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

Sponsor
Universiteit Antwerpen (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05765045
Collaborator
Heilig Hartziekenhuis, Mol (Other)
220
2
9.9

Study Details

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).

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Nursing triage protocol
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
220 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Intervention group and control groupIntervention group and control group
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
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
Anticipated Study Start Date :
Mar 6, 2023
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Nursing triage group

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

Diagnostic Test: Nursing triage protocol
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.

No Intervention: Regular care group

Regular triage in the emergency department

Outcome Measures

Primary Outcome Measures

  1. TLOS [6-8 weeks]

    Total length of stay

Secondary Outcome Measures

  1. Patient satisfaction [6-8 weeks]

    Patient satisfaction measured by a 10-point Likert scale at discharge using a questionnaire

  2. Treatment efficiency [6-8 weeks]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universiteit Antwerpen
  • Heilig Hartziekenhuis, Mol

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Filip Haegdorens, Principal Investigator, Universiteit Antwerpen
ClinicalTrials.gov Identifier:
NCT05765045
Other Study ID Numbers:
  • TRINU-RX
First Posted:
Mar 13, 2023
Last Update Posted:
Mar 13, 2023
Last Verified:
Feb 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 13, 2023