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AI vs. nurse: which orientation keeps ICU patients calmer?

NCT ID NCT07171944

Symptom relief Sponsor: Koç University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 26, 2026 · Last updated Jun 26, 2026

Summary

This study compares an AI-powered orientation program to one given by human nurses for patients in the intensive care unit (ICU). The goal is to see if the AI program helps patients have more days without delirium, lowers anxiety and depression, and shortens their hospital stay. Ten adult ICU patients will take part, receiving orientation twice daily for three days.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
structured orientation program (AI-supported vs. human nurse)
What this could lead to
If it works, this could point toward a simple, AI-based way to reduce delirium, anxiety, and hospital stays for ICU patients.
What could go wrong
This is a very small early trial (10 people) that hasn't started yet. Results may not apply to all ICU patients, and the AI program may not outperform human nurses.

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

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

About 10 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Nov 2025

An estimate. Start dates often move.

Expected to finish

Nov 2026

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Intensive care unit confusion assessment scale (CAM-ICU scale) score of 0-2 * Age 18 years or older * Hospitalized in the intensive care unit for at least 24 hours * Glasgow coma scale score of 13-14-15 points * Richmond Agitation Sedation Scale (RASS) score between -1 and +1 * No hearing problems Exclusion Criteria: * Intensive care unit confusion assessment scale (CAM-ICU scale) score of 6-7 * Any psychiatric illness or impaired brain function * Defined hearing loss * Advanced dementia * Younger than 18 years of age * Richmond Agitation Sedation Scale (RASS) score outside the range of -1 to +1 * Who use sedative medication * History of surgery or disease around the ear

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Conditions

The condition(s) this trial relates to.

anxiety disorder delirium Depression mixed anxiety and depressive disorder Orientation, Spatial

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Anxiety and depression Artificial intelligence (AI) Critical care Delirium Intensive care units (ICUS) NURSE Orientation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Koç University

    Istanbul, 34010, Turkey (Türkiye)

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