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

This study has suspended participant recruitment.
Sponsor:
Information provided by:
Sheba Medical Center
ClinicalTrials.gov Identifier:
NCT00232323
First received: October 2, 2005
Last updated: January 23, 2007
Last verified: January 2007
  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
Behavioral: simulation training

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Educational/Counseling/Training
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 Outcome Measures:
  • reduction of stress parameters

Estimated Enrollment: 40
Study Start Date: January 2006
Estimated Study Completion Date: June 2006
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.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • unwilling to participate
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00232323

Locations
Israel
Sheba Medical Center
Tel Hashomer, Israel
Sponsors and Collaborators
Sheba Medical Center
Investigators
Principal Investigator: Asaph E Nini, MD Sheba Medical Center and Medical Simulation Center
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00232323     History of Changes
Other Study ID Numbers: SHEBA-05-3711-AN-CTIL
Study First Received: October 2, 2005
Last Updated: January 23, 2007
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Sheba Medical Center:
intensive care
stress
education
simulation

ClinicalTrials.gov processed this record on October 23, 2014