Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During Port Insertion Into the Body
Utilization of Virtual Reality to Support Patient Comfort and Reduce Stress During the Implantation of a Subcutaneous Venous Port Prior to the Initiation of Oncological Treatment
University Hospital Ostrava
60 participants
Jul 1, 2025
INTERVENTIONAL
Conditions
Summary
This randomised controlled study evaluates whether virtual reality (VR) can support patient comfort and help reduce anxiety and stress during subcutaneous venous port implantation in adult oncology patients. Patients will be assigned to standard care or standard care with VR intervention. Subjective and objective measures of stress and discomfort will be collected, including the Visual Analog Scale (VAS) for self-reported procedural discomfort, physiological parameters (blood pressure, heart rate, variability), the STAI-6 questionnaire, and salivary cortisol. The study aims to explore the potential of VR as a non-pharmacological, immersive tool to improve procedural experience and reduce psychological distress in patients undergo-ing minor oncological procedures.
Eligibility
Inclusion Criteria3
- Patients \> 18 years of age
- Signed Informed Consent Form
- Patients Indicated for oncology treatment administration using subcutaneous port
Exclusion Criteria3
- Not signing of the Informed Consent Form
- Patients \< 18 years of age
- Patients unsuitable for subcutaneous port implantation
Interventions
Patients in this study arm will receive standard care, without the use of VR.
A virtual reality device will be used in one study arm during the implantation of the subcutaneous port.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06927804