I46
Conditions
Interventions
Group 1: Medical laypersons participating in the study receive four different app-linked feedback applications in a predetermined randomised order for use in a resuscitation training setting in the Sk
Sponsors
Uniklinik Köln, Klinik für Anästhesiologie und Operative Intensivmedizin
Eligibility
Sex/Gender
All
Age
18 Years to 49 Years
Inclusion criteria
Inclusion criteria: persons without special previous medical knowledge aged 18-49 years prior written informed consent after written and oral information
Exclusion criteria
Exclusion criteria: Persons not capable of giving consent, pregnant women, breast-feeding mothers, persons who have a medical profession (e.g. paramedic, nurse, doctor) (applicable to subject study 1), persons aged 50 years and older, persons with coronary heart disease, with higher-grade COPD or the presence of another pre-existing condition that would make the performance of cardiopulmonary resuscitation for a duration of 8 minutes seem impossible or with possible risks or possibly associated with health consequences for the subject. Persons with insufficient German language skills.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Achieving guideline-compliant resuscitation quality (compression depth 5-6 cm, compression frequency 100-120/min, correct hand positioning, correct complete relief, no-flow-time, hands-off-time). | — |
Secondary
| Measure | Time frame |
|---|---|
| Influence on self-confidence Assessment of usability | — |
Countries
Germany
Contacts
Public ContactSabine Wingen
Uniklinik Köln, Klinik für Anästhesiologie und Operative Intensivmedizin
Outcome results
None listed