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Recruiting 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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07822971). StuddyBuddy aggregates publicly available trial information.