be used as a reference to verify the presence of AF rhythm during facial video recordings. The primary aim of the study is to demonstrate the validity and robustness of the video-based technology to detect the presence of AF when facial videos are acquired by the patients at home.

Enrollment

256 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Men and women older than 18 years of age,
Medically-managed for symptomatic AF (persistent or paroxysmal),
In sinus rhythm after their ablation procedure,
In sinus rhythm after trans-thoracic electrical cardioversion.

Exclusion criteria

Implanted with a device (pacemaker, CRT, ICD) and a ventricular pacing requirement superior or equal to 70%,
Known allergic reaction to adhesives or hydrogels or with a family history of adhesive skin allergies,
Unable to cooperate with the protocol due to dementia, psychological, or other related reason,
Refusing to sign the consent for participation,
Unable to operate the device such as blind patients.
Patients with Parkinson disease (or other central nervous system disorder/Tremor) who cannot record a stable video signal of their face.
The subject was previously enrolled in the current study.
The subject wears clothing covering the face, or uses facial makeup that will interfere with the quality of facial recordings.
Subject does not have internet access at home and lacks the technology to participate.