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Wearable Devices for Patient Monitoring in Long QT Syndrome

Q

Queen Mary University of London

Status

Enrolling

Conditions

Long QT Syndrome

Treatments

Device: Wearable device

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

80 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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