Impact of a Mediator for Patient Intake in Emergency Departments (MEDIA)

December 12, 2019 updated by: Hospices Civils de Lyon

Welcoming Patients in Emergency Departments: Impact of the Mediator

Violence in the workplace is becoming a serious phenomenon in the contemporary world of work. Hospital staff, like any employee working in contact with the public, is particularly exposed to this violence. In emergency departments, the number of patients treated and their heterogeneity, the problems of communicating with healthcare professionals, and waiting times, favor conflict situations. In the already tense context of the emergencies, the incivilities or violent acts have an impact on the well-being of professionals. In order to prevent these situations of violence, a solution could be to integrate a professional with specific skills into the teams to perform mediation functions between caregivers and patients.

The aim of the study is to evaluate the impact of the presence of a mediator in emergency services on personal (verbal or physical) attacks on professionals (caregivers, doctors, administrative staff).

Study Overview

Study Type

Observational

Enrollment (Actual)

2378

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

      • Lyon, France, 69003
        • Pôle Information Médicale, Evaluation, Recherche - Hospices Civils de Lyon
      • Lyon, France, 69003
        • Service d'urgences médicales et chirurgicales - Hôpital Edouard Herriot - HCL
      • Lyon, France, 69004
        • Service médical d'accueil des urgences - Hôpital de la Croix Rousse - HCL
      • Pierre-Bénite, France
        • Service d'accueil des urgences - Centre hospitalier Lyon Sud - HCL

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The population participating in the study is composed of:

  • patients admitted to the emergency department,
  • persons accompanying patients,
  • professionals of the emergency departments (nurses, MD, administrative staff).

Description

Inclusion Criteria:

  • Patient aged 18 years or older.
  • Registered at the reception of the emergency department between 8 am and 8 pm, excluding bank holidays.

Exclusion Criteria:

  • Patient with psychiatric disorders or impairment of judgment related to the taking of toxic substances.
  • Patients requiring medical care in less than 30 minutes (sort code).

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Control
Patients treated in emergency departments without the presence of a mediator.
Mediation
Patients treated in emergency departments with the presence of a mediator.

The mediator tasks are :

  • Be available to patients who can solicit him and respond to their requests for information, in particular on the organization of the emergency departments and on waiting times
  • Have a proactive attitude towards patients showing nervousness signs
  • Report patients expressing the will to leave the emergency departments before medical care
  • Manage conflicts between patients / accompanying persons and emergency staff and also between patients.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Incidence of violence or aggression by patients directed towards emergency staff
Time Frame: During the patient stay in the emergency department, an average of 3 hours, up to 8 hours.
The violence or aggression will be collected by professionals of the emergency department. They will be classified in 4 levels of gravity.
During the patient stay in the emergency department, an average of 3 hours, up to 8 hours.
Incidence of violence or aggression by patients's accompanying persons directed towards emergency staff
Time Frame: During the patient stay in the emergency department, an average of 3 hours, up to 8 hours.
The violence or aggression will be collected by professionals of the emergency department. They will be classified in 4 levels of gravity.
During the patient stay in the emergency department, an average of 3 hours, up to 8 hours.

Collaborators and Investigators

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

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)

November 15, 2017

Primary Completion (Actual)

June 1, 2019

Study Completion (Actual)

June 1, 2019

Study Registration Dates

First Submitted

April 28, 2017

First Submitted That Met QC Criteria

May 2, 2017

First Posted (Actual)

May 3, 2017

Study Record Updates

Last Update Posted (Actual)

December 16, 2019

Last Update Submitted That Met QC Criteria

December 12, 2019

Last Verified

December 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 69HCL17_0038

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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