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Clinical Trials/NCT03375073
NCT03375073
Completed
Not Applicable

Positive Communication Within Healthcare Team and Clinical Performance: a Prospective, Randomised and Controlled Simulation Trial.

University Grenoble Alps1 site in 1 country32 target enrollmentNovember 29, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Positive Communication
Sponsor
University Grenoble Alps
Enrollment
32
Locations
1
Primary Endpoint
Clinical performance of the anaesthetic team
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The emotional and cognitive impact of positive communication between caregivers remains uninvestigated. The investigators hypothesize that positive communication during medical transmission can increase clinical performance for managing a subsequent stressful unexpected adverse event.

Detailed Description

When caregivers deal with acute stressful adverse events, cognitive overload and negative emotions can impair cognitive abilities and decrease clinical performance. The beneficial effect of positive communication on patients' emotions has widely been studied. However, the emotional and cognitive impact of positive communication between caregivers remains uninvestigated. The primary purpose of this trial is to study the impact of positive communication between anaesthetic teams during medical transmissions on clinical performance for managing a subsequent stressful unexpected adverse event. Secondary outcomes are to study the impact of positive communication on physiological (heart rate variability) and psychological (psychometric scales) levels of stress.

Registry
clinicaltrials.gov
Start Date
November 29, 2017
End Date
September 29, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Grenoble Alps
Responsible Party
Principal Investigator
Principal Investigator

Pierre ALBALADEJO

Clinical Professor, Anesthesiology and Intensive Care

University Grenoble Alps

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Clinical performance of the anaesthetic team

Time Frame: Each anaesthetic team will be involved once in the scenario. The scenario will last about 6 min (transmission not included). Both assessment of clinical performance will be made within 20 weeks of each simulation session

Clinical performance in a simulated scenario of laryngospasm occurring in a 7 year old child under general anaesthesia. Clinical performance will be scored from 0 to 100 by two independent blinded assessors, using video records and a pre-established scenario-specific checklist. The primary endpoint will be the mean of the two assessments for each performance.

Secondary Outcomes

  • Self-reported stress(Before the scenario (at 5 min), after medical transmission (at 7 min), after the scenario (at 13 min), after debriefing (at 33 min))
  • Heart rate variability(Before the scenario (during 5 min), during medical transmission (2 min), during the scenario before the laryngospasm (2 min), during the laryngospasm (4 min), during the debriefing (20 min), after the debriefing (5 min))

Study Sites (1)

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