Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Patient under legal protection
AI-Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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