- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02703701
Role of Provider-at-Triage on ED Efficiency and Quality of Care (MD at Triage)
Effects of Provider-at-Triage on Emergency Department Efficiency, Information Delivery and Patient Satisfaction
The United States spends over $8,000 per capita annually on health care and its health care system is more expensive than other developed countries. Even with high per capita costs and a high proportion of physician specialists, the US lags in health care performance from patients' perspectives.
The hospital emergency department (ED) is often the portal of entry for patients seeking health care services and is therefore an ideal setting for initiatives to improve efficiency of care delivery and patient satisfaction. Reduction in wait times, enhanced information delivery and ED staff service quality all have a positive influence on patient perception of health care quality and satisfaction.
Prior studies have attempted to increase patient satisfaction by improving staff communication and courtesy, implementing a patient satisfaction team in triage, and delivering information to patients in a timely manner. Another strategy to increase the efficiency of ED operations is adding a physician to triage to perform brief medical screenings and initiate necessary patient testing and treatment. This contrasts to usual practice in which physicians evaluate patients only following registration and nurse assessment of illness or injury severity.
Study Overview
Status
Intervention / Treatment
Detailed Description
This study will assess the impact of early patient assessment by a physician at Emergency Department (ED) triage on patient perception of information delivery, overall patient satisfaction and ED efficiency. ED efficiency will be assessed by ED length of patient stay, ED left-without-being-seen and ED left during treatment rates.
Participants who decide to take part in this study, will be asked questions by research staff, who will document responses on a secure iPAD device. The survey will ask participants how they feel about their health condition, the emergency department wait, the care they received in the emergency department and how satisfied the participant was with the care received.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Florida
-
Gainesville, Florida, United States, 32608
- UF Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Participants are eligible to participate in the study if they are:
- English speaking
- Without hemodynamic or respiratory compromise
- Do not have a nurse-assigned triage severity score of Emergency Severity Index 1 (most severe illness or injury score).
Exclusion Criteria:
Participants will be excluded if they are:
- Unwilling or unable to sign an informed consent
- In police custody
- Too ill to participate in study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Usual Care
Group enrolled during normal emergency department operating procedures (without a physician present at triage).
|
No physician at triage
|
|
Physician at Triage
Group enrolled while a physician is present at triage.
|
A physician embedded at triage
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient Satisfaction
Time Frame: 60 minutes after Emergency Department triage
|
Patient Satisfaction Score- brief survey measured on a Likert Scale
|
60 minutes after Emergency Department triage
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Emergency Department efficiency
Time Frame: 24 hours after ED triage in minutes
|
Impact of physician at triage on ED length of stay rates
|
24 hours after ED triage in minutes
|
|
Left without being seen rate
Time Frame: 12 hours after ED triage in minutes
|
Impact of physician at triage on left without being seen rate
|
12 hours after ED triage in minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brandon Allen, MD, Univeristy of Florida
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB201500586
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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