Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07203534

ONC-MM-2407: The Effect of Virtual Reality Headsets on Pain and Anxiety in the Peri and Post Bone Marrow Biopsy Period

Led by Wake Forest University Health Sciences · Updated on 2026-03-24

160

Participants Needed

1

Research Sites

105 weeks

Total Duration

On this page

Sponsors

W

Wake Forest University Health Sciences

Lead Sponsor

A

Atrium Health Levine Cancer Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this research study is to see if a virtual reality (VR) headset is useful in reducing physical discomfort and anxiety experienced by patients who are scheduled to undergo a bone marrow biopsy (BMB) and/or bone marrow aspiration (BMA).

CONDITIONS

Official Title

ONC-MM-2407: The Effect of Virtual Reality Headsets on Pain and Anxiety in the Peri and Post Bone Marrow Biopsy Period

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to understand and willingly sign informed consent
  • Age 18 years or older at time of consent
  • Scheduled for outpatient bone marrow biopsy and/or aspiration
  • Suspected or diagnosed with malignant blood disease such as leukemia or lymphoma
  • Ability to read and understand English
  • Ability to comply with study procedures for entire study duration as judged by investigator
Not Eligible

You will not qualify if you...

  • Currently prescribed painkillers or anxiety medications before the procedure
  • Known intolerance to VR devices, significant motion sickness, seizures, vestibular disorders, or certain heart conditions
  • Presence of pacemakers, defibrillators, hearing aids, or other implanted medical devices
  • Planned bone marrow biopsy via Interventional Radiology or inpatient admission

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Levine Cancer Insitute

Charlotte, North Carolina, United States, 28204

Actively Recruiting

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Research Team

C

Courtney Schepel

CONTACT

C

Cindy Varga, MD

CONTACT

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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