Wearable Devices for Patient Monitoring in Long QT Syndrome

Last updated: May 15, 2025
Sponsor: Queen Mary University of London
Overall Status: Active - Recruiting

Phase

N/A

Condition

Arrhythmia

Dysrhythmia

Cardiac Disease

Treatment

Wearable device

Clinical Study ID

NCT06887387
173178
  • Ages > 18
  • All Genders

Study Summary

The main research question of this study is whether wearable devices have utility in monitoring patients with Long QT syndrome.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Clinical diagnosis of Long QT Syndrome

  • Aged 18 years or over

  • Phone with iOS version 15 or Android OS 9.0 or higher

  • Able and willing to provide informed consent

Exclusion

Exclusion Criteria:

  • Unwilling or unable to give consent

  • Ventricular pacing at recruitment

  • Bundle branch block or pre-excitation at baseline

Study Design

Total Participants: 80
Treatment Group(s): 1
Primary Treatment: Wearable device
Phase:
Study Start date:
April 01, 2025
Estimated Completion Date:
September 04, 2026

Connect with a study center

  • Barts and London Hospital NHS Trust

    London,
    United Kingdom

    Active - Recruiting

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