I48.9
Conditions
Interventions
Group 1: Individuals (n=500) who have independently and voluntarily registered to participate in a marathon will be included in the study. The baseline visit will take place within three days before t
Sponsors
Deutsches Herzzentrum der Charité
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: None
Exclusion criteria
Exclusion criteria: Allergy to medical adhesives Coronary heart disease, history of heart attack or surgical coronary revascularization (bypass surgery) Cardiomyopathy History of cardiac arrhythmias or current use of antiarrhythmic drugs Subjects with (severe) heart valve defects Subjects after reconstructive surgery (Tetralogy of Fallot, AVSD, hemodynamically relevant defects, etc.)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of atrial fibrillation | — |
Secondary
| Measure | Time frame |
|---|---|
| Occurrence of other different heart rhythm disorders | — |
Countries
Germany
Contacts
Public ContactFlorian Blaschke
Deutsches Herzzentrum der Charité
Outcome results
None listed