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Search / Trial NCT06436014

Evaluation of the Effect of Virtual Reality Application on Postoperative Pain and Anxiety in Women Aged 50-70

Launched by OSMANIYE KORKUT ATA UNIVERSITY · May 28, 2024

Trial Information

Current as of July 03, 2025

Not yet recruiting

Keywords

Virtual Reality (Vr) Postoperative Pain Pain Management Patient Experience

ClinConnect Summary

This clinical trial is studying how virtual reality (VR) can help manage pain and anxiety in women aged 50 to 70 after certain surgeries, like knee replacements or hysterectomies. The idea is that by using VR, patients can be taken to a different, relaxing environment, which may help distract them from pain and reduce feelings of anxiety during their recovery. Proper pain management is important because it can affect how quickly someone can go home from the hospital and their overall satisfaction with their care.

To participate in this trial, women must be between 50 and 70 years old, have good vision and hearing, and be scheduled for elective surgery. They should be able to speak and understand Turkish and must have a certain level of pain after surgery, as measured by a simple scale. However, those with chronic pain, severe anxiety, or certain medical conditions that could make using VR difficult are not eligible to join. This study is not yet recruiting participants, but it aims to explore a new way to improve recovery for women undergoing these common surgeries.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Being between the ages of 50-70,
  • Being female,
  • Having adequate vision and hearing,
  • Having American Society of Anesthesiologists (ASA) physical status classification I and II,
  • Undergoing elective total knee replacement or hysterectomy surgery,
  • Having a similar analgesia protocol,
  • Being on the first postoperative day,
  • Scoring 5 or higher on the Visual Analogue Scale (VAS) assessment,
  • Being able to speak and understand Turkish.
  • Exclusion Criteria:
  • Having chronic pain,
  • Scoring below 5 on the Visual Analogue Scale (VAS) assessment,
  • Experiencing vertigo or motion-sensitive nausea,
  • Being diagnosed with severe anxiety by a specialist physician,
  • Having claustrophobia,
  • Having head or neck conditions that prevent wearing virtual reality goggles,
  • Having a Glasgow Coma Score \<15,
  • Having psychiatric, cognitive, or neurological impairments,
  • Having visual or hearing impairments.

About Osmaniye Korkut Ata University

Osmaniye Korkut Ata University is a leading academic institution dedicated to advancing research and education in the field of health sciences. As a clinical trial sponsor, the university emphasizes rigorous scientific inquiry and ethical standards, fostering collaborations that enhance the development of innovative therapeutic interventions. With a focus on improving patient outcomes and public health, the university leverages its multidisciplinary expertise and state-of-the-art facilities to support clinical research initiatives that address pressing health challenges. Through its commitment to excellence, Osmaniye Korkut Ata University aims to contribute significantly to the global body of medical knowledge and practice.

Locations

Merkez, Osmani̇ye, Turkey

Merkez, Osmani̇ye, Turkey

Merkez, , Turkey

Merkez, , Turkey

Patients applied

0 patients applied

Trial Officials

Songül GÜNGÖR, Phd

Principal Investigator

Osmaniye Korkut Ata University

Ayşe TAŞTEKİN, associate professor

Study Director

Afyonkarahisar Health Sciences University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported