Actively Recruiting

Phase Not Applicable
All Genders
ID07396428

Effectiveness and Implementation of a National Guideline for Acute Respiratory Tract Infections to Reduce Antibiotic Prescribing in Swiss Primary Care: the ImpProGUIDE Hybrid Type II Effectiveness-implementation Trial

Led by Center for Primary Care and Public Health (Unisante), University of Lausanne, Switzerland · Updated on 2026-02-09

200

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

Sponsors

C

Center for Primary Care and Public Health (Unisante), University of Lausanne, Switzerland

Lead Sponsor

U

University of Zurich, Institute for Implementation Science in Health care

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating whether implementing new Swiss national guidelines for acute respiratory infections (ARI) can reduce antibiotic prescribing in primary care. The study focuses on family doctors in French- and Italian-speaking regions of Switzerland, where many antibiotics prescribed may not be needed, especially for viral infections. The guidelines promote targeted use of point-of-care C-reactive protein (CRP) testing and shared decision-making with patients to better manage ARIs. The study involves quality circles (small groups of family doctors) and walk-in clinics randomly assigned to either an intervention group or a control group. The intervention group will receive resources and educational sessions in autumn 2025 to support guideline use, including materials for doctors and patients. The control group will continue usual care initially and receive the same educational materials later in summer 2026. The implementation strategy includes a structured training session with presentations, guides, clinical cases, and printed leaflets. Participants will be monitored through de-identified health insurance billing data to track antibiotic prescriptions and diagnostic test use. Doctors and moderators will complete brief online surveys twice a year and may join additional interviews or group discussions. Researchers will measure antibiotic use during the influenza-like illness season and the adoption of the ARI guidelines, while exploring factors affecting guideline uptake. The study runs from May 2025 to November 2026, with data collection and evaluation throughout.

CONDITIONS

Brief Title

Effectiveness and Implementation of a National Guideline for Acute Respiratory Tract Infections to Reduce Antibiotic Prescribing in Swiss Primary Care

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing to participate in a study mainly conducted in French
  • Agreeing to participate in evaluation surveys
  • Offering general practice or primary care consultations including emergencies (for walk-in clinics)
  • Having at least five physicians in the clinic (for walk-in clinics)
  • Admission to practice charged to Swiss compulsory health insurance (for walk-in clinics)
  • Planning to be active in April 2026 (for walk-in clinics)
  • Located in cantons Vaud, Geneva, Valais, Fribourg, Jura, Neuchatel, Bern, Ticino
  • Serving mainly adult patients (for walk-in clinics)
  • Registered primary care physicians participating in a quality circle or outpatient clinic in the study
  • Specialist title in general internal medicine or practicing physician
  • Willing to participate in a study mainly conducted in French (for physicians)
  • Agreeing to participate in evaluation surveys and interviews (for physicians)
Not Eligible

You will not qualify if you...

  • Quality circles without any physician included in the study
  • Physicians planning to retire before April 2026

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 6 months (influenza-like illness season)

Participants undergo a multifaceted implementation strategy including a structured educational session on acute respiratory infection guidelines to support clinical decision-making about antibiotic use.

1 baseline visit and periodic visits during the 6-month season

Long-term Monitoring

Duration - 12 months

Participants are observed for monthly antibiotic prescribing rates and adoption of guidelines over 12 months.

Monthly visits or assessments

Trial Site Locations

Total: 1 location

1

Unisanté

Lausanne, Canton of Vaud, Switzerland, 1011

Actively Recruiting

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Research Team

J

Jelena Dunaiceva, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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Published Research Related To This Trial

Systematic method for developing tailored strategies for implementing point-of-care procalcitonin testing to guide antibiotic prescribing in Swiss primary care: a protocol for a mixed-methods participatory approach.

Aline Wolfensberger, Sophie Cl Gendolla, Jelena Dunaiceva...

https://pubmed.ncbi.nlm.nih.gov/40044189