Clinical trial Recruiting at 1 site Observational Ages 18 and up

Monitoring Long QT Syndrome with Wearable Devices

Official title: Application of Wearable Devices for Remote QT Interval Monitoring and Symptom Investigation for Patients With Long QT Syndrome

Run by Queen Mary University of London · NCT06887387 · Data updated 2026-11-12

This study tests if using wearable devices to track heart activity can help adults with Long QT syndrome manage their condition better.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment80 (estimated)
SponsorQueen Mary University of London
Academic / other
Locations1 site (London)
StatusRecruiting
StartedApril 1, 2025
Main results expectedSeptember 4, 2026
Study endsSeptember 4, 2026
Registry record updatedMay 19, 2026
Trial IDNCT06887387 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and over who have been clinically diagnosed with Long QT syndrome.

Probably not a fit

Patients who are unwilling or unable to provide informed consent or have specific cardiac conditions may 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 observational study investigates the effectiveness of wearable devices in monitoring patients diagnosed with Long QT syndrome. Participants will be equipped with these devices to track their heart activity and other relevant health metrics. The study aims to determine if continuous monitoring can improve patient outcomes and provide valuable data for managing this condition. Eligible participants must be 18 years or older and have a clinical diagnosis of Long QT syndrome.

Why it matters

Potential benefit: If successful, this study could enhance the management and monitoring of patients with Long QT syndrome, potentially leading to better health outcomes.

How similar studies have gone: While the use of wearable devices for monitoring various health conditions is gaining traction, the specific application in Long QT syndrome is relatively novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
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 Criteria:

* Unwilling or unable to give consent
* Ventricular pacing at recruitment
* Bundle branch block or pre-excitation at baseline

Where it's running

  • Barts and London Hospital NHS Trust
    London, United Kingdom
    Recruiting

Study contacts

  • Principal investigator: William J Young, MBBS, PhD — Queen Mary University of London and St Bartholomew's Hospital

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.
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.