MultiCPR: The Influence of Resuscitation on History Recall
Recruiting
N/A
Interventional Study
Multitasking Behavior
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 38 (estimated)
- Sponsor
- Medical University of Vienna · Other
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About This Trial
In this randomized crossover trial, participants begin with chest compressions at a 30:2 ratio while a study team member provides ventilation. In Scenario A, participants perform two-person CPR and receive a prerecorded patient history after 30 seconds. In Scenario B, participants only listen to the patient's history without performing CPR or any concurrent task. To control for time-dependent memo…
Trial Locations
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Eligibility Criteria
Inclusion:
* Healthy medical professionals trained in CPR (paramedics, prehospital emergency physicians, anesthesiologists, internal medicine doctors, nurses, midwifery students, pediatricians)
* CPR Training in the last four years
* Fit and rested.
Exclusion:
\- Pregnant probands
Contacts