Basic life support (simulation)
Conditions
Interventions
Group 1: Mixed methods, longitudinal observational design within the framework of a simulation-based assessment.
Data is collected by recording relevant variables (endpoints) relating to basic life su
Sponsors
Klinik für Anästhesiologie und Intensivmedizin
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Participants who have given their consent to participate.
Exclusion criteria
Exclusion criteria: Potential participants who have not consented to participate. Incomplete data records.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality indicators for cardiopulmonary resuscitation (Composite Outcome) o Chest compression rate (1/min) o Chest compression depth (in mm) o Chest recoil (yes/no) The data is collected continuously during a three-day simulation workshop. The parameters are recorded by sensors located in the simulation model (manikin). | — |
Secondary
| Measure | Time frame |
|---|---|
| - Time to first chest compression (in s) - Hands-off time (in s) - Items of the questionnaire The data is collected continuously as part of a three-day simulation workshop. The parameters are collected by sensors located in the simulation model (manikin). The questionnaire is completed by participants before and after the three-day workshop. | — |
Countries
Germany
Contacts
Public ContactJulian Ganter
Klinik für Anästhesiologie und Intensivmedizin
Outcome results
None listed