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AI writes ICU updates for families: will it help?

NCT ID NCT06969196

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This pilot study tested whether AI-generated daily written summaries can help ICU clinicians communicate better with families. Clinicians edited the AI summaries before giving them to families. The study involved 27 participants and measured how acceptable and feasible this approach was for both clinicians and families.

What this could mean

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

Active substance
AI-generated written summaries
What this could lead to
If successful, this could provide a time-saving way for ICU clinicians to keep families informed daily, potentially improving communication and reducing stress.
What could go wrong
This is a very small pilot study with only 27 participants, so results may not apply broadly. The AI summaries still need clinician editing, and the approach may not work for all communication challenges.

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

27 people

The number who actually took part.

Started

Jul 2025

Finished

Oct 2025

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.

Surrogate Inclusion * One self-identified adult decision maker for an adult medical ICU patient cared for on the 10W ICU * Member of the primary ICU team believes the respective patient will require at least three additional days of ICU care * Member of the primary ICU team has identified at least one communication challenge with the patient's surrogate(s) including but not limited to: 1. Complex medical issues requiring frequent updates to families 2. Complex family dynamics (i.e., multiple involved family members) 3. Increased anxiety/stress of surrogate(s) 4. Difficult to provide updates to family members because they do not visit ICU regularly or are hard to reach by phone Surrogate Exclusion * Surrogate cannot read or understand English * Surrogate is unwilling or unable to participate in study procedures * Patient is decisional and refuses to allow surrogate participation Clinician Inclusion • Advanced practice provider (APP) on the medical ICU team on the 10W ICU Clinician Exclusion • 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

  • Rush University Medical Center

    Chicago, Illinois, 60612, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.