Patient Care Pathway and Factors Influencing Their Choice to Consult in the Emergency Department or an Out-of-Hours Care Service: A Comparative Study (PSP-FICU)

May 20, 2026 updated by: Centre Hospitalier de Martigues

It focuses on the patient care pathway and the factors influencing their choice to seek consultation in the Emergency Department or Out-of-Hours Care Service for issues that fall under general medicine.

In France, emergency services are increasingly overcrowded, particularly with cases that should be handled by general practitioners. This strain on the healthcare system, caused by the saturation of emergency departments, has consequences on the quality of care for true emergencies.

This study aims to better understand who these users are and why they choose the Emergency Department over other care options.

Study Overview

Detailed Description

the saturation of Emergencies is explained by the constant increase in the number of visits, the reasons for this dynamic have been studied very little. Social security emphasizes that the characteristics of patients consulting there are poorly known.

Several theses in general medicine have dealt with the relevance of the use of SAU and the difficulties encountered in these structures, but none have dealt with this subject in the Martigues basin. Likewise, if several studies question doctors, none has yet questioned, in mirror image, patients in emergency rooms and an unscheduled care center.

To try to answer these unknowns, we propose to interview both patients consulting in the Emergency Department and in the City Medical Center for reasons relating to general medicine. This comparative study aims to determine and compare these two populations while identifying the factors influencing their choice of consultation location.

Our hypotheses:

  • A significant proportion of patients consult the emergency room for non-urgent reasons, which could be taken care of by general medicine.
  • Patients consult the Emergency Department or Permanent Care Center because the attending physician is not available.
  • Patients consult the Emergency Department because they were not referred by a healthcare professional before going there.
  • Patients come to the Emergency Department because it better corresponds to their way of consuming care. (Open 24 hours a day, easily accessible.) The target population of the study corresponds to adult patients consulting spontaneously and by their own means for a reason relating to general medicine, whether at the SAU of the Martigues Hospital Center or at the Escaillon Care Center.

To be included in the study, patients must meet the following criteria:

  • Patients aged 18 and over
  • Patients who have given oral consent
  • Patients with rights covered by Social Security
  • Patients able to understand French
  • Patients consulting for any reason for consultation in general medicine

We have established a list of these reasons based on reading scientific literature and our experience in the practice of general medicine.

Study Type

Observational

Enrollment (Actual)

194

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

    • Bouches du Rhone
      • Martigues, Bouches du Rhone, France, 13500
        • CH de Martigues
      • Martigues, Bouches du Rhone, France, 13500
        • Centre Hospitalier de Martigues

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

patients who consult the emergency room vs. permanent care in the city of Martigues

Description

Inclusion Criteria:

  • Patients aged 18 and over.
  • Patients who have given oral consent.
  • Patients with rights covered by Social Security.
  • Patients able to understand French.

Exclusion Criteria:

  • Minor patient.

    • Illiterate patient.
    • Patients who do not have social security rights.
    • Patient under guardianship or curatorship.
    • Patient deprived of liberty.
    • Patient under legal protection.
    • Patients admitted for consultation for the reasons below:
  • Chest pain
  • Limb fracture/deformity
  • Major trauma
  • Wound
  • All vital emergencies: neurological, hemodynamic, respiratory.

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
group of patients consulting the Emergency Department
urgence care, permance care
group of patients consulting the permanent care service

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
prevalence
Time Frame: one days
proportion of patients consulting the Emergency Department for a reason relating to general medicine
one days

Collaborators and Investigators

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

Investigators

  • Study Director: Bouriche Bouriche, doctor, Centre Hospitalier de Martigues

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)

January 15, 2025

Primary Completion (Actual)

May 20, 2026

Study Completion (Actual)

May 20, 2026

Study Registration Dates

First Submitted

June 23, 2025

First Submitted That Met QC Criteria

June 23, 2025

First Posted (Actual)

July 1, 2025

Study Record Updates

Last Update Posted (Actual)

May 22, 2026

Last Update Submitted That Met QC Criteria

May 20, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2024_02_RIPH3_Thèse Interne Dr

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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