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Study identifier: NCT06953804 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Optimal Implementation of Antimicrobial Stewardship in General Practice

Condition: Respiratory Tract Infections (RTI)  ·  Sponsor: University of Wollongong

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

This trial aims to increase the use of antimicrobial stewardship resources when treating patients with respiratory tract infections. This trial is set in Australian general practices (family medicine or primary care). The main question it aims to answer is which type of implementation activities increase the use of antimicrobial stewardship resources. Researchers will compare doctors who receive face-to-face implementation activities (the Integrated Network group) to those who received virtual or online activities (the Virtual Network group). The primary hypothesis is that there will be a difference in how often interventions are used Participating doctors will be asked to record how often they use antimicrobial stewardship resources and which interventions they prefer. Participating practices will also provide researchers data on how many patients the doctors see. Patients with respiratory tract infections who saw a participating doctor will be asked to give feedback on their experience using surveys. A subgroup of doctors, practice staff, and patients will interviewed about their experience in the study.

This description comes directly from the study's public registry record.

Talk to the study team

Colin H Cortie, PhD  ·  +67 02 4221 5610  ·  optimas-gp@uow.edu.au

Andrew Bonney, PhD  ·  andrew_bonney@uow.edu.au

Always discuss trial participation with your own doctor first.

Locations (4)

University of WollogongongWollongong, New South Wales, AustraliaRecruiting
Bond UniversityGold Coast, Queensland, AustraliaRecruiting
University of TasmaniaHobart, Tasmania, AustraliaRecruiting
Monash UniversityMelbourne, Victoria, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT06953804