Using a video tool to improve end-of-life care discussions for older trauma patients
Advancing Discussions Using a Video-based Support Tool About End-of-life Care: the ADVISE Project
This study tests whether a video tool can help older trauma patients and their families have better conversations about end-of-life care preferences.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 270 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | The University of Texas Health Science Center, Houston Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT06804226 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of a video-based support tool designed to enhance communication and patient-centered outcomes for older adults who have experienced traumatic injuries. The intervention involves using a video conversation aid alongside usual care to facilitate discussions about end-of-life care preferences. The study aims to assess how well this tool can be implemented in clinical settings and its impact on patient and family satisfaction. Participants will be English or Spanish speakers admitted to any level of care following trauma.
Who should consider this trial
Good fit: Ideal candidates for this study are older adults who have sustained traumatic injuries and are admitted to a healthcare facility.
Not a fit: Patients who are not expected to survive more than 24-48 hours or those with existing DNR/DNI orders may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the quality of end-of-life care discussions for older trauma patients and their families.
How similar studies have performed: While there is limited information on similar studies, the use of video aids in healthcare communication has shown promise in enhancing patient understanding and satisfaction in other contexts.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * English or Spanish speaking * admitted to any level of care following trauma Exclusion Criteria: * Prisoners * Existing do not resuscitate (DNR)/do not intubate (DNI) * Patients admitted while on hospice * Patients not expected to survive over 24-48 hours
Where this trial is running
Houston, Texas
- The University of Texas Health Science Center at Houston — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Thaddeus J Puzio, MD, MS, FACS — The University of Texas Health Science Center, Houston
- Study coordinator: Thaddeus J Puzio, MD, MS, FACS
- Email: Thaddeus.J.Puzio@uth.tmc.edu
- Phone: 713-500-7218
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.