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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03836534
Other study ID # PO18168
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 11, 2019
Est. completion date March 31, 2019

Study information

Verified date March 2021
Source CHU de Reims
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators would like to include patients consulting in a Accident and Emergency Department (AED) during the permanence of care the week of March 11 to 17, 2018. The data collection would concern socio-demographic data, their consultation to the AED, the follow-up given to the consultation and would take place by telephone contact of patients within 48 hours of the consultation. why patients come to the emergency room, what are they waiting for? what are their main motivations? what do they do in emergencies, do they follow the treatments and recommendations?


Description:

Study of the observance of emergency exit treatments during the permanence of care. This is a descriptive study with a prospective data collection that does not alter the management of the patient. The study is epidemiological, cross-sectional, prospective inclusion. The investigators would like to include patients consulting in a AED during the permanence of care the week of March 11 to 17, 2018. The data collection would concern socio-demographic data, their consultation to the AED, the follow-up given to the consultation and would take place by telephone contact of patients within 48 hours of the consultation. The objective is to study the follow-up given by the consultation to the emergencies, in terms of compliance, follow-up of the recommendations, the objective sought by the patient coming to the emergency department. Understand the motivation of the consultation and why the treatment was not followed where appropriate. Is there a sociodemographic explanation or is it the health network that results in the saturation of emergency services? Does the system still meet the expectations of people using it?


Recruitment information / eligibility

Status Completed
Enrollment 274
Est. completion date March 31, 2019
Est. primary completion date March 18, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - adults - consultation during the early stages of care - leaving after consultation - agrees to participate in the study Exclusion Criteria: - minor patients - permanently off care - hospitalized patients - refusal to participate in the study

Study Design


Related Conditions & MeSH terms

  • Emergencies
  • Patient Coming to the Emergency Department for Any Reason

Intervention

Behavioral:
adherence to treatment of patients coming out of emergencies
Phone contact of patients within 48 hours of the consultation

Locations

Country Name City State
France Chu Reims Reims

Sponsors (1)

Lead Sponsor Collaborator
CHU de Reims

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary adherence to treatment Number of Participants who visited of the drugstore after emergency visit 2 days