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A Nursing Triage Protocol for Minor Orthopedic Traumata: the Effect on Flow Time, Quality of Care and Patient Satisfaction in an Emergency Department (TRINU-RX)

Primary Purpose

Trauma Injury

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Nursing triage protocol
Sponsored by
Universiteit Antwerpen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Trauma Injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Adults (18 years old) ESI 4 or ESI 5 Recent trauma (< 10 days after trauma) Accidental trauma mechanism Trauma below the elbow (forearm, wrist, hand, finger) Trauma below the knee (lower leg, ankle, foot, toe) Exclusion Criteria: ESI 1 or ESI 2 or ESI 3 Return visit after previous emergency department contact for the same injury (e.g. increased pain, tight cast, ...) Trauma resulting from underlying somatic pathology (e.g. syncope, epileptic attack, vertigo, vasovagal collapse, ...) Atraumatic (pain) complaints (e.g. pain in the calf, toe, foot, wrist, ... without a clear trauma mechanism) Additional, non-orthopedic injuries (e.g. laceration, signs of cerebral commotion, ...) Pregnancy or a suspicion of pregnancy

Sites / Locations

  • University of Antwerp

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Nursing triage group

Regular care group

Arm Description

Using a triage protocol for medical imaging conducted by a triage nurse in the emergency department

Regular triage in the emergency department

Outcomes

Primary Outcome Measures

TLOS
Total length of stay

Secondary Outcome Measures

Patient satisfaction
Patient satisfaction measured by a 10-point Likert scale at discharge using a questionnaire
Treatment efficiency
Measurement if the patient diagnosis and/or treatment was correctly initiated at the Emergency Department. Yes = no additional diagnosis or treatments were necessary; No = within 14 days after discharge a change in treatment or new diagnosis was done. Data will be collected using the hospital's patient records or by calling patients if no information is found in the record.

Full Information

First Posted
February 9, 2023
Last Updated
June 28, 2023
Sponsor
Universiteit Antwerpen
Collaborators
Heilig Hartziekenhuis, Mol
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1. Study Identification

Unique Protocol Identification Number
NCT05765045
Brief Title
A Nursing Triage Protocol for Minor Orthopedic Traumata: the Effect on Flow Time, Quality of Care and Patient Satisfaction in an Emergency Department
Acronym
TRINU-RX
Official Title
A Nursing Triage Protocol for Minor Orthopedic Traumata: the Effect on Flow Time, Quality of Care and Patient Satisfaction in an Emergency Department
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
March 6, 2023 (Actual)
Primary Completion Date
April 23, 2023 (Actual)
Study Completion Date
April 23, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiteit Antwerpen
Collaborators
Heilig Hartziekenhuis, Mol

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In 2019, nearly half of all hospital contacts in Belgium took place through the emergency department, and more than a third of patients arrived after an accident or trauma. In instances of overcrowding, patients with minor orthopedic injuries face prolonged waiting times. Previous studies have shown that implementing triage protocols for medical imaging conducted by a triage nurse can reduce the Total Length of Stay (TLOS) for this patient group. This is a single-center, unblinded, randomized, controlled trial that aims to evaluate the impact of a nurse triage protocol on turnaround time (primary outcome), quality of care, and patient satisfaction. The study population consists of adults who present with minor orthopedic injuries below the elbow or knee and have an Emergency Severity Index (ESI) of 4 or 5. Participants are randomly assigned to either the 'nurse triage protocol' group (n=110) or the 'usual care' group (n=110).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trauma Injury

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Intervention group and control group
Masking
None (Open Label)
Allocation
Randomized
Enrollment
220 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nursing triage group
Arm Type
Experimental
Arm Description
Using a triage protocol for medical imaging conducted by a triage nurse in the emergency department
Arm Title
Regular care group
Arm Type
No Intervention
Arm Description
Regular triage in the emergency department
Intervention Type
Diagnostic Test
Intervention Name(s)
Nursing triage protocol
Intervention Description
Medically approved and supervised standing order that allows trained ER nurses to start medical imaging (RX) for adult patients with minor traumata to the limbs.
Primary Outcome Measure Information:
Title
TLOS
Description
Total length of stay
Time Frame
6-8 weeks
Secondary Outcome Measure Information:
Title
Patient satisfaction
Description
Patient satisfaction measured by a 10-point Likert scale at discharge using a questionnaire
Time Frame
6-8 weeks
Title
Treatment efficiency
Description
Measurement if the patient diagnosis and/or treatment was correctly initiated at the Emergency Department. Yes = no additional diagnosis or treatments were necessary; No = within 14 days after discharge a change in treatment or new diagnosis was done. Data will be collected using the hospital's patient records or by calling patients if no information is found in the record.
Time Frame
6-8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adults (18 years old) ESI 4 or ESI 5 Recent trauma (< 10 days after trauma) Accidental trauma mechanism Trauma below the elbow (forearm, wrist, hand, finger) Trauma below the knee (lower leg, ankle, foot, toe) Exclusion Criteria: ESI 1 or ESI 2 or ESI 3 Return visit after previous emergency department contact for the same injury (e.g. increased pain, tight cast, ...) Trauma resulting from underlying somatic pathology (e.g. syncope, epileptic attack, vertigo, vasovagal collapse, ...) Atraumatic (pain) complaints (e.g. pain in the calf, toe, foot, wrist, ... without a clear trauma mechanism) Additional, non-orthopedic injuries (e.g. laceration, signs of cerebral commotion, ...) Pregnancy or a suspicion of pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Filip Haegdorens, PhD
Organizational Affiliation
University of Antwerp, Belgium
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Antwerp
City
Wilrijk
State/Province
Antwerp
ZIP/Postal Code
2610
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Nursing Triage Protocol for Minor Orthopedic Traumata: the Effect on Flow Time, Quality of Care and Patient Satisfaction in an Emergency Department

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