About this trial
Engaging families in patient care during serious illness can enhance care quality, reduce social isolation, boost satisfaction, and lower healthcare costs. However, active involvement of family caregivers remains limited because there are no evidence-based tools to guide clinicians on how to include them effectively. This study will test and refine previously developed point-of-care application, Family Room, and determine its effectiveness by comparison with a control group. A series of surveys will be used to evaluate caregiver well-being, engagement and satisfaction.
Eligibility criteria
Qualifiers
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
Disqualifiers
None
Trial design
Treatments tested in this trial
- Family Room Application
Treatment groups
Sponsors and collaborators
University of Nebraska
Lead sponsor
Gordon and Betty Moore Foundation
Collaborator