Internet Tools and Emergency Attendance
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|ClinicalTrials.gov Identifier: NCT03881839|
Recruitment Status : Unknown
Verified March 2019 by University Hospital, Clermont-Ferrand.
Recruitment status was: Recruiting
First Posted : March 20, 2019
Last Update Posted : March 25, 2019
|Condition or disease||Intervention/treatment|
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.
|Study Type :||Observational|
|Estimated Enrollment :||431 participants|
|Official Title:||Impact of "Internet Tools" Consultation on Increasing Emergency Attendance|
|Actual Study Start Date :||March 21, 2019|
|Estimated Primary Completion Date :||March 2020|
|Estimated Study Completion Date :||March 2020|
|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.
- Rate of justified nature of the consultation between patient who did consult a website before the emergency room and those who didn't. [ Time Frame: at day 1 ]
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.
- Prevalence of Internet consultation among patients admitted to emergency room [ Time Frame: at day 1 ]The rate of consultation of a website before the emergency room, will be expressed as a percentage with its 95% confidence interval
- The rate of justified consultation [ Time Frame: at day 1 ]The rate of justified consultation to emergency department, will be expressed as a percentage with its 95% confidence interval.
- Risk factors related to consultation of a website medical information prior to the transition to adult emergencies. [ Time Frame: at day 1 ]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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03881839
|Contact: Lise LACLAUTRE||04 73 75 49 firstname.lastname@example.org|
|Clermont-Ferrand, France, 63003|
|Contact: Lise LACLAUTRE 04 73 75 49 63 email@example.com|
|Principal Investigator: Farès MOUSTAFA|
|Principal Investigator:||Farès MOUSTAFA||University Hospital, Clermont-Ferrand|