MedPath

Implantable Cardioverter-Defibrillator Use in the VA System

Phase 3
Completed
Conditions
Cardiomyopathies
Interventions
Behavioral: Clinical Reminder
Registration Number
NCT01217827
Lead Sponsor
Stanford University
Brief Summary

Despite being a proven life-saving intervention in appropriately selected individuals, multiple studies continue to demonstrate low implantation of defibrillators in potential candidates. Based upon prior research, a major barrier to low utilization is low referral of potential candidates by healthcare providers. In this study, via brief clinical reminder placed in the electronic medical record, we ask healthcare providers who have not referred potential candidates for defibrillator the reasons for this decision and provide them with the tools for referral if appropriate.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
89
Inclusion Criteria

Meeting published criteria for receipt of an implantable cardioverter defibrillator

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Exclusion Criteria

provider is not affiliated with the VA health care system

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Clinical ReminderClinical ReminderReminder of potential candidacy for an implantable cardioverter defibrillator. The reminder is placed in the medical record with copy to the primary provider and any cardiologist managing the patient.
Primary Outcome Measures
NameTimeMethod
Referral for Implantable Cardioverter Defibrillator6 months

Referral of the patient to electrophysiology clinic for evaluation for cardioverter defibrillator implantation.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

VA Palo Alto Health Care System

🇺🇸

Palo Alto, California, United States

Stanford University School of Medicine

🇺🇸

Stanford, California, United States

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