Actively Recruiting
Advancing Discussions Using a Video-based Support Tool About End-of-life Care: the ADVISE Project
Led by The University of Texas Health Science Center, Houston · Updated on 2025-03-30
270
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a video-based support tool designed to improve communication and patient-centered outcomes in older adults who have experienced traumatic injury. This study aims to assess how effectively the video aid encourages discussions about end-of-life care and influences decisions such as code status transitions. The project is sponsored by The University of Texas Health Science Center, Houston. Participants are randomly assigned to one of two groups: one group will watch a video conversation aid that provides information about life-sustaining care and promotes further discussion with healthcare providers, while the other group will receive usual care where such discussions occur at the provider's discretion. The video is shown to patients or their surrogates within 48 hours of admission when possible. The study uses a double-blind design. During the study, researchers will monitor participants around the time of discharge (about five days after admission) for changes in code status and various health outcomes, including hospital-free days within 30 days, ICU-free days, ventilator-free days, and discharge disposition. Surveys will assess participants' understanding of survival chances after CPR, receipt of information about life-sustaining care, desire for more information, and decisional conflict. The study continues until June 2026.
CONDITIONS
Brief Title
Advancing Discussions Using a Video-based Support Tool About End-of-life Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- English or Spanish speaking
- Admitted to any level of care following trauma
- Age 65 years or older
You will not qualify if you...
- Prisoners
- Existing do not resuscitate (DNR) or do not intubate (DNI) orders
- Patients admitted while on hospice
- Patients not expected to survive over 24-48 hours
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - About 5 days
Participants receive either a video conversation aid about life-sustaining care or usual care discussions with healthcare providers during their hospital admission.
1 to 2 visits during hospital admission
Trial Site Locations
Total: 1 location
1
The University of Texas Health Science Center at Houston
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
T
Thaddeus J Puzio, MD, MS, FACS
E
Erin Fox
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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