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Simulation Training as a Tool to Decrease Occupational Stress in ICU Personnel - Article


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Occupational Violence


Clinical Trial: Simulation Training as a Tool to Decrease Occupational Stress in ICU Personnel

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: NCT00232323

Purpose

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.
Condition Intervention
Education, Health
 Behavior: simulation training

MedlinePlus consumer health information 

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

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

Further study details as provided by Sheba Medical Center:
Primary Outcomes: reduction of stress parameters
Expected Total Enrollment:  40

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

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.

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  NCT00232323

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

Israel
      Sheba Medical Center, Tel Hashomer,  Israel
Asaph E 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:  3711/2005
Last Updated:  December 8, 2005
Record first received:  October 2, 2005
ClinicalTrials.gov Identifier:  NCT00232323
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
ClinicalTrials.gov processed this record on 2006-01-10


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October 13, 2008



Page Updated: June 12, 2007
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