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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorCenter for Primary Care and Public Health (Unisante), University of Lausanne, Switzerland

About this trial

The ImpProGUIDE study aims to find out whether implementing new Swiss national guidelines for acute respiratory infections (ARI) can help to reduce antibiotic prescribing in primary care. In Switzerland, most antibiotics are prescribed in outpatient care, and many of these prescriptions may not be needed - especially when infections are caused by viruses, which antibiotics do not treat. Reducing overuse of antibiotics is important to slow the spread of antibiotic resistance.

The new guidelines were developed by the Swiss Society for Infectious Diseases (SSI) to support family doctors in managing ARIs, based on a syndromic approach. They recommend the targeted use of point-of-care C-reactive protein (CRP) testing when bacterial infection is suspected, as well as shared decision-making with patients.

This study will be carried out in quality circles (QCs) - small groups of family doctors who meet regularly to discuss and improve clinical practice - and in walk-in clinics in French- and Italian-speaking regions of Switzerland. Each will be randomly assigned to either an "intervention" group or a "control" group.

In the intervention group, QC moderators and medical center directors will receive implementation resources to lead a session and distribute materials to their group in autumn 2025 on the new guidelines. Doctors can then decide whether or not to use the recommendations in their consultations.

In the control group, QCs and centers will continue their regular activities. They will receive access to the same educational materials later, in summer 2026.

Throughout the study, the researchers will collect de-identified data from health insurance billing records to track antibiotic prescribing and the use of diagnostic tests. Doctors and QC moderators will also be invited to complete short online surveys twice a year (10-15 minutes) and may be asked to join optional interviews or group discussions after the winter season.

The study will also explore the effectiveness of the implementation strategies on the adoption of the SSI guidelines, as well as the barriers and facilitators to adoption. This study type is known as a hybrid effectiveness implementation study, simultaneously evaluating an intervention's impact on antibiotic prescribing and the strategies used to implement the new national guidelines in a real-world setting.

Participation in the study is voluntary. Doctors can withdraw at any time. All data will be handled confidentially and in line with Swiss data protection laws.

The study is funded by the Swiss National Science Foundation. No support is received from pharmaceutical companies or manufacturers of diagnostic tests.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Willing to participate in a study mainly conducted in French

Agreeing to participate in evaluation surveys

Disqualifiers

The clinic offers general practice/primary care medicine consultations, including emergencies

The clinic includes at least five physicians

The clinic has an "Admission to practice charged to Swiss compulsory health insurance"

The clinic plans to still be active in April 2026

Trial design

Design model

Parallel

Treatments tested in this trial

  • Training Session on acute respiratory infection guideline within a multifaceted implementation strategy

    Behavioral

    Implementation strategies are deployed within quality circles, consisting of a structured educational session including a PowerPoint presentation, a facilitation guide, clinical vignettes, and printed materials for physicians and patients. The session is designed to support clinical decision-making about antibiotic use for ARI, based on targeted use of CRP and shared decision-making.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Acute respiratory infection guideline implementationExperimental treatment 1 intervention
Group B: Usual careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Defined daily doses of antibiotics commonly used for acute respiratory infections per 1000 consultations

Defined daily doses (DDD) of selected antibiotics (amoxicillin, co-amoxicillin, clarithromycin, azithromycin) per 1000 consultations, based on de-identified health insurance billing data. These antibiotics represent those most commonly prescribed for pneumonia, acute bronchitis, and upper respiratory tract infections (excluding pharyngitis, sinusitis, and otitis media).

Time frame
Over the influenza-like illness (ILI) season (6 months).
2

Penetration of acute respiratory infection guidelines

Percentage of physicians who self-declare adoption of the new acute respiratory infection (ARI) guidelines (i.e., treating patients according to the guidelines).

Time frame
Baseline and after 6 months.

Secondary outcomes

1

Monthly antibiotic prescribing rate

Monthly prescribing rates expressed as: (1) DDD of antibiotics commonly used for ARI per 1000 consultations, and (2) DDD of total antibiotics per 1000 consultations.

Time frame
Monthly for 12 months.
2

Model-estimated differences in antibiotic use

Multilevel regression coefficients estimating differences in antibiotic use (DDD per 1000 consultations) according to physician, practice, quality circle (QC), walk-in clinic, and patient characteristics.

Time frame
Over the ILI season (6 months).
3

Model-estimated differences in antibiotic use

Multilevel regression coefficients estimating differences in antibiotic use (DDD per 1000 consultations) according to physician, practice, QC, walk-in clinic and patient characteristics.

Time frame
Over 12 months.
4

Use of diagnostic tests

Number of C-reactive protein (CRP) measurements, blood counts, and chest radiographs per 1000 consultations.

Time frame
Over the ILI season (6 months).

Other outcomes

1

Knowledge about acute respiratory infection management

Knowledge about ARI management according to the new guidelines, measured with a custom questionnaire: "Knowledge questionnaire on the diagnosis and treatment of acute respiratory infections and influenza-like syndromes", (6 questions, of which 3 multiple choice, 3 single choice).

Time frame
Baseline and after 6 months.
2

Cost-effectiveness of ARI guideline implementation

Incremental cost-effectiveness ratio (ICER), expressed in CHF per percentage point reduction in antibiotic prescribing, comparing the ARI guideline implementation strategy to routine practice.

Time frame
Over the ILI season (6 months).

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

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

Lead sponsor

University of Zurich, Institute for Implementation Science in Health care

Collaborator

Anresis, Swiss Centre for Antibiotic Resistance, University of Bern, Switzerland

Collaborator

CHUV, Lausanne University Hospitals, Switzerland

Collaborator

Swiss Pharmacy Association, pharmaSuisse

Collaborator