Can smart alerts help ICU doctors catch problems faster?
NCT ID NCT06996626
First seen Jul 02, 2026 ยท Last updated Jul 02, 2026
Summary
This study tests a computer system that scans electronic health records and generates alerts when a clinician's behavior seems unusual. The alerts are either shown to the ICU team or hidden, and researchers compare whether seeing the alerts leads to more clinical actions. About 7,445 patients in intensive care units are included. The goal is to see if real-time alerts can improve bedside decision-making.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If it works, this could point toward a way to improve patient safety by catching unusual patterns in real time.
- What could go wrong
- This is an early-stage study testing a decision-support tool, not a treatment. The alerts may not change behavior or improve outcomes.
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 7,445 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2025
- Expected to finish
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Jun 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 to 100 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All patients in the Presbyterian and Montefiore ICUs Exclusion Criteria: * None
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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.
Contacts and locations
Locations
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UPMC Montefiore
Pittsburgh, Pennsylvania, 15213, United States
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UPMC Presbyterian
Pittsburgh, Pennsylvania, 15213, United States
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Other studies related to the condition(s) this trial covers.
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