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Effectiveness of Virtual Reality in the Management of Anxiety for Patients Undergoing Radiotherapy

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to evaluate the use and functionality of virtual reality (VR) during radiation therapy treatments for patients with prostate, breast, lung, or head and neck cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants planned for radiation therapy for 15 or more treatments with non-neutron generating energies (10 MV or less) per study PI for prostate, breast, lung, or head and neck cancer. Neutrons have the potential to damage the VR headset device and are generated for energies above 10 MV.

• Age 18 years or older at the time of consent.

• Eastern Cooperative Oncology Group (ECOG) performance status of 0-3 at the time of enrollment.

• Ability to understand and the willingness to sign an IRB-approved informed consent document directly.

• Agreement to participate after reviewing the information sheet

• Radiation therapist at AHWFBCCC High Point who has treated at least one participant who enrolled on to the study and used the VR device.

Locations
United States
North Carolina
Atrium Health Wake Forest Baptist Hayworth Cancer Center
RECRUITING
High Point
Contact Information
Primary
Sheri Whittington
Sheri.Whittington@Advocatehealth.org
336-878-6107
Time Frame
Start Date: 2026-05-07
Estimated Completion Date: 2029-02-01
Participants
Target number of participants: 54
Treatments
Other: Standard of care
Standard of care radiation therapy for prostate, lung, breast cancer without using the VR headset
Other: Virtual Reality intervention
Participants will wear the VR headset (Quest 2 by Meta) during radiation therapy
Other: Radiation Therapists
Providers that administer the VR intervention
Sponsors
Collaborators: Atrium Health Wake Forest Baptist
Leads: Wake Forest University Health Sciences

This content was sourced from clinicaltrials.gov