AI tutor trained on hospital protocols may sharpen ICU skills
NCT ID NCT07692035
First seen Jul 09, 2026 · Last updated Jul 10, 2026 · Updated 1 time
Summary
This trial compares two ways of using AI to help new ICU residents learn: a specialized AI tutor (ICU-Tutor) that only answers based on the hospital's own approved protocols, versus free use of general AI tools like ChatGPT. About 44 first-time ICU residents will be randomly assigned to one of the two groups. The goal is to see which approach reduces mental workload and improves how quickly and accurately residents complete ICU tasks. Results could guide how AI is used in medical training.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ICU-Tutor AI Agent
- What this could lead to
- If effective, this approach could improve how medical trainees learn complex ICU protocols, potentially reducing errors and improving patient care.
- What could go wrong
- This is a small, single-center trial with 44 participants, so results may not apply broadly. The AI tutor is limited to one hospital's protocols, and its benefits over general AI tools may be modest or absent.
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 44 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Jul 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 40 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: 1. First-time rotating residents with no prior formal ICU clinical rotation experience 2. Scheduled to complete a minimum of 4 consecutive weeks of ICU training 3. Able to complete all scheduled assessments at Day 3, Day 7, and Day 14 post-randomization 4. Possess basic digital literacy to operate assigned AI tools on standard clinical devices 5. Voluntarily provide written informed consent to participate in the trial Exclusion Criteria: 1. Cumulative prior formal ICU clinical experience exceeding 7 calendar days 2. Regular daily clinical use of AI tools for medical decision-making in the 3 months preceding enrollment 3. Physical or cognitive impairment that prevents completion of trial assessments 4. Inability to provide written informed consent
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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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Peking Union Medical College Hospital ICU Units
RECRUITINGBeijing, Beijing Municipality, 100730, China