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Clinical Decision Unit (CDU) - Evaluation of a Novel Approach to Address Emergency Department Overcrowding

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ClinicalTrials.gov Identifier: NCT00497393
Recruitment Status : Completed
First Posted : July 6, 2007
Last Update Posted : September 12, 2008
Sponsor:
Collaborator:
Information provided by:

Study Description
Brief Summary:
This randomized controlled trial will introduce a Clinical Decision Unit (CDU) into the University of Alberta Hospital Emergency Department(ED)and assess the influence on ED length of stay, patients who leave without being seen, and other ED Overcrowding outcomes.

Condition or disease Intervention/treatment Phase
Acute Illness Behavioral: Clinical Decision Unit Phase 4

Detailed Description:
The study will take place over a 6-week period that will be spilt into three-two-week blocks. Using computerized blocks of 2 weeks, days of the week will be randomly allocated so that each day of the week receives one intervention (CDU) and one control day for the study period. The CDU involves transforming an ED bed location to a 6-chair internal waiting room with 2 adjacent beds assigned to act as assessment and treatment locations. Patients will transition between the chair and stretcher to optimize the use of ED space.

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 6217 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: Clinical Decision Unit (CDU) - Evaluation of a Novel Approach to Address Emergency Department Overcrowding
Study Start Date : July 2007
Primary Completion Date : August 2007
Study Completion Date : December 2007
Arms and Interventions

Arm Intervention/treatment
No Intervention: Control
regular use of the 2-bed areas in the Emergency department
Behavioral: Clinical Decision Unit
a dedicated 2-bed area to see patients and then rotate them back into the waiting room area for labs and diagnostic imaging.


Outcome Measures

Primary Outcome Measures :
  1. Total ED length of stay [ Time Frame: in the Emergency Department ]

Secondary Outcome Measures :
  1. Left without being seen (LWBS) rates [ Time Frame: in the Emergency Department ]
  2. nurse and physician satisfaction [ Time Frame: following Emergency Department shift ]
  3. ambulance turnaround times (time [ Time Frame: in the Emergency Department ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   17 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Only adult patients (>17 years of age) presenting to the University of Alberta Hospital Emergency Department (UAH ED), during the study interval will be included in the evaluation.

Exclusion Criteria:

  • Direct admits/Pediatric patients.
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00497393


Locations
Canada, Alberta
University of Alberta Hospital
Edmonton, Alberta, Canada, T6G 2B7
Sponsors and Collaborators
University of Alberta
Capital Health, Canada
Investigators
Principal Investigator: Michael Bullard, MD University of Alberta Hospital, Edmonton, Alberta, T6G 2B7, Canada
More Information

Responsible Party: Brian Holroyd, University of Alberta
ClinicalTrials.gov Identifier: NCT00497393     History of Changes
Other Study ID Numbers: B-130607
First Posted: July 6, 2007    Key Record Dates
Last Update Posted: September 12, 2008
Last Verified: September 2008

Keywords provided by University of Alberta:
Emergency department, administration, overcrowding

Additional relevant MeSH terms:
Emergencies
Disease Attributes
Pathologic Processes