Utilization of Virtual Reality to Increase Comfort and Reduce Procedural Distress During Port Insertion Into the Body
Recruiting
N/A
Interventional Study
Oncology Patients
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 60 (estimated)
- Sponsor
- University Hospital Ostrava · Other
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About This Trial
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 Sca…
Trial Locations
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Eligibility Criteria
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 p…
Contacts