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Impact of an On-site Simulation-based Training Programme on Adherence to Standard Precautions and Healthcare-associated Infections in Adult Intensive Care

Recruitingn/aAges 18 Years - anyAllCentre Hospitalier Régional Metz-Thionville
NCT07822971 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This is a prospective, single-centre, quasi-experimental before-and-after study conducted over 18 months in an adult ICU. The study includes a 6-month pre-intervention period, a 6-month intervention period during which healthcare professionals participate in repeated in situ simulation sessions, and a 6-month post-intervention period.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patients hospitalized in the adult intensive care unit at CHR Metz-Thionville during the study period * Patients aged 18 years or older * Patients with a length of stay in the intensive care unit of 48 hours or more * Patients for whom the data necessary to assess the outcome measures are available in the electronic health record and/or hospital surveillance databases * Patients who have been informed about the use of their health data for research purposes, in accordance with the procedures established by the institution Exclusion Criteria: * Patients who, after being informed, objected to the use of their health data for this research
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What it tests

  • Simulation-based training programme
  • No intervention
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Where

1 site
CHR Metz-Thionville, Hôpital de Mercy
Metz, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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