Clinical trial Recruiting at 1 site Interventional Ages 18 to 40

Local ICU AI Teaching Agent to Support Rotating Residents

Official title: Effect of a Localized ICU-Specific AI Teaching Agent on Institutional Workflow Mastery and Clinical Competency in Rotating ICU Residents: A Single-Center, Parallel-Group, Randomized Controlled Superiority Trial

Run by Peking Union Medical College Hospital · NCT07692035 · Data updated 2026-11-12

A new AI tutor designed for a single center is being tested to see if it reduces cognitive load and improves ICU protocol task performance for first-time rotating residents.

Quick facts

Study typeInterventional
Ages18 Years to 40 Years
SexAll
Enrollment44 (estimated)
SponsorPeking Union Medical College Hospital
Academic / other
Locations1 site (Beijing, Beijing Municipality)
StatusRecruiting
StartedMarch 20, 2026
Main results expectedJune 30, 2026
Study endsJuly 5, 2026
Registry record updatedJuly 9, 2026
Trial IDNCT07692035 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

First-time ICU rotating residents with at least 4 consecutive weeks of ICU training and ability to use AI tools on clinical devices.

Probably not a fit

Residents with substantial prior ICU experience or those not benefiting from AI-assisted learning may see little to no improvement.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pragmatic, parallel-group randomized trial compares an institution-specific, protocol-bound AI teaching agent (ICU-Tutor) with unrestricted general-purpose AI tools. Conducted in the ICU teaching wards at Peking Union Medical College Hospital, it targets first-time rotating residents during their initial ICU rotation. The study uses a 1:1 randomization to assess whether ICU-Tutor can lower extraneous cognitive load and enhance standardized protocol performance over a 14-day period. Eligible participants will be screened, consented, and assessed at Day 3, Day 7, and Day 14 after randomization. The trial operates within routine clinical education settings and adheres to site-specific ICU protocols and workflows.

Why it matters

Potential benefit: If successful, residents may learn faster with less cognitive strain and perform ICU tasks more accurately according to local guidelines.

How similar studies have gone: Previous studies show mixed results for AI learning aids; this trial tests a site-specific AI agent designed to align with local protocols, which is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
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

Where it's running

  • Peking Union Medical College Hospital ICU Units
    Beijing, Beijing Municipality, China
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.