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 memory decay, Scenario B includes a 3-minute delay before completing the questionnaire, matching the interval between information exposure and recall in Scenario A.
After each scenario, participants complete the NASA-TLX workload assessment and a semi-open questionnaire on the patient's history. A modified Brown-Peterson task follows as a washout period: participants subtract 3 repeatedly from 309 for 1 minute, followed by 4 minutes of rest without phone use or conversation. Calculation performance is not analyzed.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
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.
Disqualifiers
None
Trial design
Crossover
Treatments tested in this trial
Recall of History
BehavioralRecall of history heard during or without performing CPR
CPR
Procedure/SurgeryPerforming CPR in a 30:2 manner
Treatment groups
Trial outcomes
Primary outcomes
History items
Number of correct items
Secondary outcomes
NASA-TLX
Nasa Task load index (min: 0, max: 120, higher scores mean higher cognitive load)
Sponsors and contacts
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