MedPath

Patient Expectations After Implantable-cardioverter Defibrillator (ICD) Implantation

Completed
Conditions
Defibrillators, Implantable
Registration Number
NCT00845390
Lead Sponsor
University of California, San Francisco
Brief Summary

This study will be a qualitative survey to understand the expectations of defibrillator patients with regards to their device. It is unknown what ICD (implantable-cardioverter defibrillator) patients understand about their device and its purpose, thus we will be talking to them about their device. Also, we will be interested in studying their beliefs on how the ICD impacts their life expectancy and quality of life.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • All patients are eligible for inclusion. We hope to acquire a wide range of ages but are not limited to a specific set.
Read More
Exclusion Criteria
  • Non-English speakers will be excluded.
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Why did you have an ICD implanted?after ICD implantation
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UCSF Arrhythmia and Device Clinic

🇺🇸

San Francisco, California, United States

© Copyright 2025. All Rights Reserved by MedPath