Status:

NOT_YET_RECRUITING

Optimal Implementation of Antimicrobial Stewardship in General Practice

Lead Sponsor:

University of Wollongong

Conditions:

The Use of Antimicrobial Stewardship in in General Practice (Family Medicine)

Respiratory Tract Infections (RTI)

Eligibility:

All Genders

18+ years

Phase:

NA

Brief 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 ...

Detailed Description

SUMMARY The OptimasGP study is a two-arm superiority cluster-randomised Hybrid type 3 pragmatic implementation trial to promote the use of antimicrobial stewardship (AMS) interventions by doctors in g...

Eligibility Criteria

Inclusion

  • Study sites
  • New South Wales, Queensland, Tasmania, or Victoria
  • at least two GPs per practice consent to be in the study,
  • that at least one member of practice staff consents to be in the study
  • 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

  • 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:
  • patients consulted with a participating GP for a RTI,
  • 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:
  • consulted with a participating GP for a RTI,
  • completed a patient survey,
  • able to read and speak English Exclusion criteria: None

Key Trial Info

Start Date :

June 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 30 2028

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT06953804

Start Date

June 1 2025

End Date

June 30 2028

Last Update

May 1 2025

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