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.
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The number of eligible subjects who enroll onto the study.
Timeframe: 3 weeks
The number of subjects who withdraw or are withdrawn from the study.
Timeframe: 3 weeks
The number of subjects who successfully complete the study questionnaires for satisfaction, procedural pain, and anxiety.
Timeframe: 3 weeks
The number of times a technical problem occurs with the VR distraction
Timeframe: 3 weeks