- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT03881839
Internet Tools and Emergency Attendance
Impact of "Internet Tools" Consultation on Increasing Emergency Attendance
Studienübersicht
Detaillierte Beschreibung
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.
Studientyp
Einschreibung (Voraussichtlich)
Kontakte und Standorte
Studienorte
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Clermont-Ferrand, Frankreich, 63003
- Rekrutierung
- CHU clermont-ferrand
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Hauptermittler:
- Farès Moustafa
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Probenahmeverfahren
Studienpopulation
Beschreibung
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.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Beobachtungsmodelle: Kohorte
- Zeitperspektiven: Interessent
Kohorten und Interventionen
Gruppe / Kohorte |
Intervention / Behandlung |
|---|---|
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patient in emergency department
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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.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Rate of justified nature of the consultation between patient who did consult a website before the emergency room and those who didn't.
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Prevalence of Internet consultation among patients admitted to emergency room
Zeitfenster: 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
|
|
The rate of justified consultation
Zeitfenster: 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.
|
at day 1
|
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Risk factors related to consultation of a website medical information prior to the transition to adult emergencies.
Zeitfenster: 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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Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Fares MOUSTAFA, University Hospital, Clermont-Ferrand
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Voraussichtlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- CHU-431
- 2019 / CE 06 (Andere Kennung: 2019 / CE 06)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
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