Barriers to Use of Remote Monitoring in Patients With Implantable Cardioverter Defibrillators
Completed · Not applicable
Conditions studied: Cardiac Patients, Implantable Cardioverter Defibrillator
In brief
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.
Key facts
- Study ID
- NCT02361333
- Run by
- Yale University
- People needed
- 20
- Starts
- 2012-10-01
- Expected to finish
- 2014-10-01
- Last updated by the study team
- 2018-01-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Less than 18 years of age
- From a vulnerable population
- Incompetent/suffers from dementia
- Non-English speaking
Where it is running
- Yale Electrophysiology — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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