Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
ID06804226

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

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • English or Spanish speaking
  • Admitted to any level of care following trauma
  • Age 65 years or older
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

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

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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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