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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 80 (estimated) |
| Sponsor | Queen Mary University of London Academic / other |
| Locations | 1 site (London) |
| Status | Recruiting |
| Started | April 1, 2025 |
| Main results expected | September 4, 2026 |
| Study ends | September 4, 2026 |
| Registry record updated | May 19, 2026 |
| Trial ID | NCT06887387 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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.