NCT00232323

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.

Trial Health

33
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Trial recruitment is currently suspended
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2006

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
suspended

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 2, 2005

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 4, 2005

Completed
3 months until next milestone

Study Start

First participant enrolled

January 1, 2006

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2006

Completed
Last Updated

January 24, 2007

Status Verified

January 1, 2007

First QC Date

October 2, 2005

Last Update Submit

January 23, 2007

Conditions

Keywords

intensive carestresseducationsimulation

Outcome Measures

Primary Outcomes (1)

  • reduction of stress parameters

Interventions

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • unwilling to participate

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sheba Medical Center

Tel Litwinsky, Israel

Location

MeSH Terms

Conditions

Health Education

Condition Hierarchy (Ancestors)

Adherence InterventionsMedication AdherencePatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Asaph E Nini, MD

    Sheba Medical Center and Medical Simulation Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
ECT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

October 2, 2005

First Posted

October 4, 2005

Study Start

January 1, 2006

Study Completion

June 1, 2006

Last Updated

January 24, 2007

Record last verified: 2007-01

Locations