Quality of Incoming Call Handling in an Emergency Dispatch Center
CRRAQPA
Evaluation of the Quality of Incoming Call Handling Assisted by the proQA Software in the Emergency Dispatch Center of Besançon.
1 other identifier
observational
800
1 country
2
Brief Summary
The aim of Emergency Medical Dispatch (EMD) is to ensure prompt access to medical care for all at all times, initiate appropriate responses quickly, arrange suitable hospital facilities, and coordinate patient transport and hospitalization. In France, care begins with an incoming call managed by the EM Dispatchers, who collect the patient's details and assess the seriousness of the situation. This severity assessment is essential for triggering the appropriate resources: direct dispatch of first-aiders in extreme emergencies, or transfer of the call to an emergency or general practitioner. Under- or over-assessment will necessitate redirection, resulting in a loss of time and opportunity for the patient, or emergency channel congestion. Errors at this stage can impact the entire care pathway. To assist EM dispatchers, aids have been developed. Firstly, In France, a diploma course was created in 2019. Various training methods exist. Their contribution to the quality of incoming calls handling remains unevaluated. Secondly, EM centers use regulation protocols designed to guide dispatchers in call handling and identifying the seriousness of the situation. The regulation protocol used at Besançon University Hospital is ProQA (Priority Dispatch Corporation, Salt Lake City, UT, US). It uses standardized questions and records EM Dispatchers' decisions and the responses they obtain from callers. These responses are considered by ProQA, which then assigns a "severity" code to the call. The assistance provided by regulation protocols, however useful, remains insufficient. Contextual factors can complicate compliance with regulation protocols, making matching resources to needs challenging. AQUA is a software package dedicated to quality control, enabling EM Dispatcher's supervisors to rate the quality of all stages of the call-taking process. This ensures that all key questions have been asked and that they have been asked correctly. In addition, the 'severity' code obtained by the EM Dispatcher can be compared with the 'severity' code obtained by the supervisor, using a qualifying analysis method and data entry software. The calls are replayed under optimal conditions, in a calm environment and allowing supervisors to listen multiple times to ensure no information is missed. the supervisors' code is therefore the reference code. CRRAQPA study's aim is to assess the quality of incoming call handling and to identify the factors that influence this quality.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2024
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 1, 2024
CompletedFirst Posted
Study publicly available on registry
July 16, 2024
CompletedStudy Start
First participant enrolled
August 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedNovember 7, 2024
November 1, 2024
11 months
July 1, 2024
November 6, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
The proportion of incoming calls for which the 'severity' code identified by the EM dispatchers during the call and the 'severity' code identified by the supervisor after replaying the call are in agreement.
The quality of the incoming call will be assessed based on the agreement between the 'severity' code identified by the EM dispatchers during the call and the 'severity' code identified by the supervisor after replaying the call using the AQUA software. There are six possible severity codes, which will be grouped into a three-category variables corresponding to the three possible referrals (emergency physician, general practitioner, 'flash' departure).
Through study completion, the anticipated duration is 1 year
Secondary Outcomes (8)
The proportion of over- and under-rated calls.
Through study completion, the anticipated duration is 1 year
The proportion of the different training modalities received by EM dispatchers.
Through study completion, the anticipated duration is 1 year
The number of years of experience in the profession of the EM dispatchers participating in the study.
Through study completion, the anticipated duration is 1 year
The rate of answered calls within 20 s (= quality of service at 20 seconds, QS20)
Through study completion, the anticipated duration is 1 year
The number of calls per hour in the call centre.
Through study completion, the anticipated duration is 1 year
- +3 more secondary outcomes
Eligibility Criteria
We will study incoming calls in the EMD of Besançon University Hospital. These calls must be handled by a professional EM dispatcher and must have a 'severity' code that is not unfounded. During the replay and evaluation, it can happen that the supervisor is unable to assign a severity code with certainty. This occurs when a decisive question regarding the severity code has not been asked, and the information has not been provided spontaneously by the caller. In such cases, the supervisor considers the code obtained by the EMD to be unfounded
You may qualify if:
- Calls handled by a professional EM Dispatcher during the study period.
You may not qualify if:
- Calls handled by a medical student functioning as an EM Dispatcher.
- Calls for which the "severity" code is unfounded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Centre Hospitalier Universitaire de Besancon
Besançon, Franche Comté, 25000, France
University Hospital of Besançon
Besançon, Franche Comté, 25000, France
Study Officials
- PRINCIPAL INVESTIGATOR
Antoine Leclerc
University Hospital of Besançon
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 1, 2024
First Posted
July 16, 2024
Study Start
August 1, 2024
Primary Completion
July 1, 2025
Study Completion
July 1, 2025
Last Updated
November 7, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- Immediately following publication. No end date
- Access Criteria
- Researchers who submit a methodologically sound proposal approved by our research team
The data in this study are not publicly available, but reasonable requests can be made.