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Clinical Trials/NCT00232323
NCT00232323SuspendedNot Applicable

Experimental Like Study of Stress Reduction in Intensive Care Teams by Use of Simulation Training

Sheba Medical Center2 sites in 1 country40 target enrollmentStarted: January 2006Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Suspended
Enrollment
40
Locations
2
Primary Endpoint
reduction of stress parameters
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The purpose of the study is to check wether training mixed teams of physicians and nurses from intensive care units on patient simulators reduces stress in team members.

Detailed Description

Patient safety and the prevention of medical error are primary goals of healthcare organizations. Stress reduction may reduce or ameliorate such errors. Simulation training, using advanced patient simulators, has been shown to improve diagnostic, resuscitation and technical skills amongst physicians and nurses.We intend to check wether stress during ICU shifts may be reduced by using specifically designed scenarios based on real life experience,in integrative multidisciplinary ICU teams.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Ect
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •intensive care physicians and nurses working in respiratory ICU willing to participate in the study

Exclusion Criteria

  • •unwilling to participate

Outcomes

Primary Outcomes

reduction of stress parameters

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov

Study Sites (2)

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