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โ† Trials
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Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During Port Insertion Into the Body

RecruitingNAAges 18 Years - anyAllUniversity Hospital Ostrava
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Patients \> 18 years of age * Signed Informed Consent Form * Patients Indicated for oncology treatment administration using subcutaneous port Exclusion Criteria: * Not signing of the Informed Consent Form * Patients \< 18 years of age * Patients unsuitable for subcutaneous port implantation
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What it tests

  • Virtual reality intervention
  • Standard Care (in control arm)
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Where

1 site
University Hospital Ostrava
Ostrava, Czechia
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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