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Recruiting NCT06666465

NCT06666465 The Effect of the Operating Room Environment on Patients Experienced With Virtual Reality Glasses Before Surgery

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Clinical Trial Summary
NCT ID NCT06666465
Status Recruiting
Phase —
Sponsor Saglik Bilimleri Universitesi
Condition Clinical Practice
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-08-15
Primary Completion 2025-12-16

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Operating Room Environment Experienced by Patients Wearing Virtual Reality Glasses Before Surgery The Effect of Surgery Experience on Surgical Fear Level and Care Perceptions

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2024-08-15 with a primary completion date of 2025-12-16.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study was planned as a randomized controlled experimental study with a pretest-posttest design to examine the effect of the operating room environment experience of preoperative patients using virtual reality glasses on the patients' preoperative surgical fear level and care perceptions.

Eligibility Criteria

Inclusion Criteria: * Being 18 years or older * Agreeing to participate in the research * Having elective cholecystectomy surgery * Knowledge of Turkish and no communication barriers * Having surgery for the first time and not having seen the operating room environment Exclusion Criteria: * Being 18 years of age or younger * Refusal to participate in the research * Having undergone surgery and having seen the operating room environment before Not knowing Turkish and having any communication barrier

Contact & Investigator

Central Contact

İmren Erer

✉ mavilik_olsun@hotmail.com

📞 05462612180

Principal Investigator

Emine Parlak, 2

STUDY CHAIR

Saglik Bilimleri Universitesi

Frequently Asked Questions

Who can join the NCT06666465 clinical trial?

This trial is open to participants of all sexes, studying Clinical Practice. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06666465 currently recruiting?

Yes, NCT06666465 is actively recruiting participants. Contact the research team at mavilik_olsun@hotmail.com for enrollment information.

Where is the NCT06666465 trial being conducted?

This trial is being conducted at İnönü, Turkey (Türkiye).

Who is sponsoring the NCT06666465 clinical trial?

NCT06666465 is sponsored by Saglik Bilimleri Universitesi. The principal investigator is Emine Parlak, 2 at Saglik Bilimleri Universitesi. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology