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Reducing Unnecessary Antibiotic Prescriptions in Primary Healthcare in Saskatchewan by Identifying High Prescribers

S

Saskatchewan Health Authority

Status

Withdrawn

Conditions

Upper Respiratory Tract Infections

Treatments

Behavioral: Audit and Feedback Letter

Study type

Interventional

Funder types

Other

Identifiers

NCT05557214
REB-22-38

Details and patient eligibility

About

Approximately 90% of antibiotics are prescribed in primary healthcare (PHC) in Canada (Public Health Agency of Canada, 2020), making this an important sector for antimicrobial stewardship. Upper respiratory tract infections (URTIs) represent a common indication in PHC for which antibiotics are often prescribed unnecessarily (Leis et al, 2020; Schwartz et al., 2020). Reducing unnecessary antibiotic treatment in this sector is a vital part of contributing to minimizing the global burden of antibiotic resistance.

The goal of this research project is to reduce the number of antibiotic prescriptions among family physicians identified as high prescribers in Saskatchewan. To achieve this, the investigators will send letters to the top 25th percentile of high prescribers in PHC. The letters will contain data indicating the prescribers high antimicrobial usage as well as guidance for reducing unnecessary prescriptions and promoting appropriate lengths of prescriptions for upper respiratory tract infections.

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • must be a practicing family physician in Saskatchewan
  • top 25th percentile of antimicrobial prescribers

Exclusion criteria

  • fewer than 12 months of historical prescribing data available

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Audit and Feedback Letter
Experimental group
Description:
This group will receive 2 audit and feedback letters and a study closure letter.
Treatment:
Behavioral: Audit and Feedback Letter
No Audit and Feedback Letter
No Intervention group
Description:
This group will only receive a study closure letter.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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