Antibiotic Education for Children in an Emergency Care Unit

Not Applicable

Completed

• Conditions: Respiratory Tract Infections; Pyelonephritis; Urinary Tract Infections; Otorhinolaryngologic Diseases

• Registration Number: NCT00948779
• Lead Sponsor: Assistance Publique - Hôpitaux de Paris

Brief Summary

The purpose of this study is to determine if a patient education in acute condition about the intake of oral solution antibiotic in children under 6 year-old are effective to improve the satisfaction about the therapeutic education, the knowledge about antibiotics among the patients' families and thereby decrease the misuses of antibiotics.

Detailed Description

Adherence to antibiotic regimen for common childhood illnesses, such as otitis media and streptococcal pharyngitis, is related to a variety of outcomes such as illness' remission, prevention of recurrent infections, maintaining of cost-effectiveness, and prevention of the growth of antibiotic-resistance. A patient and family 's therapeutic education about the intake of an oral solution of antibiotic should decrease the misuses of antibiotic, improve the family 's knowledge and the satisfaction of the patient and his family. Those factors are related to the understanding and adherence to the antibiotic prescription.

Study Timeline

• Study Start: 2009-02
• Study First Submitted: 2009-07-28
• Study First Submitted QC: 2009-07-28
• Study First Posted: 2009-07-29
• Primary Completion: 2012-03
• Study Completion: 2012-03
• Status Verified: 2012-07
• Last Update Submitted: 2023-02-01
• Last Update Posted: 2023-02-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

• French-speaking patients seen at the emergency department and discharged with a diagnosis of bacterial infections (urinary and respiratory tract infections, streptococcal pharyngitis, acute otitis media) requiring 5 to 10 days of an oral solution of antibiotic.
• Under 6 year-old.
• No opposition of the parents to be included in the study.
• Personal health insurance.

Exclusion Criteria

• Chronic pathology such as: Sickle cell disease, AIDS.
• Parents with insufficient knowledge of French.
• Family not reachable by phone.
• Antibiotic's suspected allergy.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
satisfaction (likert scale)	15 days

Secondary Outcome Measures

Name	Time	Method
Parent's knowledge	15 days and 6 months

Trial Locations

Locations (1)

Hôpital Robert Debré; 🇫🇷 Paris, France