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NCT07822971From ClinicalTrials.govRecruiting

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

Impact of an On-site Simulation-based Training Programme on Adherence to Standard Precautions and Healthcare-associated Infections in Adult Intensive Care : Prospective Quasi-experimental Before-and-after Study

  • Cross Infection

At a glance

Phase
Phase not stated
Study type
Observational
Sponsor
Centre Hospitalier Régional Metz-Thionville
Enrolment target
1,000
Started
1 March 2026
Main results due
31 August 2027
Study sites
1
Registry updated
24 September 2026

Can you take part?

  • Aged 18 years and over.
  • Open to any sex.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full 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

What this study is about

In the sponsor’s own words, from the registry.

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.

Study sites(1)

  • CHR Metz-Thionville, Hôpital de Mercy

    Metz, France

    Recruiting

Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT07822971. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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