VR-based intervention to reduce anxiety and pain during colposcopy in women

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized trial tests a virtual reality-based intervention for women undergoing colposcopy. Participants are adults 18 and older with a scheduled procedure and specific cervical cytology results, who are able to read Turkish. The study compares a VR distraction approach to a control condition to see if the VR experience lowers anxiety, stress, and pain during the procedure. It uses non-pharmacologic distraction to potentially improve the patient experience and procedure tolerance.

Why it matters

Who can join: the full rules

Inclusion Criteria:

Be 18 years of age or older, Have colposcopy scheduled due to a cervical cytology result of LSIL, HSIL, ASC-US, or HPV positivity, Be able to read and understand Turkish, Provide voluntary written informed consent -

Exclusion Criteria:

Diagnosis of a mental disorder Severe visual impairment, claustrophobia, cognitive impairment History of severe motion sickness (cybersickness) associated with virtual reality use Use of anxiolytic/analgesic medication prior to the procedure Individuals with severe cognitive impairment or communication difficulties

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Where it's running

• Çukurova University Hospital
  Adana, Adana, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: ÇİLER ÇOKAN DÖNMEZ, PhD
• Email: cilerdonmez@hotmail.com
• Phone: +903443001000

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.