New app aims to ease stress for ICU families
NCT ID NCT06463158
First seen Jun 25, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This study tests a mobile app called Family Room, designed to help family caregivers of ICU patients feel more engaged, satisfied, and less stressed. The app provides education, emotional support, and guidance on comfort care activities at the bedside. Researchers will compare app users to a control group using surveys, enrolling 100 adult caregivers.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Family Room mobile application
- What this could lead to
- If it works, this app could give ICU families a practical tool to feel more involved and supported at the bedside.
- What could go wrong
- This is a small, early-phase study without a drug or device that directly treats disease. The app may not improve well-being or satisfaction as hoped.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jul 2024
- Expected to finish
-
Feb 2027
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
-
19 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * 19 years of age or older * Present at participant's bedside during the intensive care unit (ICU) admission * Participant's legally authorized representative (LAR) or designated caregiver to make medical decisions on their behalf Exclusion Criteria: • Not legally authorized representative (LAR) or designated caregiver to make medical decisions on their behalf
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Engagement are added.
By submitting, you agree to our Terms of use
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
2 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
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
-
Nebraska Medicine
RECRUITINGOmaha, Nebraska, 68105, United States
-
University of Nebraska Medical Center
RECRUITINGOmaha, Nebraska, 68198, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Choose-Your-Own-Adventure comic help kids eat better and move more?
- Could outdoor play in kindergarten improve Kids' mental and physical health?
- Can a digital tool bring a personal touch to nursing home care?
- Soothing sounds: a simple audio may help Low-Birth-Weight babies thrive
- Can belief in yourself calm surgical fear?
- Could ditching diets boost Women's body image and Well-Being?