A observational study of staff movements and satisfaction with changes to intensive care unit room configuratio

Not Applicable

• Conditions: Optimal intensive care unit room size; Other - Conditions of unknown or disputed aetiology (such as chronic fatigue syndrome/myalgic encephalomyelitis)

• Registration Number: ACTRN12607000574448
• Lead Sponsor: Intensive Care Unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2007-11-07
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

All nursing staff from Concord Repatriation General Hospital Intensive Care Unit

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Map of staff movements during an 8 hour shift[During staff shift];Staff satisfaction with room configuration accessed using a questionnaire[At end of staff shift]

Secondary Outcome Measures

Name	Time	Method
o secondary outcome[No secondary timepoint]