Skip to main content
Clinical Trials/NCT02888028
NCT02888028
Completed
Not Applicable

Quality of Life and Device Acceptance in Patients With Implantable Cardioverter-defibrillators Undergoing Remote ICD Follow-up

LMU Klinikum2 sites in 1 country182 target enrollmentMay 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anxiety
Sponsor
LMU Klinikum
Enrollment
182
Locations
2
Primary Endpoint
Influence of ICD remote monitoring on Quality of Life, measured by the EQ5D questionnaire
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study investigates whether an additional remote follow-up of patients with implantable cardioverter-defibrillators (ICDs) has beneficial effects on Quality of life (QoL), levels of anxiety and depression and device acceptance. Patients are randomized to either conventional in-office FU only or additional remote surveillance, follow-up duration is 12 months. The influence of other variables (age, sex,..) is evaluated regarding their influence on study endpoints.

Detailed Description

The rising number of implantable cardiac devices leads to an increasing amount of device-related workload, e.g. regular in-office follow-ups (FU). New means of ICD FU strategies are necessary to handle the increasing burden. ICD remote monitoring promises a time- and cost efficient alternative to conventional in-office FU strategies. Many studies have already shown benefits on FU burden reduction, on saving of costs and time, and recently on total mortality. The impact of remote ICD FU on Quality of life, anxiety and depression levels and device acceptance is still under discussion. The aim of this trial is to investigate the influence of additional remote ICD surveillance on the primary endpoint health related quality of life (HRQoL), further on levels of anxiety and depression and on device acceptance.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
June 2014
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
LMU Klinikum
Responsible Party
Principal Investigator
Principal Investigator

Johannes Siebermair, MD

Johannes Siebermair, MD

LMU Klinikum

Eligibility Criteria

Inclusion Criteria

  • Patients willing to participate
  • Patients with new-implantation of an ICD or device replacement due to battery depletion between May 2011 and April 2013
  • Sufficient knowledge of the German language
  • Expectancy of life \>1 years at good clinical status
  • Written informed consent

Exclusion Criteria

  • Age \<18 years
  • Subjects not able to give written informed consent
  • Subjects without sufficient German language skills

Outcomes

Primary Outcomes

Influence of ICD remote monitoring on Quality of Life, measured by the EQ5D questionnaire

Time Frame: 12 months

Secondary Outcomes

  • Influence of ICD remote monitoring on device acceptance, measured by the Florida Patient acceptance scale (FPAS)(12 months)
  • Influence of ICD remote monitoring on levels of anxiety and depression, measured by the HADS questionnaire (Hospital Anxiety and Depression scale)(12 months)

Study Sites (2)

Loading locations...

Similar Trials