Hôpital Pitié-Salpêtrière; Hopital Saint Antoine; Hopital Tenon
Paris, France
NCT Number: NCT02123810
The investigators sought to evaluate the influence of fatigue after a night shift on the quality of Chest Compressions (CC) in CardioPulmonary Resuscitation (CPR), among physicians.
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Interventional
Not applicable
Paris, France
This is a non inferiority cluster randomized trial on three Emergency Departments (ED) and five Intensive Care Unit (ICU) from three urban academic hospital in Paris, France. The investigators evaluated the quality of CC with a low-fidelity manikin and its electronic feedback device. The investigators tested subjects on a 6-minutes CC-only CPR scenario, including 2 minutes of pause. Physicians were tested either on a control day then after a night shift, or after a night shift then on a control day.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes
Time frame: 2 minutes of chest compressions
The investigators evaluated the quality of CC with a low-fidelity manikin and its electronic feedback device.
Time frame: 2 minutes
The investigators evaluated the quality of CC with a low-fidelity manikin and its electronic feedback device.
Time frame: 2 minutes
The investigators assessed factors associated with better chest compressions as : age, sex and fatigue of physician and intensity of the nightshift.
Bistro Study Group
Other
Weaker Chest Compression After Nightshift : The We CAN Study.
Acronym: WeCAN
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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