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Simulation Training as a Tool for Teamwork Improvement in Multidisciplinary Intensive Care Team - Article


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Clinical Trial: Simulation Training as a Tool for Teamwork Improvement in Multidisciplinary Intensive Care Team

This study is not yet open for patient recruitment.
Verified by Sheba Medical Center October 2005

Sponsored by: Sheba Medical Center
Information provided by: Sheba Medical Center
ClinicalTrials.gov Identifier: NCT00229411

Purpose

The purpose of the study is to check whether training mixed teams of physicians and nurses from intensive care units on patient simulators improves teamwork within the teams.
Condition Intervention
Education, Health
 Behavior: simulation training

MedlinePlus consumer health information 

Study Type: Interventional
Study Design: Educational/Counseling/Training, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Efficacy Study

Official Title: Experimental Like Observational Study of Teamwork Improvement in Multidisciplinary Intensive Care Team Before and After Simulation Training.

Further study details as provided by Sheba Medical Center:
Primary Outcomes: improvement in teamwork parameters as measured by previously published tools
Expected Total Enrollment:  40

Study start: January 2006;  Expected completion: December 2006
Last follow-up: May 2006;  Data entry closure: September 2006

Patient safety and the prevention of medical error are primary goals of healthcare organizations. One of the means of reducing such errors is teamwork improvement. Simulation training, using advanced patient simulators, has been shown to improve diagnostic, resuscitation and technical skills amongst physicians and nurses. We intend to compare simulation training of a mixed team of physicians and nurses, using specifically designed scenarios based on real life experience, to frontal teaching sessions designed to enhance teamwork, by assessing teamwork, using accepted behavioral scales, during routine work, before and after both interventions.

Eligibility

Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • unwilling to participate

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00229411

Asaph E Nini, MD      972-3-5302026    asaph.nini@sheba.health.gov.il

Israel
      Sheba Medical Center, Tel Hashomer,  52621,  Israel
Asaph Nini, MD  972-3-5302026    asaph.nini@sheba.health.gov.il 
asaph e nini, MD,  Principal Investigator

Study chairs or principal investigators

Asaph E Nini, MD,  Principal Investigator,  Sheba Medical Center and Medical Simulation Center   

More Information

Study ID Numbers:  3710/2005
Last Updated:  December 8, 2005
Record first received:  September 26, 2005
ClinicalTrials.gov Identifier:  NCT00229411
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2006-01-10


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November 25, 2009



Page Updated: January 17, 2009
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