Clinical Trials Directory

Trials / Completed

CompletedNCT01187758

Israeli Judicious Antibiotic Prescription Study

Can Change in Physicians' Prescribing Habits Decrease Carriage of Resistant Bacteria in the Community?

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
5,700 (actual)
Sponsor
Sheba Medical Center · Other Government
Sex
All
Age
5 Years
Healthy volunteers
Accepted

Summary

This study aims to implement judicious antibiotic prescription habits to primary care pediatricians using a multifacet educational intervention and assess two main outcomes: 1) Direct outcome - prescription rates of the physicians. 2)Indirect outcome - carriage of antibiotic resistant bacteria by the treated population, specifically nasopharyngeal S. pneumoniae, nasal S. aureus and rectal E.coli.

Detailed description

Background: Bacterial antibiotic resistance is an increasing problem. Aims: This study aims to implement judicious antibiotic prescription habits among 30 physicians and their treated population as compared to a control group of 30 physicians and their treated population. The outcomes to be measured are: 1. Change in antibiotic prescriptions to the treated patients of the intervention vs. control physicians during the study period (4years). 2. Change in carriage of antibiotic resistant pathogens, specifically nasopharyngeal penicillin resistant S. pneumoniae,nasal MRSA, and rectal quinolone resistant E. coli. Study design: All primary care pediatricians of Hashfela district of Macabbi Healthcare services who will agree to participate will be randomly assigned to an intervention or control group. The intervention group will be led by local leaders (primary care physicians from that district) and will take part in educational activities involving annual workshops and quarterly focus group meetings. The intervention is a multifacet intervention that will include guideline preparation, knowledge building, dealing with uncertainties, etc. The patients of both intervention and control physicians will be screened twice a year for carriage of the bacteria mentioned above. Cross-sectional screening of the treated population will be carried in Summer and winter for 5 consecutive years. Screening will include signing an informed consent, filling a questionnaire and screening with nasal, nasopharyngeal and rectal swabs.

Conditions

Interventions

TypeNameDescription
BEHAVIORALWorkshops and focus group meetingsMultifacet intervention that includes: Guideline preparation and implementation, preparing clinic campaign, improving knowledge about Ab resistance and diagnosis of respiratory infections

Timeline

Start date
2002-02-01
Primary completion
2005-10-01
Completion
2007-12-01
First posted
2010-08-24
Last updated
2010-08-24

Source: ClinicalTrials.gov record NCT01187758. Inclusion in this directory is not an endorsement.