Enhancing Knowledge Implantable Cardioverter-Defibrillators (ICDs)
NCT00822965 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 104
Last updated 2016-01-07
Summary
The specific aims of the patient intervention are to:
1. increase patient knowledge about pacemakers (PM) and implantable cardioverter-defibrillators (ICDs)
2. help patients to identify if their PM or ICD has been interrogated
3. improve patient's physician-patient communication skills
4. teach patients how to identify if their device has been recalled
5. train patients what to do in case of a device recall
The educational interventions proposed, if proven to be effective by this pilot, will provide a low-cost, reproducible intervention to improve the clinical care and safe management of pacemakers (PM) and implantable cardioverter-defibrillators (ICD) in patients. The goal of the intervention will be to promote the safe use of implantable pulse generators.
Conditions
- Pacemaker
- Implantable Cardioverter-Defibrillators
Interventions
- OTHER
-
Questionnaires
3 sets of questionnaires at the beginning of the study, at 2-months and at 4-months.
- OTHER
-
Phone Interviews
2 follow-up phone interviews.
- BEHAVIORAL
-
Educational Packet
Video or DVD of device information, updates, recalls, on-line resources and benefits of routine follow-up for device(s).
Sponsors & Collaborators
-
Mike Hogg Foundation
collaborator UNKNOWN -
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
Maria Suarez-Almazor, MD, PhD · M.D. Anderson Cancer Center
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-01-31
- Primary Completion
- 2015-01-31
- Completion
- 2015-01-31
Countries
- United States
Study Locations
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