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

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

Study Contact Backup

Study Locations

    • Ontario
      • Markham, Ontario, Canada, L3P 7P3
        • Recruiting
        • Markham Stouffville Hospital
        • Contact:
        • 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.

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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