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Recruiting Not applicable

Optimal Implementation of Antimicrobial Stewardship in General Practice

NCT06953804 · tracked via the Priya Life Science Australia tracker
Sponsor
University of Wollongong
Phase
Not applicable
Started
2025-07-01
Last updated
2026-05-12

Condition(s) studied

The Use of Antimicrobial Stewardship in in General Practice (Family Medicine)Respiratory Tract Infections (RTI)

Investigational drug(s) / intervention(s)

Antimicrobial stewardship activities delivered through Virtual NetworkAntimicrobial stewardship activities delivered through Integrated Network activities

Antimicrobial stewardship activities delivered through Virtual Network: Participants will receive online self-paced education modules regarding antimicrobial interventions, guided self-audit and reflection regarding intervention use, and reinforcement podcasts (\~7 hours). Participants in the Virtual Newtwork arm will primarily receive these interventions online.

Antimicrobial stewardship activities delivered through Integrated Network activities: Participants will receive online self-paced education modules regarding antimicrobial interventions, guided self-audit and reflection regarding intervention use, and reinforcement podcasts (\~7 hours). Participants in the Integrated Network arm will primarily receive these interventions face-to-face and active online activities.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Study sites Inclusion Criteria: 1. New South Wales, Queensland, Tasmania, or Victoria 2. at least two GPs per practice consent to be in the study, 3. that at least one member of practice staff consents to be in the study 4. that a staff member from the site will be available to provide 90 minutes per fortnight of administrative support for the study. There are no exclusion criteria in addition to this. Exclusion Criteria: None Participating doctors and healthcare workers Inclusion criteria: 1\) Working at a participating practice for at least three days a week. Exclusion criteria : None Patients completing patient reported outcome measure survey Inclusion criteria: 1. patients consulted with a participating GP for a RTI, 2. patients re-consulted with a GP or was hospitalized. Exclusion criteria: None Patient reported experience measures survey Inclusion criteria: 1\) patient consulted with a participating GP for an RTI. Exclusion criteria: None Patients participating in interviews as part of the nested case studies Inclusion criteria: 1. consulted with a participating GP for a RTI, 2. completed a patient survey, 3. able to read and speak English Exclusion criteria: None

Primary outcome measure(s)

  • Change in use of antimicrobial interventions per 100 consults — From baseline for 5 months, from post intervention for 5 months
    This score is derived from the number of times an intervention is used (measured using the AMS Toolbox online form) divided by the number of participants a doctor sees (measured using an audit). Measuring periods are fortnightly. The eligible range is 0-100, with higher values indicating a better outcome.

Trial sites (4)

FacilityCityRegionStatus
University of Wollogongong Wollongong New South Wales Recruiting
Bond University Gold Coast Queensland Recruiting
University of Tasmania Hobart Tasmania Recruiting
Monash University Melbourne Victoria Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06953804 on ClinicalTrials.gov ↗ ← All trials in Australia