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NCT07822971
Impact of an On-site Simulation-based Training Programme on Adherence to Standard Precautions and Healthcare-associated Infections in Adult Intensive Care
Conditions: Cross Infection
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 1000
Sponsor: Centre Hospitalier Régional Metz-Thionville
Location: CHR Metz-Thionville, Hôpital de Mercy Metz
Summary
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.
Eligibility Criteria
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
Source: ClinicalTrials.gov (NCT07822971). StuddyBuddy aggregates publicly available trial information.