Can a dashboard predict behavioral emergencies before they happen?
NCT ID NCT07746661
First seen Aug 05, 2026 · Last updated Aug 06, 2026 · Updated 1 time
Summary
This trial tests a clinical decision support tool that uses electronic health record data to predict which hospital patients are at higher risk of needing a Behavioral Emergency Response Team (BERT) within the next 48 hours. The tool displays a risk-stratified patient list in an Epic dashboard for providers over a 3-month period. The goal is to help clinicians identify high-risk patients earlier and plan proactive interventions. The study includes adult inpatients admitted to participating hospital units.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A clinical decision support tool that uses electronic health record data to predict behavioral emergency risk
- What this could lead to
- If successful, this tool could help hospitals identify at-risk patients earlier and improve proactive behavioral health care.
- What could go wrong
- This is a small, early quality improvement project, so results may not apply broadly. The tool's predictions may not always be accurate.
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.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2027
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.
Who is studied
Hospitalized adult inpatients cared for in clinical units at NYU Langone Health.
- 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: * Adult inpatients aged 18 years or older * Admitted to participating hospital unit(s) during the study period Exclusion Criteria: * Patients younger than 18 years * Patients not admitted to participating unit(s) * Patients admitted outside the 3-month implementation period * Encounters without sufficient clinical data to calculate or display a BERT prediction score
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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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NYU Langone Health
New York, New York, 10016, United States