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Clinical trial Recruiting at 1 site Interventional

Using a connected watch to record ECG traces

Official title: Feasibility and Diagnostic Relevance of Recording an ECG Trace With a Connected Watch

Run by University Hospital, Bordeaux · NCT06272396 · Data updated 2026-11-12

This study is testing if a connected watch can accurately record heart activity compared to traditional heart monitors in people with different heart conditions.

Quick facts

Study typeInterventional
SexAll
Enrollment3000 (estimated)
SponsorUniversity Hospital, Bordeaux
Academic / other
Locations1 site (Pessac)
StatusRecruiting
StartedMarch 26, 2024
Main results expectedMarch 26, 2027
Study endsMarch 26, 2028
Registry record updatedApril 2, 2025
Trial IDNCT06272396 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients hospitalized or consulted at the Haut Lévêque cardiology hospital, regardless of age, who can provide informed consent.

Probably not a fit

Patients who are unable to give consent or are under legal protection measures will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of ECG recordings from a connected watch compared to standard 12-lead ECGs in patients with various heart conditions. It aims to assess the sensitivity of 1D and 6D ECG recordings in measuring electrical parameters of the heart. Additionally, the study will create a database of ECG tracings to develop and validate an artificial intelligence algorithm for automatic ECG analysis. The participants will include both healthy individuals and those with arrhythmias or other cardiac issues.

Why it matters

Potential benefit: If successful, this study could enhance remote monitoring of heart conditions, leading to quicker and more accurate diagnoses.

How similar studies have gone: Other studies have shown promise in using wearable technology for ECG monitoring, indicating a growing interest and potential in this area.

Who can join: the full rules

Show full inclusion / exclusion criteria 
Inclusion Criteria:

* Patients hospitalized or seen in consultation in one of the departments of the Haut Lévêque cardiology hospital,
* Patient of both sexes, minor (from birth to 18 years) or adult,
* Free, informed and written consent from the patient or, in the case of minors, from the legal parent (at the latest on the day of inclusion and before any examination required for the research),
* Subject affiliated to or benefiting from a social security regime.

Exclusion Criteria:

* Person incapable of giving consent,
* Person subject to a legal protection measure (safeguard of justice, tutorship or curatorship),
* A person deprived of liberty by judicial or administrative decision.

Where it's running

  • Hôpital Haut-Lévèque
    Pessac, France     Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Arrhythmias, Cardiac 24University Hospital, Bordeaux 113
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.