Actively Recruiting
Cardiovascular Health Education Via Virtual Reality for Breast Cancer Survivors Receiving Anthracyclines or Trastuzumab - Phase 2
Led by Virginia Commonwealth University · Updated on 2026-05-26
30
Participants Needed
3
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a virtual reality (VR) program called Survivors' Virtual Reality Survivorship Experience (SurviVRSE) designed to educate breast cancer survivors about heart health. This study focuses on survivors who have received anthracyclines or trastuzumab, treatments known to potentially affect heart function. The goal is to test how easy, feasible, and acceptable the VR intervention is for participants, and to explore whether it improves knowledge about cancer therapy related cardiac dysfunction (CTRCD) and promotes heart-healthy behaviors like physical activity. Participants will receive access to the VR cardiovascular health education and gaming intervention during a treatment infusion. The VR content covers potentially cardiotoxic treatments, how to recognize treatment-related heart problems, and heart-healthy lifestyle changes survivors can adopt. Before starting, participants will complete a baseline survey, then go through the VR education modules and games during one infusion session. Afterward, they will complete a similar survey within two days and a final survey one month later. Throughout the study, researchers will measure participants' knowledge of CTRCD at baseline, shortly after the intervention, and four weeks later. They will also assess usability, acceptability, user satisfaction, physical activity, sleep quality, tobacco use, and intent to change behavior. The entire participation involves completing surveys around the VR session and follow-up assessments, allowing researchers to evaluate the impact of the VR program on breast cancer survivors' heart health awareness and behaviors.
CONDITIONS
Brief Title
Cardiovascular Health Education Via Virtual Reality for Breast Cancer Survivors Receiving Anthracyclines or Trastuzumab
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Able to speak and read in English
- Actively receiving trastuzumab or an anthracycline-based treatment
- Diagnosed with stages 0-III breast cancer
You will not qualify if you...
- History of prior breast cancer diagnosis (not first breast cancer diagnosis)
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 - 1 day
Participants receive a virtual reality intervention focused on cardiovascular health education and gaming during one infusion treatment. This includes completing education modules about cardiotoxic treatments, identifying cardiac dysfunction, and promoting heart healthy behaviors.
1 infusion treatment visit (in-person)
Duration - 4 weeks
Participants complete surveys to assess knowledge, usability, acceptability, user satisfaction, physical activity, sleep quality, tobacco use, and intent to change behavior immediately after the intervention and at one month post-intervention.
1 follow-up survey visit (remote)
Trial Site Locations
Total: 3 locations
1
Adult Outpatient Pavilion
Richmond, Virginia, United States, 23220
Actively Recruiting
2
Cellular Immunotherapies and Transplant Department
Richmond, Virginia, United States, 23220
Actively Recruiting
3
VCU Health at Stony Point
Richmond, Virginia, United States, 23223
Actively Recruiting
Research Team
A
Arnethea Sutton, Ph.D
V
Victoria Williams
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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