Actively Recruiting

Age: 18Years +
All Genders
ID04437914

Accuracy of Cardiac Arrhythmias and Conduction Disorders Diagnosis Using Smartwatch Compared to Conventional Electrocardiogram in Patients With Cardiovascular Disease

Led by Federal University of Piaui · Updated on 2024-09-25

110

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Accuracy of Cardiac Arrhythmias and Conduction Disorders Diagnosis Using a Smartwatch

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with one or more of the following: systemic arterial hypertension, heart failure, valve disease, coronary atherosclerotic disease, myocardial infarction, endocarditis, myocarditis, diabetes, cardiac arrhythmias
  • Patients with cardiac pacemakers or implantable automatic defibrillators
  • Followed up in cardiology, hospitalized or outpatient
Not Eligible

You will not qualify if you...

  • Electrocardiographic tracings from the watch or conventional ECG of poor quality making diagnosis impossible or difficult
  • Withdrawal of consent by the patient or legal guardian

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

Trial Site Locations

Total: 1 location

1

Carlos Eduardo B. de Lima

Teresina, Piauí, Brazil, 64048-350

Actively Recruiting

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Research Team

C

Carlos Eduardo B. Lima, MD, PhD

C

Carlos Eduardo B. Lima, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial