Using Virtual Reality Technology to Improve Patient Experience and Quality of Care During Brachytherapy
Recruiting
N/A
Interventional Study
Endocervical Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 20 (estimated)
- Sponsor
- University of Arkansas · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Female, ≥ 18 years of age
* Histopathologic diagnosis of gynecologic cancer (endometrial, cervical, vaginal, vulvar) that requires intracavitary brachytherapy with a tandem or interstitial brachytherapy
* Able to provide written consent
Exclusion Criteria:
* Severe vision or…
Contacts