Empowering Veterans in Research Effectively Using Virtual Engagement Tools

NCT07741955 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100000

Last updated 2026-08-03

No results posted yet for this study

Summary

Cardiovascular disease is the leading cause of death among Veterans. Clinical trials are essential for developing better treatments, but Veterans remain underrepresented in these studies due to barriers including limited health literacy, lack of awareness, and mistrust. Current outreach approaches rely on either in-person physician conversations, which are limited by workforce constraints, or mailed letter invitations, which often fail to engage Veterans with limited health literacy. This study tests whether AI-generated video avatars can improve Veteran engagement in cardiovascular clinical trials.

Conditions

Interventions

BEHAVIORAL

AI-Generated Avatar Videos and Chatbot for Clinical Trial Outreach

Veterans randomized to the intervention arm will receive the website link where they can select their preferred Veteran avatar speaker from a diverse set of options and self-select content topics of interest. They may watch the self-directed tailored video to guide their decision to participate in the parent trial.

Sponsors & Collaborators

  • Palo Alto Veterans Institute for Research

    collaborator OTHER
  • VA Palo Alto Health Care System

    collaborator FED
  • Stanford University

    lead OTHER

Principal Investigators

  • Celina Yong, MD, MBA, MSc · Stanford University

  • Paul Heidenreich, MD · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2030-07-31
Completion
2030-07-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07741955 on ClinicalTrials.gov