Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02361333
Other study ID # 1208010730
Secondary ID
Status Completed
Phase N/A
First received January 20, 2015
Last updated January 12, 2018
Start date October 2012
Est. completion date October 2014

Study information

Verified date January 2018
Source Yale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date October 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Teaching Intervention
Patients will be taught how to install and use a remote monitor

Locations

Country Name City State
United States Yale Electrophysiology New Haven Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Yale University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of remote Transmissions of data using remote monitor made by patient 6 months
See also
  Status Clinical Trial Phase
Terminated NCT02916550 - Breathing Intervention for Cardiac Anxiety N/A
Terminated NCT01464476 - Efficacy and Safety Study of Azimilide on the Incidence of Cardiovascular Hospitalizations/Emergency Department Visits or Cardiovascular Death in Patients With an Implantable Cardioverter Defibrillator (ICD) (SHIELD-2) Phase 3
Recruiting NCT01378572 - Electrophysiologic and Morphologic Assessment of the Substrate to Guide Implantation of Defibrillators in Dilated Cardiomyopathy N/A
Terminated NCT03590730 - Benefits of ICD for the Primary Prevention in Patients With Valvular Cardiomyopathy
Completed NCT01459874 - Evaluation of an Organizational Model for Remote Monitoring of Pacemaker and Implantable Cardioverter Defibrillator Recipients N/A
Recruiting NCT05373940 - Cardioverter DefIbriIlator PlacEMent for priMary Prevention of Sudden cArdiac Death in Patients Older Than 75 Years N/A
Completed NCT02341768 - Clinical and Device Functional Assessment of Real World ICD Patients
Recruiting NCT03932604 - Atrial Sensing Capability for Better Detection of Atrial Fibrillation N/A
Completed NCT02088619 - Positive Therapy for Autonomic Function & Mood in ICD Patients N/A
Completed NCT02318550 - Registry of Patients for MRI With Non-MRI Conditional Pacemakers and ICD Non-MRI Conditional Pacemakers and ICD