Using Virtual Reality Technology to Improve Patient Experience and Quality of Care During Brachytherapy
Part of paid clinical trials in Little Rock, Arkansas.
- Sponsor
- University of Arkansas
- Study ID
- NCT05440760
- Status
- Recruiting
Conditions
- Endocervical Cancer
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- The Oculus Quest 2 Virtual Reality Headset — DEVICEThe hardware includes the wireless headset with integrated headphones which will block the sight and sounds of the clinical setting as well as the hand controllers for the interactive VR experience, which will be delivered through any of three VR software options (subject may choose one or more from the following options): * Titans of Space® PLUS developed by Drash VR, LLC (Murrieta, CA, USA) * TRIPP® developed by TRIPP, Inc. (Los Angeles, CA, USA) * Nature Treks VR published by Greener Games (Ironbridge, England, UK)
Study Details
The primary objective is to demonstrate the feasibility of incorporating VR distraction into the brachytherapy and radiotherapy clinical workflow. The secondary objective is to determine if VR distraction during brachytherapy treatment for cervical cancer improves subjects' satisfaction, procedural/acute pain, and need for analgesics or anxiolytics.
Key Dates
- Start date
- Aug 8, 2022
- Status verified
- Apr 2026
- Primary completion
- Jul 31, 2027
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Sequence Group AVR distraction occurring visits 1 and 2 with normal SOC therapy at visits 3 and 4.
- Experimental: Sequence Group BVR distraction occurring visits 1 and 4 with normal SOC therapy at visits 2 and 3.
- Experimental: Sequence Group CVR distraction occurring visits 3 and 4 with normal SOC therapy at visits 1 and 2.
- Experimental: Sequence Group DVR distraction occurring visits 2 and 3 with normal SOC therapy at visits 3 and 4.
Primary Outcome Measure
The number of eligible subjects who enroll onto the study. [ Time Frame: 3 weeks ]
Central Contacts
- Joseph A Holley501-686-8274
- Vernon Sincere501-686-8274
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Arkansas for Medical Sciences | Little Rock | Arkansas | 72205 |
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