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- Klinische proef NCT03881839
Internet Tools and Emergency Attendance
Impact of "Internet Tools" Consultation on Increasing Emergency Attendance
Studie Overzicht
Gedetailleerde beschrijving
It is an observational study, monocentric, prospective. This study consists in collecting data from an anonymized questioner given to patients presenting themselves at the emergency department of Clermont-Ferrand University Hospital. Answers to the questions will not change the patient's management. The questioner, containing 17 questions, requires answering "yes" or "no" by ticking boxes, or even specify when it is stipulated. This questionnaire will be given to the patient after his registration, and filled by the latter in the waiting room, pending medical care. Answering the questionnaire will take between 5 to 10 minutes. The data is anonymous.
The patient arrives at the emergency department and registers at the entrance desks where a paper and computer file is created. Then, the Reception and Orientation Nurse takes care of the patient by welcoming him in the reception box, she realizes the taking of the hemodynamics constants, the collection of the reason of consultation with the grievances of the patient. During this phase, patient will be inform of the completion of this study and asked to participate in this study. If the patient agrees to participate, an anonymized questioner will be provided and explained by one of the investigating physicians or associated partners.
Studietype
Inschrijving (Verwacht)
Contacten en locaties
Studie Locaties
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Clermont-Ferrand, Frankrijk, 63003
- Werving
- CHU clermont-ferrand
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Hoofdonderzoeker:
- Farès Moustafa
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Bemonsteringsmethode
Studie Bevolking
Beschrijving
Inclusion Criteria:
- Any major patient presenting to the emergency department by their personal way.
Exclusion Criteria:
- Suspicion of acute alcoholism
- dementia
- guardianship / trusteeship
- language barrier, non-communicating patient
- patient refusing to participate in the study
- patient with confusion
- patient with Glasgow scale less than 15
- patient not affiliated with social security
- patient not knowing how to read or write.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Observatiemodellen: Cohort
- Tijdsperspectieven: Prospectief
Cohorten en interventies
Groep / Cohort |
Interventie / Behandeling |
|---|---|
|
patient in emergency department
|
The objective of this research will be to assess, in patients presenting in an emergency department, the prior consultation of medical information on a website, the impact on the emergency consultation decision and the relevance of this consultation.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Rate of justified nature of the consultation between patient who did consult a website before the emergency room and those who didn't.
Tijdsspanne: at day 1
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The comparison between the justification (or not) of the transition to adult emergencies and the consultation of an upstream website will be done using the Chi2 test (or Fisher's exact test if applicable). The search for criteria related to the justified nature of this emergency procedure will be done with the Chi2 test (or Fisher's exact test if applicable) for the categorical data and with the Student's test (or Mann and Whitney test if not normally distributed) for continuous data. |
at day 1
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Prevalence of Internet consultation among patients admitted to emergency room
Tijdsspanne: at day 1
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The rate of consultation of a website before the emergency room, will be expressed as a percentage with its 95% confidence interval
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at day 1
|
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The rate of justified consultation
Tijdsspanne: at day 1
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The rate of justified consultation to emergency department, will be expressed as a percentage with its 95% confidence interval.
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at day 1
|
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Risk factors related to consultation of a website medical information prior to the transition to adult emergencies.
Tijdsspanne: at day 1
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The comparison between patients who visited a medical information website (vs those who did not consult the internet) before the emergency department visit will be done using the same methods as for the analysis of the main criterion.
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at day 1
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Fares MOUSTAFA, University Hospital, Clermont-Ferrand
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Verwacht)
Studie voltooiing (Verwacht)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- CHU-431
- 2019 / CE 06 (Andere identificatie: 2019 / CE 06)
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
product vervaardigd in en geëxporteerd uit de V.S.
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