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OpenTrials
Completed

NCT Number: NCT02361333

Barriers to Use of Remote Monitoring in Patients With Implantable Cardioverter Defibrillators

The purpose of this study is to determine whether a teaching intervention can help increase the use of remote monitors in patients with implantable cardioverter defibrillators.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yale Electrophysiology

New Haven, Connecticut, 06511, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Received a Medtronic implantable cardioverter defibrillator (ICD) at Yale Electrophysiology, between January 2007 and June 2012
  • ICD is compatible with Carelink, Medtronic's remote monitoring system

Exclusion criteria

  • Less than 18 years of age
  • From a vulnerable population
  • Incompetent/suffers from dementia
  • Non-English speaking

Treatment and study plan

Teaching intervention

Behavioral

Patients will be taught how to install and use a remote monitor

Primary outcomes

  1. Number of remote Transmissions of data using remote monitor made by patient

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Yale University

Other

Registry information

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Feb 11, 2015
Registry last updated
Jan 17, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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