Quality of Chest Compressions After a Night Shift

NCT ID: NCT02123810

Last Updated: 2015-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-04-30

Study Completion Date

2014-10-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Cardiac Arrest

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Control

The investigators measure quality of chest compressions before nightshift. Control group

Group Type OTHER

CPR

Intervention Type OTHER

Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes

OFF

The investigators measure quality of chest compressions before nightshift. After night shift group

Group Type OTHER

CPR

Intervention Type OTHER

Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes

Interventions

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CPR

Simulated cardiac arrest on a manikin Chest Compression CPR for 6 minutes

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Resident / Physicians in emergency departement (ED) or taking night in ED
* Resident / Physicians in Intensive Care Unit (ICU) or taking night in ED
* Nightshift \> 18 hours

Exclusion Criteria

* Stop chest compressions before 2 minutes
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Bistro Study Group

OTHER

Sponsor Role lead

Responsible Party

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Yonathan Freund

Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yonathan Freund

Role: PRINCIPAL_INVESTIGATOR

Emergency Department, Hôpital Pitié-Salpêtrière, 47-83 Boulevard de l'Hôpital, 75013 Paris, France.

Locations

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Hôpital Pitié-Salpêtrière; Hopital Saint Antoine; Hopital Tenon

Paris, , France

Site Status

Countries

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France

Other Identifiers

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BG-CAN

Identifier Type: -

Identifier Source: org_study_id

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