Actively Recruiting
Virtual Reality for Symptom Management in Patients Undergoing Hematopoietic Stem Cell Transplantation
Led by Roswell Park Cancer Institute · Updated on 2026-04-07
28
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial compares the use of virtual reality to standard care for improving symptom management in patients undergoing hematopoietic stem cell transplantation (HSCT). Significant symptoms experienced by hospitalized HSCT patients include, but are not limited to, depression, tiredness, anxiety, drowsiness, lack of appetite, pain, and overall decreased quality of life and well-being. Virtual reality (VR) as an intervention can provide these patients with a much-needed escape from their reality and has proven results in clinical settings as a distraction therapy. VR technology targets the patient's auditory, visual, and physical contact/touch senses, and has been evidenced to improve depression, fatigue, anxiety, appetite, and pain. Virtual reality may improve symptom management in patients undergoing HSCT.
CONDITIONS
Official Title
Virtual Reality for Symptom Management in Patients Undergoing Hematopoietic Stem Cell Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients (18 years or older) admitted to Roswell Park on 5 North for planned hematopoietic stem cell transplantation (HSCT)
- Must be alert and oriented (Glascow Coma Scale of 15, Nursing Universal Flowsheet) and able to consent to participate
- Expected to be admitted to Roswell Park inpatient unit for at least 1 week
- Participant must understand the investigational nature of the study and sign an approved informed consent form prior to any study procedures
You will not qualify if you...
- Known brain metastases due to poor prognosis and potential neurologic dysfunction
- Uncontrolled illnesses such as active infection, symptomatic congestive heart failure, unstable angina, cardiac arrhythmia, or psychiatric/social issues limiting compliance
- Pregnant patients
- Incarcerated patients
- Unwilling or unable to follow protocol requirements
- Prone to motion sickness, nausea, dizziness, history or risk of seizures, delirium, or confusion
- Audio or visual impairments preventing use of VR device
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Roswell Park Cancer Institute
Buffalo, New York, United States, 14263
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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