Optimizing Quality of Life by Improved Patient Expectation Following Atrial Fibrillation Catheter Ablation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorEvangelical Hospital Düsseldorf

About this trial

The aim is to investigate whether optimizing patients' expectations towards the interventional treatment of atrial fibrillation (catheter ablation) leads to a lower disease-related impairment of the patients compared to the control group in the first three months after ablation (the so-called blanking period).

Eligibility criteria

Qualifiers

symptomatic atrial fibrillation

indication for pulmonary vein isolation

sufficient command of the German language

Disqualifiers

age <18 years

permanent atrial fibrillation

presence of psychiatric disorders which impair the study participitatin

presence of another medical condiction which influences quality of life stronger than the cardiac condition

Trial design

Treatments tested in this trial

  • Expectation optimization

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Evangelical Hospital Düsseldorf

Lead sponsor

University Hospital, Essen

Collaborator