- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07046754
- Original Trial
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)
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Contacts and Locations
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
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Sponsor
Investigators
- Study Director: Bouriche Bouriche, doctor, Centre Hospitalier de Martigues
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
Clinical Trials on This Study is to Evaluate the Prevalence
-
Hacettepe UniversityCompletedThe Aim of This Study is to Evaluate the Effects of Acute Exercise on Serum Oncostatin M Levels in Healthy, Recreationally Active MalesTurkey (Türkiye)
-
Konkuk University Medical CenterCompletedThis Study Was Focused to Evaluate Feasibility of Doppler Tissue Monitoring During the Induction Anesthesia, | and Evaluate Routine Propofol Induction's Effect on Myocardial Tissue Motion, Using Non-invasive Doppler Tissue and 2D Speckle Tracking Imaging. | This is the First Study,...Korea, Republic of
-
Jinnah Sindh Medical UniversityAl Khidmat Hospital Nazimabad Karachi; Medics Laboratories (Pvt.) Ltd.CompletedThe Main Focus of This Study is to Evaluate the Safety of Zingiber Officinale L. Tablets as Hypolipidemic Agent in Hypertensive PatientsPakistan
-
Baylor College of MedicineRecruitingThe Aim of This Study is to Measure Blood Flow Before and After a BlockUnited States
-
University Hospital, GasthuisbergCompletedthe Focus of This Study is to Measure the Intra- and Interobserver Agreement for the Evaluation of Early Stage EmbryosBelgium
-
University of PennsylvaniaPhilips Medical SystemsCompletedThis Study is Being Conducted to Collect Echocardiographic Data to Test the Lumify Ultrasound With Hemodynamic Automation DeviceUnited States
-
Food and Nutrition Research Institute, PhilippinesPhilippine Council for Health Research & DevelopmentNot yet recruitingAthletes | Nutrition Physiology | The Focus of This Study is to Describe the Body Composition and Metabolism of Athletes and Non-athletes
-
Universitätsklinikum Hamburg-EppendorfRecruitingThis Study Aims to Evaluate the Safety Profile and Tissue Changes After Biostimulatory Treatments to the Face in Healthy VolunteersGermany
-
Centre Hospitalier Universitaire de NiceRecruitingThis Study is Testing the Use of MatriDermFrance
-
University of Colorado, DenverNational Cancer Institute (NCI)Active, not recruitingThe Focus of This Study is to Identify How Different Approaches to Mammography Communication Affect Skepticism Toward Mammography EvidenceUnited States
Clinical Trials on type of consultation
-
Centre Hospitalier Universitaire de NiceCompleted
-
University of Southern DenmarkUniversity of Copenhagen; University of Aarhus; Region North DenmarkCompletedQuality of Life | Life StyleDenmark
-
Vastra Gotaland RegionNot yet recruitingOsteoarthritis, Knee | Osteoarthritis, Hip
-
Universidade do PortoCompletedTrapezius Muscle StrainPortugal
-
University of Southern DenmarkOdense University Hospital; Sygekassernes Helsefond; Danish Nurses OrganisationCompleted
-
Philipps University Marburg Medical CenterUnknownHealthy ParticipantsGermany
-
NHS LothianUniversity of EdinburghTerminatedAbortion in First Trimester | Abortion EarlyUnited Kingdom
-
Hospital Israelita Albert EinsteinCompletedRespiratory Tract InfectionsBrazil
-
University of Sao Paulo General HospitalCompleted
-
Tabula Rasa HealthCareTerminated