Actively Recruiting

Phase Not Applicable
All Genders
ID07359287

Impact of a Multimodal Intervention on Antibiotic Prescribing for Respiratory Infections in Primary Care: A Cluster-Randomized Trial

Led by University Hospital, Caen · Updated on 2026-01-22

4500

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Antimicrobial resistance is a major global health threat, particularly due to inappropriate antibiotic use in primary care where most antibiotics in France are prescribed. This trial evaluates a combined approach to improve antibiotic prescribing for respiratory infections, aiming to reduce treatment duration. The study compares usual care with a new bimodal intervention involving better communication about respiratory viruses and stronger collaboration between general practitioners and pharmacists. The trial includes six primary care practices randomized into two groups. The intervention group uses a Viral Infection Prescription Tool to reduce unnecessary antibiotic starts and implements a pharmacist-led review protocol to ensure prescribed antibiotic durations follow guidelines. Pharmacists discuss any non-compliant prescriptions with prescribers to adjust treatment lengths. The control group continues standard patient management without these interventions. Participants are patients consulting for upper or lower respiratory tract infections such as angina, bronchitis, pneumonia, and sinusitis. Researchers measure the total number of antibiotic treatment days prescribed at the time of prescription. The study involves ongoing monitoring of treatment durations and collaboration effects, with the goal of improving antibiotic use in primary care settings.

CONDITIONS

Brief Title

Impact of a Multimodal Intervention on Antibiotic Prescribing for Respiratory Infections in Primary Care

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient seen in consultation for an upper or lower respiratory tract infection such as angina, acute bronchiolitis, acute bronchitis, COPD exacerbation, laryngitis, acute otitis media, serous or congestive otitis, viral respiratory infection (e.g., influenza), community-acquired pneumonia, rhinitis/nasopharyngitis, or acute sinusitis
Not Eligible

You will not qualify if you...

  • Patient under legal protection

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)

Treatment

Duration - Throughout the consultation period for respiratory infections

Participants receive care according to their assigned group: either usual primary care practices without intervention, or care including a viral infection prescription tool and a collaborative protocol between general practitioners and pharmacists to optimize antibiotic prescribing.

Visits occur as needed during consultations for respiratory infections

Trial Site Locations

Total: 1 location

1

CHU CAEN Normandie

Caen, France, 14000

Actively Recruiting

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Research Team

R

Renaud Verdon, PU-PH

P

Pascal Thibon, PH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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