Rethinking staff training to fight a deadly ICU infection
NCT ID NCT07102407
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests whether a constructivist educational program, which uses small-group, interactive learning, helps nurses and cleaning staff in intensive care units better follow preventive care bundles for ventilator-associated pneumonia. Researchers will compare the rate of pneumonia among patients on ventilators in two ICUs over six months: one where staff receive the constructivist training and one where they receive routine training. The goal is to see if this teaching style improves prevention practices and lowers infection rates.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Constructivist educational program about ventilator-associated pneumonia prevention
- What this could lead to
- If it works, this training approach could reduce ventilator-associated pneumonia in intensive care units, improving patient outcomes and shortening hospital stays.
- What could go wrong
- The trial is small and early, so results may not apply broadly. The outcome depends on staff adherence and patient factors, and the study does not yet prove the training causes a lasting reduction.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 51 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2025
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * age \> 18 years * patients receiving mechanical ventilation for more than 48 hours Exclusion Criteria: * A clinical diagnosis of pneumonia at the time of admission
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Karaman Training and Research Hospital
RECRUITINGKaraman, Turkey (Türkiye)
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