- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05937763
ED Adaptive Staffing Study (FAST-ED)
March 20, 2024 updated by: Oak Valley Health
Feasibility and Evaluation of an Adaptive STaffing Model in a Community Emergency Department (FAST-ED)
Emergency Departments (EDs) across Ontario are being inundated with unprecedented high patient volumes and a staffing shortage that directly impacts patient care and flow.
An area of concern among EDs is the offload zone where patients are brought in by ambulance.
EMS offload time is the time it takes paramedics to transfer a patient to the appropriate area within an emergency department and give hospital staff a summary of what concerns the patient is seeking care for.
There are multiple factors that may delay this time, including limited staff in the offload area to complete the transfer process due to competing patient care responsibilities.
The adaptive staffing model study will look to add a primary care paramedic (PCP) or a registered nurse (RN) in the offload zone during times of high ambulance volume (August to January) to help with patient care within the offload zone.
This single-centered community hospital study will evaluate the benefits of having a PCP or RN, compared to the current model, on ambulance offload times, patient safety outcomes, patient treatment times, and staff well-being using three different models of staffing.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
5917
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Andrew Arcand, MD
- Phone Number: 905-472-7373
- Email: AArcand@oakvalleyhealth.ca
Study Contact Backup
- Name: Michelle Dimas, MSc
- Phone Number: 6253 905-472-7373
- Email: mdimas@oakvalleyhealth.ca
Study Locations
-
-
Ontario
-
Markham, Ontario, Canada, L3P 7P3
- Recruiting
- Markham Stouffville Hospital
-
Contact:
- Michelle Dimas, MSc
- Phone Number: 6253 9054727373
- Email: mdimas@oakvalleyhealth.ca
-
Principal Investigator:
- Andrew Arcand, MD
-
Principal Investigator:
- Philip Moran, MD
-
Sub-Investigator:
- Michelle Dimas, MSc
-
Sub-Investigator:
- Jinal Patel, RN
-
Sub-Investigator:
- Ainslee Smith, RN
-
Sub-Investigator:
- Carissa Surujpaul, RN
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study will use a convenience sampling method, given that patients brought in by ambulance are at random and non-predictive.
Description
Inclusion Criteria:
- Patients brought in by ambulance to hospitals emergency department offload area
Exclusion Criteria:
- Patients not arriving to the hospitals emergency department offload area
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Primary Care Paramedic (PCP) Block
A PCP will be staffed in the emergency department offload zone 3 days a week (Monday, Wednesday, and Friday) on a 10am - 10pm shift, in addition to the standard staffing model.
|
Staffing the hospitals emergency department offload zone with a PCP or RN or current workflow.
|
Registered Nurse (RN) Block
An experienced emergency department RN with triage training will be staffed in the emergency department offload zone 3 days a week (Monday, Wednesday, and Friday) in a 10am - 10pm shift, in addition to the standard staffing model
|
Staffing the hospitals emergency department offload zone with a PCP or RN or current workflow.
|
Current Workflow Block
The currently hospitals staffing models of the emergency department offload zone.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Triage Time
Time Frame: 6 months
|
The aim of this objective is to compare time to triage and time to transfer of care for three models of staffing.
|
6 months
|
Return to Service
Time Frame: 6 months
|
The aim of this objective is to determine if an adaptive staffing model during peak volumes reduces ambulance offload times and return to service.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Time to provider assessment
Time Frame: 6 months
|
6 months
|
|
Provider Feedback Survey
Time Frame: 6 months
|
Explore provider perceptions (ED staff and paramedics) of each model with the aim of determining which model provides better patient care during peak volumes.
Participants will self-report their perceived barriers, challenges and benefits of the staffing interventions.
|
6 months
|
Time to treatment
Time Frame: 6 months
|
6 months
|
|
Time to disposition
Time Frame: 6 months
|
6 months
|
|
Number of incident reports
Time Frame: 6 months
|
Patient safety events
|
6 months
|
Case costing
Time Frame: 6 months
|
6 months
|
|
Well-being Index (questionnaire)
Time Frame: 6 months
|
Explore staff and paramedic well-being on intervention model
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 2, 2023
Primary Completion (Estimated)
March 1, 2024
Study Completion (Estimated)
September 1, 2024
Study Registration Dates
First Submitted
June 23, 2023
First Submitted That Met QC Criteria
June 30, 2023
First Posted (Actual)
July 10, 2023
Study Record Updates
Last Update Posted (Actual)
March 22, 2024
Last Update Submitted That Met QC Criteria
March 20, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 148-2306
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Aggregate data and study results will be shared via publication and conference presentations.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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