NCT06502925

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

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
800

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2024

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

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

Completed
15 days until next milestone

First Posted

Study publicly available on registry

July 16, 2024

Completed
16 days until next milestone

Study Start

First participant enrolled

August 1, 2024

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
Last Updated

November 7, 2024

Status Verified

November 1, 2024

Enrollment Period

11 months

First QC Date

July 1, 2024

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

RECRUITING

University Hospital of Besançon

Besançon, Franche Comté, 25000, France

RECRUITING

Study Officials

  • Antoine Leclerc

    University Hospital of Besançon

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Jean-Baptiste Pretalli, PhD

CONTACT

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

The data in this study are not publicly available, but reasonable requests can be made.

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

Locations