Triggers and Risk Factors for Recurrence of Atrial Arrhythmias With the Use of Long-term Monitoring

Active, not recruitingOBSERVATIONAL
Enrollment

182

Participants

Timeline

Start Date

August 1, 2021

Primary Completion Date

July 15, 2024

Study Completion Date

September 30, 2024

Conditions
Atrial FibrillationAtrial FlutterAtrial ArrhythmiaAtrial TachycardiaPremature Atrial ContractionsArterial HypertensionSleep DisorderSleep ApneaStressPhysical InactivityOverexertionAlcohol DrinkingCaffeine Dependence
Interventions
DEVICE

Devices for long-term monitoring of objective and subjective parameters of the body

Patients will use a 1-lead Holter ECG (Bittium Faros) for heart rhythm and physical activity analysis, a wearable wrist-worn device with photoplethysmography and 6-lead ECG for heart rhythm analysis, a sleep tracking mat (Withings sleep analyser) for sleep analysis, a smartphone with triggers application for entering the subjective triggers (stress, coffee, alcohol intake and others), a 48-hour ambulatory blood pressure monitor for 2 days and a regular blood pressure monitor for up to 5 days. Patients will be monitored for up to 7 days with the described system of devices. In addition, patients will receive investigations of heart echocardiography, laboratory tests and surveys to evaluate the system and the use of acquired information.

Trial Locations (1)

Unknown

Vilnius University Santaros Clinics, Vilnius

All Listed Sponsors
collaborator

Kaunas University of Technology

OTHER

lead

Vilnius University

OTHER