Development and Validation of a Regional Multi-scale System for the Prediction of the Patient Flow in the Emergencies and the Need for Hospitalization (PRED-URG)
21. marts 2022 opdateret af: Assistance Publique - Hôpitaux de Paris
Development and Validation of a Regional Multi-scale System in Ile-de-France for the Prediction of the Patient Flow in the Emergency Department and the Need for Hospitalization
The main objective of this retrospective study is to validate a prediction system of emergencies department (ED) attendance on a wide range of time and the need for hospitalization, at various levels of perimeter (with all emergency departments or one ED in particular), with all patients or with one sub-group of patients (age, gravity, care).
Studieoversigt
Status
Rekruttering
Betingelser
Detaljeret beskrivelse
As secondary objectives, the study aims:
- to measure the influence of different factors as environmental or structural and to identify the modifiable factors, then to allow us to test by simulation, impact of various interventions (for example: opening of hospitals and reinforcement of ED teams) on arrival flows or regenerated tension inside ED teams.
- to study the relation between the flows (arrival patients, hospitalized patients) and the time of ED visit or the indicators of tension of ED team.
- Typology of ED in the region of Paris permitting afterward comparison the benchmarking type between similar structures.
This retrospective study will be performed on database: individual data in the region of Paris of summation of ED visits and data on the structures of health cares, as well as environmental data (principal given cares, weather, moves, circulations, pollution, strikes, vacations, etc.)
Undersøgelsestype
Observationel
Tilmelding (Forventet)
18000000
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Mathias WARGON, MD
- Telefonnummer: +33 1 49 83 10 86
- E-mail: m.wargon@ch-bry.org
Studiesteder
-
-
Val-de-Marne
-
Bry sur Marne, Val-de-Marne, Frankrig, 94360
- Rekruttering
- Emergency Department - Bry sur Marne Hospital
-
Kontakt:
- Mathias WARGON, MD
- Telefonnummer: +33 1 49 83 10 86
- E-mail: m.wargon@ch-bry.org
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Adults or children who have been recorded as patients in emergency departments between 2010 and 2015 are all eligibles with unlimited number of care.
85 Health Facilities in Ile de France who have emergency departments will participate the study.
Beskrivelse
Inclusion Criteria:
- All subjects have been recorded as patients in emergency departments between 2010 and 2015.
Exclusion Criteria:
- None
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Prediction of emergency department visits
Tidsramme: throughout the study, an average of 18 months
|
Calculated base on regional database: individual data of summation of ED visits in the region of Paris and structural data of health cares
|
throughout the study, an average of 18 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Prediction by age
Tidsramme: throughout the study, an average of 18 months
|
By sub-group of child or senior
|
throughout the study, an average of 18 months
|
|
Prediction by lever of gravity
Tidsramme: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
|
Prediction by type of care
Tidsramme: throughout the study, an average of 18 months
|
By type : (medical, surgical or intensive) care
|
throughout the study, an average of 18 months
|
|
Prediction by need of hospitalization or no
Tidsramme: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
|
Relation between flow of patients and indicator of tension of team
Tidsramme: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
|
Relation between flow of patients and time of ED visit
Tidsramme: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
|
|
Typology of ED of the region of Paris
Tidsramme: throughout the study, an average of 18 months
|
throughout the study, an average of 18 months
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Mathias WARGON, MD, Emergency Department - Bry sur Marne Hospital
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. juni 2021
Primær færdiggørelse (Forventet)
1. december 2023
Studieafslutning (Forventet)
1. december 2023
Datoer for studieregistrering
Først indsendt
6. februar 2017
Først indsendt, der opfyldte QC-kriterier
9. februar 2017
Først opslået (Faktiske)
14. februar 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. marts 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. marts 2022
Sidst verificeret
1. marts 2022
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NI15018
Plan for individuelle deltagerdata (IPD)
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