Silent Atrial Fibrillation in Elderly Pacemaker Users: A Randomized Trial Using Home Monitoring.
Ceb Lima, M Martinelli, G L Peixoto...
https://pubmed.ncbi.nlm.nih.gov/26413928Actively Recruiting
Led by Federal University of Piaui · Updated on 2024-09-25
110
Participants Needed
1
Research Sites
43 weeks
Total Duration
Researchers are investigating how accurately a smartwatch can detect heart rhythm and conduction problems in patients with cardiovascular diseases. This observational study compares the heart readings from a smartwatch to those from a traditional 12-lead electrocardiogram (ECG) to see how similar the results are and how well the smartwatch's automatic diagnosis matches expert assessments. The study aims to improve early detection and monitoring of heart conditions to prevent serious health issues. Participants will have their heart activity recorded using an Apple Watch Series 4 and a conventional ECG device. The smartwatch will record two 30-second ECG tracings while the patient is at rest, attached to the left wrist with the right hand touching the sensor to complete the measurement. The conventional ECG will capture 12 leads including a 30-second rhythm trace. The smartwatch's automatic diagnoses will be compared with the conventional ECG results and interpreted by two independent cardiologists. During the study, participants provide clinical and demographic information and undergo both smartwatch and conventional ECG recordings. The researchers will analyze the similarity of heart rate, waveforms, and intervals between methods, along with the diagnostic accuracy of atrial fibrillation and other heart rhythm disorders. The main outcome is the agreement between the smartwatch and conventional ECG diagnoses. Safety and data quality will be monitored, and participants may withdraw at any time without affecting their medical care. The total study duration is around 30 days for outcome assessment.
CONDITIONS
Accuracy of Cardiac Arrhythmias and Conduction Disorders Diagnosis Using a Smartwatch
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day assessment
Participants undergo electrocardiographic recordings using both a smartwatch and a conventional 12-lead ECG to compare diagnostic accuracy of cardiac arrhythmias and conduction disorders.
1 visit (in-person)
Duration - 30 days
Participants' diagnostic results are analyzed and correlated over a 30-day period to assess the accuracy and reliability of the smartwatch electrocardiogram compared to conventional methods.
No additional visits; remote monitoring
Total: 1 location
1
Carlos Eduardo B. de Lima
Teresina, Piauí, Brazil, 64048-350
Actively Recruiting
C
Carlos Eduardo B. Lima, MD, PhD
C
Carlos Eduardo B. Lima, MD, PhD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Ceb Lima, M Martinelli, G L Peixoto...
https://pubmed.ncbi.nlm.nih.gov/26413928