RecruitingNot ApplicableNCT06927804

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


Sponsor

University Hospital Ostrava

Enrollment

60 participants

Start Date

Jul 1, 2025

Study Type

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether using a virtual reality (VR) headset during the placement of a subcutaneous port (a small device implanted under the skin to deliver cancer treatment) can reduce pain, anxiety, and distress during the procedure. **You may be eligible if...** - You are over 18 years old - You are scheduled to have a subcutaneous port implanted as part of your cancer treatment - You are able to give informed consent **You may NOT be eligible if...** - You are under 18 - You are not a suitable candidate for subcutaneous port implantation for medical reasons - You refuse to sign the informed consent form Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREVirtual reality intervention

A virtual reality device will be used in one study arm during the implantation of the subcutaneous port.

PROCEDUREStandard Care (in control arm)

Patients in this study arm will receive standard care, without the use of VR.


Locations(1)

University Hospital Ostrava

Ostrava, Moravian-Silesian Region, Czechia

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NCT06927804


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