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New tablet app eases stress for ICU families

NCT ID NCT05408468

Symptom relief Sponsor: University Hospitals Cleveland Medical Center 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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 a tablet-based tool called FAMCOPE-ICU designed to help family members cope with the stress of having a loved one in the intensive care unit (ICU). The study enrolled 49 family members of ICU patients who could not make their own healthcare decisions. The main goal was to see if families found the tool acceptable and helpful.

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

49 people

The number who actually took part.

Started

Aug 2022

Finished

Jul 2023

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 89 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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.

Patient Inclusion Criteria: * 18-89 years old * Intensive Care Unit (ICU) length of stay (LOS) \>= 48 hours * No anticipated ICU LOS for next 24 hours * Unable to make healthcare decisions Family Inclusion Criteria * Identified by critical care team as legally authorized representative (LAR) * Able to speak or comprehend English * \>= 18 years old Patient Exclusion Criteria: * Less than 18 years or older than 89 years * ICU LOS \< 48 hours * Anticipated ICU discharge within next 24 hours * Able to make healthcare decisions Family Exclusion Criteria * Not identified by critical care team as the LAR * Unable to speak or comprehend English * \< 18 years old

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Conditions

The condition(s) this trial relates to.

Emotional Regulation Self-Control

As listed by the trial registrant

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

Coping skills Emotion regulation

Contacts and locations

Locations

  • University Hospitals Cleveland Medical Center

    Cleveland, Ohio, 44106, United States

More trials for these conditions

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