Using the Family Room App to Support Caregivers
Official title: A Phase I Clinical Trial Evaluating the Impact of the Family Room App on Caregiver Well-being, Satisfaction, and Engagement in the Intensive Care Unit
Run by University of Nebraska · NCT06463158 · Data updated 2026-11-12
This study tests whether using the Family Room app can help family caregivers feel more involved and satisfied while caring for patients in intensive care units.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 19 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | University of Nebraska Academic / other |
| Locations | 2 sites (Omaha, Nebraska and 1 other locations) |
| Status | Recruiting |
| Started | July 1, 2024 |
| Main results expected | October 31, 2026 |
| Study ends | February 28, 2027 |
| Registry record updated | August 28, 2026 |
| Trial ID | NCT06463158 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adult family caregivers who are present at the bedside of a patient in the ICU and are authorized to make medical decisions.
✕Probably not a fit
Patients whose caregivers are not authorized representatives or who are not present during the ICU admission may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of the Family Room application, a point-of-care tool designed to engage family caregivers in the care of patients in intensive care units (ICUs). By comparing caregiver experiences between those using the app and a control group receiving standard care, the study aims to assess improvements in caregiver well-being, engagement, and satisfaction. Participants will be recruited from multiple ICUs to ensure diverse representation, with a focus on enhancing the role of caregivers during serious illness. Surveys will be utilized to gather data on the impact of the application on caregivers' experiences.
Why it matters
Potential benefit: If successful, this study could significantly improve caregiver engagement and satisfaction, leading to better patient care outcomes.
How similar studies have gone: Other studies have shown positive outcomes with similar caregiver engagement tools, suggesting potential for success in this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
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
Where it's running
-
Nebraska Medicine
Omaha, Nebraska, United States Recruiting -
University of Nebraska Medical Center
Omaha, Nebraska, United States Recruiting
Study contacts
- Principal investigator: Breanna Hetland, PhD — University of Nebraska
- Study coordinator: Breanna Hetland, PhD
- Email: breanna.hetland@unmc.edu
- Phone: 309-231-4537
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.