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Comparison of QT Interval Readings Between Smartwatch Combined With Cardiologs Artificial Intelligence and 12-lead ECG

Comparison of QT Interval Readings Between Smartwatch Combined With Cardiologs Artificial Intelligence and 12-lead ECG in Subjects Hospitalized for Antiarrhythmic Drug Initiation and Follow-up

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05161065
Enrollment
50
Registered
2021-12-16
Start date
2022-02-12
Completion date
2023-02-28
Last updated
2023-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Brief summary

The WatchQT study will compare the performance of a smartwatch combined with Cardiologs ECG AI Analysis system in monitoring corrected QT (QTc) intervals with that measured on a manually read 12-lead ECG in subjects with Normal Sinus Rhythm (NSR) during antiarrhythmic drug (AAD) initiation and follow-up at the hospital.

Detailed description

The WatchQT Study is a prospective, non-significant risk, non-randomized, monocentric, open, comparative, concordance pilot study. Under subject consent, subjects hospitalized for AAD initiation and monitoring will have smartwatch ECG recordings done simultaneously with 12-lead ECG measurements before and after drug administration twice a day, in accordance with the existing in-stay subject monitoring protocol.

Interventions

Apple Watch recordings interpreted by Cardiologs AI done simultaneously with each 12-lead ECG

Sponsors

Cardiologs Technologies
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Subjects over 22, able and willing to participate in the study 2. Subjects who are admitted to the hospital in NSR or AF and are eligible for AAD (class Ia or class III) dose initiation or re-initiation. 3. Subjects having read the patient information letter and provided his/her consent to participate in writing, by dating and signing the informed consent prior to any trial-related procedure being conducted

Exclusion criteria

1. Subjects with Cardiac Implantable Electronic Devices (CIED) 2. Pregnant or breast-feeding subjects

Design outcomes

Primary

MeasureTime frameDescription
Concordance between QTc intervals (in ms) measured by smartwatch combined with Cardiologs AI and that measured by manually read 12-lead ECGReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationConcordance between QTc intervals measured by smartwatch combined with Cardiologs AI and that measured by manually read 12-lead ECG for each measurement done during NSR. The Bazett (QTcB in ms) and Fridericia (QTcF in ms) methods will be used to correct QT intervals

Secondary

MeasureTime frameDescription
Concordance between QTcB and QTcF intervals measured by the different methodsReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationConcordance between QTcB and QTcF intervals measured by the different methods (smartwatch combined with Cardiologs AI, smartwatch read manually, 12-lead read manually, lead 1 from 12-lead read manually and automated interpretation of the 12 lead ECG machine)
Description of the QTc interval measurements in NSRReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationDescription of the QTc interval measurements in NSR as a function of timepoints by the different methods
Quantitative analysis to determine the interobserver variabilityReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationQuantitative analysis to determine the interobserver variability in QTc interval measurements by the smartwatch and 12-lead ECG manual readings
Description of the sensitivity and specificity of the smartwatch combined with Cardiologs AIReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationDescription of the sensitivity and specificity of the smartwatch combined with Cardiologs AI in determining subjects at risk of AAD induced ventricular arrhythmia compared to that identified by manually read 12-lead ECG in subjects with a prolonged QTc \> 500 ms and/or subjects with a QTc prolongation of \> 15% after their initial AAD dose
Descriptive analysis of QT interval measurements in AF measured by smartwatch combined with Cardiologs AI and manually read 12-lead ECGReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalization.Descriptive analysis of QT interval measurements in AF measured by smartwatch combined with Cardiologs AI and manually read 12-lead ECG at each timepoint and overall.
Analysis of QT interval measured in subsets of subjects with and without wide QRSReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationPatient with wide QRS is determined as a QRS\>120ms at D0 from automated interpretation of the 12-lead ECG machine. The analysis will be done in subset of 2 groups according to the QRS measured as wide or not machine
Description of the QT interval defined as uncertain by the smartwatch combined with Cardiologs AIReadings taken simultaneously right before and 2-3 hours after drug administration during hospitalizationDescription of the QT interval defined as uncertain by the smartwatch combined with Cardiologs AI

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026