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Influence of Telemonitoring on the Management of LVAD-patients

Association of Telemonitoring With Hospitalization Rates and Quality of Life in Patients With End-stage Heart Failure and Implanted Left Ventricular Cardiac Assist Devices

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04613401
Enrollment
50
Registered
2020-11-03
Start date
2020-07-01
Completion date
2021-12-31
Last updated
2020-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Telemedicine, Ventricular Assist Device

Brief summary

The current study aims to investigate whether telemedical monitoring in patients with terminal heart failure and an implanted left ventricular assist device (LVAD) has an influence on LVAD-associated complications, hospitalization rates and quality of life. This is a prospective observational study. Patients with terminal heart failure and an implanted LVAD, where the indication for telemonitoring has already been stated by the attending physician are included in the study. Written informed consent is obtained from all patients. The telemedical monitoring is carried out by the West German Center for Applied Telemedicine (WZAT) and includes a standardized telephone interview every 3 days. In addition, all patients are equipped with an INR measuring device, a body scale and a clinical thermometer by WZAT. The data is documented in an electronic case file (medPower®). In the event of abnormalities, the West German Heart and Vascular Center (WHGZ) is contacted, and all necessary measures are initiated.

Interventions

OTHERquestionnaire (observational study)

questionnaire about hospitalisation rates, complications (bleeding, infection, thrombosis), quality of life (Kansas-Score), depression (PHQ8)

Sponsors

University Hospital, Essen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Age\> 18 years * Indication for telemedicine * Permanently implanted left ventricular assist device (VAD)

Exclusion criteria

* no possibility of telephone contact * patient does not speak german * incompliance * rejection or inability to give consent

Design outcomes

Primary

MeasureTime frameDescription
Number of days spent in the hospital due to VAD-associated complications6 monthsVAD-associated complications are defined as * bleeding with the need for a transfusion * infection with the need for an antibiotic therapy * thrombosis with the need for a lysis therapy

Secondary

MeasureTime frameDescription
Change in quality of life from baseline6 monthsQuality of life will be assessed with the Kansas City Cardiomyopathy Questionnaire (KCCQ) -\> The raw values of the domains are transformed to a scale from 0 to 100, where high values indicate good condition.
Change in depression from baseline6 months\- Depression will be assessed with the Patient Health Questionnaire eight-item depression scale (PHQ-8) -\> The raw values of the domains are transformed to a scale from 0 to 24, where high values indicate a depression.
Number of VAD-associated complications6 monthsVAD-associated complications are defined as * bleeding with the need for a transfusion * infection with the need for an antibiotic therapy * thrombosis with the need for a lysis therapy

Countries

Germany

Contacts

Primary ContactJulia Hoffmann
julia.hoffmann@uk-essen.de+49 201 723 85587

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026