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NCT07360054Completed

Effect of Virtual Reality on Pain, Anxiety, and Vital Signs During Femoral Catheter Removal

The Effect of Virtual Reality on Pain, Anxiety, and Vital Signs During Femoral Sheath Removal After Coronary Angiography: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

Femoral catheter removal after coronary angiography is a common clinical procedure that may cause pain, anxiety, and changes in vital signs in patients. Non-pharmacological interventions are increasingly used to improve patient comfort and safety during invasive procedures. The purpose of this randomized controlled study is to evaluate the effect of a virtual reality (VR) application on pain, anxiety, and vital signs during femoral catheter removal in patients undergoing coronary angiography. Participants were randomly assigned to either a virtual reality group or a control group receiving routine care. Patients in the intervention group experienced a virtual reality application during femoral catheter removal, while the control group received standard clinical care. Pain intensity, anxiety levels, and vital signs were assessed before, during, and after the procedure. The findings of this study are expected to contribute to evidence-based nursing practice by supporting the use of virtual reality as a safe and effective non-pharmacological method to reduce discomfort during femoral catheter removal.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
3 Jan 2026
Start date
1 Sept 2025
Primary completion date
30 Nov 2025
Lead sponsor
Kirsehir Ahi Evran Universitesi
NCT number
NCT07360054

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 1 Sept 2025 to the primary completion date, 30 Nov 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of analgesics for chronic pain prior to the procedure
  • Use of anxiolytic and/or sedative medications

Other

  • Impaired orientation to time or place

Who the study is looking for

  • Age 18 years or older
  • Ability to speak and understand Turkish
  • Undergoing elective coronary angiography with femoral arterial access
  • Planned femoral sheath removal
  • Hemodynamically stable vital signs
  • No psychiatric, cognitive, visual, or hearing impairment
  • No administration of analgesics for any reason prior to sheath removal

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kayseri City Hospital
Coordinator of this site? Confirm its status
KayseriTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.