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Effect of Wearable Devices on Patient-Reported Outcomes and Clinical Utilization: A Randomized, Controlled Trial

Overview

Información sobre este estudio

The purpose of this study is to help researchers better understand the impact of wearable devices on patient experience and clinical trends following a cardioversion.

 

 

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Age ≥ 22 years old.
  • English-speaking.
  • Planned for outpatient direct current cardioversion for atrial fibrillation or atrial flutter.
  • Participant is willing and able to read and sign consent and participate in study.
  • Participant lives independently and does not require continuous care.
  • Participant has an email account (or is willing to create one).
  • Participant has a compatible smartphone (iPhone 6s or later).
  •  
  • Participant is willing to wear only the device they are randomized to receive for the study period for as many hours during the day as they are able, except for the time spent charging the device or in the environments that may be suboptimal for the device.
  • Participant is willing to use the Hugo mobile health platform and Apple Watch Series 5 or Withings Move.
  • Participant has cardiology care at Mayo Clinic and primary care in a health system with a patient portal.

Exclusion Criteria:

  • Do not meet all inclusion criteria as listed above
  • Unable to provide informed consent.

Eligibility last updated 1/24/22. Questions regarding updates should be directed to the study team contact.

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Peter Noseworthy, M.D., M.B.A.

Cerrado para la inscripción

Contact information:

Lindsay Emanuel

(507) 422-6300

Emanuel.Lindsay@mayo.edu

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20490363

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