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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00991471
Other study ID # 226-2009
Secondary ID
Status Completed
Phase N/A
First received October 5, 2009
Last updated October 27, 2017
Start date September 2009
Est. completion date February 2010

Study information

Verified date October 2017
Source Sunnybrook Health Sciences Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to investigate whether the introduction of a physician-nurse supplementary triage assessment team (MDRN STAT) is effective in improving time-based performance indicators for wait times. Secondary objectives will examine the quality of patient care and health care worker satisfaction and the cost-effectiveness of the program


Description:

In 2007, the Ontario Ministry of Health and Long-term Care (MOHLTC) declared emergency department wait-times a government priority. The crisis of overcrowding and access block has become an international epidemic, affecting developing countries in Europe, North America, and Australasia. The MOHLTC has targeted 23 Ontario hospitals' prolonged wait times. Sunnybrook Health Sciences Center has been selected. Therefore, this is a quality improvement study of patient wait-times and care.

During a 20-week period, the MDRN STAT will be present on randomly chosen weekdays (8:00-16:00) for 50 shifts. Wait-times, such as time from triage time to: physician assessment, stretcher occupation, treatment orders (drugs), investigation orders (laboratory, diagnostic imaging), investigation acquisition (diagnostic imaging), consultation, bed request, discharge from ED (i.e. length of stay (LOS)) time, will be analyzed. In addition, the left-without-being-seen rate (LWBS) and rate of return will be analyzed. These results will be compared to the Ontario wait-time strategy P4R targets, as well as the Canadian Triage Acuity Scale (CTAS guidelines). Economic analysis of this intervention will be done. The hospital will independently perform patient satisfaction surveys. Health care worker satisfaction survey data will be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 6300
Est. completion date February 2010
Est. primary completion date February 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients arriving from 8:00-14:30 during a day here a MDRN STAT is assigned

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Interaction with MDRN STAT
Interaction with MDRNSTAT at triage to obtain orders for investigations and/or treatment
No MDRNSTAT
Standard management of nurse-only triage for assignment of CTAS

Locations

Country Name City State
Canada Sunnybrook Health Sciences Center Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Effectiveness of the MDRN STAT on emergency department wait times Time from triage to time of discharge from ED
Secondary Cost-Effectiveness of a MDRN STAT in the Emergency Department 6 months, of 50 MDRN STAT shifts, randomized with non-intervention
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