Evaluation of the quality, usability, and evidence-based assessment of app-connected feedback devices for a resuscitation setting.
Not Applicable
- Conditions
- I46Cardiac arrest
- Registration Number
- DRKS00031876
- Lead Sponsor
- niklinik Köln, Klinik für Anästhesiologie und Operative Intensivmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 47
Inclusion Criteria
persons without special previous medical knowledge
aged 18-49 years
prior written informed consent after written and oral information
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.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method Influence on self-confidence<br>Assessment of usability