Trottinettes Urgences 2019-2020

Risk Assessment, Consequences and Epidemiology of Electric Scooter Accidents Admitted to Emergency Departments.

The purpose of the study was to evaluate the risk, consequences and epidemiology of electric scooter accidents admitted to the emergency room at St. Pierre University Hospital.

This prospective observational study aims to include any patient admitted to the Adult Emergency Department of St.Pierre University Hospital Brussels following an accident related to the use of an electric scooter in order to describe and understand the epidemiology, complications and treatment of injuries associated with this means of transport.

It is intended to include all accidents occurring in the emergency room during the period from 01/06/2019 to 30/06/2020.

Study Overview

Detailed Description

All patients over the age of 16 years with traumatic injuries due to an accident related to the use of an electric scooter were included in the study.

Upon admission to the Emergency Department, patients over 16 years of age who accepted were included in the study. The objectives of the study were firstly to describe the context and incidence of scooter accidents, and secondly to understand the epidemiology, complications and treatment of injuries associated with this means of transport and finally, to estimate the economic impact assessed by the number of days of post-traumatic work disability, the need for access to more specialised and therefore more expensive care (operating theatre interventions, scanner-type radiological examinations or hospitalisation in intensive care units).

The data analyzed were based on :

1) the time and day of the accident, 2) the time of presentation at the hospital (same day or after the accident), 3) the mechanism of the accident, whether there were one or two people on the scooter, 4) the use or non-use of the protective helmet, 5) the influence of alcohol ; 6) the mode of arrival at the emergency room (type of ambulance or by one's own means); 7) the injury assessment, paraclinical examinations; 8) treatments; 9) hospitalization or not; 10) temporary work interruptions .

Study Type

Observational

Enrollment (Actual)

170

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Bruxelles, Belgium, 1000
        • CHU Saint-Pierre

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

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All the patient presenting at the ED for traumatic lesion following e-sccoter accident

Description

Inclusion criteria:

  • All patients with traumatic lesion following electric sccoter accident
  • Be able to agree to participate in the study

Exclusion Criteria:

  • < 16 years
  • Unconscious
  • Being unable to agree to participate in the study

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
description of traumatic injuries
Time Frame: during the first 24 hours.
description of traumatic injuries based on the medical record. Categorised by severity and by anatomical localisation.
during the first 24 hours.
Arrival mode
Time Frame: Up to one year
By ambulance or by own means
Up to one year
Timing of arrival
Time Frame: Baseline
Immediately after the accident or delayed visit.
Baseline
Accident mechanism
Time Frame: Baseline
Other party ( Pedestrians hit by the scooter, accident with another) involved or not ( Loss of balance,2 drivers on the e-scooter,
Baseline
alcohol
Time Frame: baseline up to 24 hours
Did the driver report to being under the influence of alcohol or not
baseline up to 24 hours
Hour of admission
Time Frame: Baseline up to 24 hours
Admission between 7am-6pm; 6pm-11pm or 11pm-7am
Baseline up to 24 hours
Ownership
Time Frame: Baseline up to 24 hours
E-scooter owned or rented by the patient
Baseline up to 24 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Treatment
Time Frame: Up to 24 hours
Emergency department or operative room
Up to 24 hours
Paraclinical examination
Time Frame: Up to 24 hours
radiography, scanner,
Up to 24 hours
orientation
Time Frame: Up to 24 hours
Intensive care unit, normal hospitalisation, discharge home
Up to 24 hours
Cost of the treatment
Time Frame: Through study completion, an average of 1 year
Ambulance, hospitalisation, treatment in the ED or operative room , temporary incapacity for work.
Through study completion, an average of 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Pierre YOUATOU TOWO, Centre Hospitalier Universitaire Saint Pierre

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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)

June 1, 2019

Primary Completion (Actual)

June 30, 2020

Study Completion (Actual)

March 31, 2021

Study Registration Dates

First Submitted

February 18, 2021

First Submitted That Met QC Criteria

February 26, 2021

First Posted (Actual)

March 3, 2021

Study Record Updates

Last Update Posted (Actual)

April 21, 2022

Last Update Submitted That Met QC Criteria

April 20, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

After publication all IPD will be made available through researchgate.com profile of backup investigator

IPD Sharing Time Frame

After publication

IPD Sharing Access Criteria

Acces will be granted to any researcher requesting access through Researchgate.com

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

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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