Trauma Triage Decision With Software (TraumaDS)

Sponsor
Derince Training and Research Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03357835
Collaborator
(none)
1,000
1
4.9
204.3

Study Details

Study Description

Brief Summary

It is intended to show that a computer software called Trauma Decision System (TravmaDS) for the determination of the urgency of trauma patients who applied to Emergency Medical Clinic gives more accurate, more objective, faster results than the triage scored by medical and non-medical personnel and to show the fact that TraumaDS provides more patient satisfaction.

Condition or Disease Intervention/Treatment Phase
  • Other: Trauma Decision System

Detailed Description

There are limitations in our routine standard of practice in Emergency medical clinic in rapid triage about the adequacy particularly in the patient group where specific and rapid decision-making, such as trauma. The process of evaluating the patients who are directed to the green area unnecessarily in trauma care by the physician is prolonged, the evaluation process of patients who are directed to the red area unnecessarily shortens but hospital resources are being used extensively. Therefore, in this study, it was planned to perform objective triage with a computer based scoring system. Triage scoring determined by the Ministry of Health (SB ), routinely performed by an emergency medical technician (EMT), will be applied when the patients are admitted to emergency services. According to this scoring, patients who need urgent care and who should not wait less than 15 minutes will be considered red coded, patients who can wait up to 60 minutes will be considered yellow coded, patients who can wait for 120 minutes or more will be considered green coded. To the other group, triage maintenance / evaluation will be done with computer software developed by us. All patients with trauma should be included in the study, demographic data, trauma mechanism and trauma type vital signs at the time of application of the patients will be routinely observed in both groups of patients. These observations are routine for this disease group and we will not undertake any interventional procedures or screening except special routine application for research purposes. The observation and file information will be organized by the triage staff in both groups at the time of the application of the patients. In this software-based program before working on the software informative training will be given to triage staff and for this patient triage handheld computers will be given to triage staff. In order for the referring patients to be able to see the entries made with the triage software a simultaneous large-screen monitor will be used. At the time of application, color codes indicating the urgency of the patients will be given according to the demographic data of the patients, the type of trauma and the vital signs were directed by the software program. As a result of the software program's direction, patients will be coded as green-yellow-orange-red area and patient care will be made in accordance with these codes.

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Triage With Software Assistance To Trauma Patient Who Attending To Emergency Department
Actual Study Start Date :
Nov 1, 2017
Anticipated Primary Completion Date :
Jan 31, 2018
Anticipated Study Completion Date :
Mar 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Normal Triage

Triage scoring determined by the Ministry of Health (SB ), routinely performed by an emergency medical technician (att), will be applied when the patients are admitted to emergency services. According to this scoring, patients who need urgent care and who should not wait less than 15 minutes will be considered red coded, patients who can wait up to 60 minutes will be considered yellow coded, patients who can wait for 120 minutes or more will be considered green coded.

Software Triage

triage maintenance / evaluation will be done with computer software called "Trauma Decision System (TraumaDS)" developed by us. As a result of the software program's direction, patients will be coded as green-yellow-orange-red area and patient care will be made in accordance with these codes. According to this scoring, patients who need urgent care and who should not wait will be considered red code, patients who should wait less than 15 minutes will be considered orange coded, patients who can wait up to 60 minutes will be considered yellow coded, patients who can wait for 120 minutes or more will be considered green coded.

Other: Trauma Decision System
At the time of application, color codes indicating the urgency of the patients will be given according to the demographic data of the patients, the type of trauma and the vital signs were directed by the software program. As a result of the software program's direction, patients will be coded as green-yellow-orange-red area and patient care will be made in accordance with these codes.

Outcome Measures

Primary Outcome Measures

  1. Difference between software triage time and traditional triage time [5 minutes]

    Investigation difference of triages made by software and normal triage

Secondary Outcome Measures

  1. 30-day mortality [30 days]

    Defined as mortality within 30 days of arrival to hospital

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • all trauma patients who want to participate
Exclusion Criteria:
  • who do not want to participate, who are not triaged, who leave the hospital before the treatment is completed

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kocaeli Derince Training and Research Hospital Derince Kocaeli Turkey 41900

Sponsors and Collaborators

  • Derince Training and Research Hospital

Investigators

  • Principal Investigator: Ahmet Akdoğan, RA, Research Assistant

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmet Akdoğan, Emergency Medicine Research Assistant, Derince Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT03357835
Other Study ID Numbers:
  • 2017/145
First Posted:
Nov 30, 2017
Last Update Posted:
Nov 30, 2017
Last Verified:
Nov 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Ahmet Akdoğan, Emergency Medicine Research Assistant, Derince Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 30, 2017