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New dashboard aims to reduce information overload for ICU doctors

NCT ID NCT05937646

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 study tested whether a special dashboard called AWARE helps ICU doctors and nurses make decisions faster and more accurately than using standard electronic health records. 113 healthcare providers participated in a randomized trial where they answered clinical questions using either the dashboard or their usual system. The study measured time, accuracy, and mental effort to see if the dashboard reduces information overload.

What this could mean

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

Active substance
AWARE visualization dashboard
What this could lead to
If successful, this dashboard could help ICU providers make faster and more accurate decisions, potentially improving patient care.
What could go wrong
This is a small, completed study focused on provider performance, not patient outcomes. Results may not apply to all hospitals or clinical settings.

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

113 people

The number who actually took part.

Started

Jul 2023

Finished

May 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 to 99 years

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: ICU physicians and advanced practice providers (APPs), * active full time ICU service, * use an institutional EHR (Epic or Cerner) to deliver care, and * reads and speaks English; Residents * prior ICU rotation experience, * use an institutional EHR (Epic or Cerner) to deliver care, and * reads and speaks English; Combined Exclusion Criteria: * Non-ICU Physicians or APPs, * residents with no prior ICU experience

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Conditions

The condition(s) this trial relates to.

Information Seeking Behavior

As listed by the trial registrant

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

Contacts and locations

Locations

  • University of North Carolina at Chapel Hill

    Chapel Hill, North Carolina, 27514, United States

More trials for these conditions

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