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 — DEVICE
    The 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 A
    VR distraction occurring visits 1 and 2 with normal SOC therapy at visits 3 and 4.
  • Experimental: Sequence Group B
    VR distraction occurring visits 1 and 4 with normal SOC therapy at visits 2 and 3.
  • Experimental: Sequence Group C
    VR distraction occurring visits 3 and 4 with normal SOC therapy at visits 1 and 2.
  • Experimental: Sequence Group D
    VR 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

Locations (1)

FacilityCityStateZIPSite coordinators
University of Arkansas for Medical SciencesLittle RockArkansas72205
Joseph A Holley
501-686-8274
Matthew R Kovak
501-686-8274

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