Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Completed NCT07648134

Virtual Reality for Pain Reduction During IUD Insertion

Conditions: Pain During Intrauterine Device Insertion, Anxiety

Sex: Female
Ages: 18 Years – 45 Years
Healthy volunteers: No
Phase: NA
Enrollment: 90
Sponsor: Tanta University

Location: Tanta University Hospital Tanta

Summary

This study aims to evaluate the effectiveness of virtual reality (VR) as a non-pharmacological distraction intervention during intrauterine device (IUD) insertion. IUD insertion is commonly associated with pain and anxiety, which may negatively affect patient experience and acceptance of the procedure. In this quasi-experimental study, women undergoing IUD insertion were allocated into two groups: a virtual reality group receiving immersive audiovisual distraction during the procedure and a control group receiving standard care. Pain intensity and anxiety levels were assessed and compared between the two groups. The findings of this study are expected to support the use of VR as a safe, simple, and non-invasive method to reduce procedural pain and anxiety and improve patient satisfaction during IUD insertion.

Eligibility Criteria

Inclusion Criteria: * Women eligible for intrauterine device (IUD) insertion * Age between 18 and 45 years * Willing to participate and provide informed consent Exclusion Criteria: * Contraindications to IUD insertion * History of severe anxiety disorders * Previous adverse reaction to virtual reality * Refusal to participate

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07648134). StuddyBuddy aggregates publicly available trial information.