Comparison Between Virtual Reality and Stress Ball Intervention In Managing Pain During Episiotomy Repair

This study is a four-arm randomized controlled trial designed to evaluate the effectiveness of non-pharmacological interventions for pain management during episiotomy repair among women undergoing vaginal birth. Participants will be allocated to one of four groups: virtual reality, stress ball, combined virtual reality plus stress ball, or control. The virtual reality intervention is intended to provide immersive distraction, while the stress ball offers tactile distraction; the combined group receives both interventions simultaneously. The control group receives routine care only. The primary outcome is pain intensity measured during the procedure using the Visual Analog Scale. Outcome data will be compared across groups to identify the most effective intervention for reducing pain during episiotomy repair. This study may provide evidence for practical, safe, and low-cost supportive strategies that can improve maternal comfort during childbirth procedures.

NCT Number	NCT07499011
Lead Sponsor	University of Baghdad
Conditions	Perineal Pain
Enrollment	112 participants
Start Date	2025-12-16
Primary Completion	2026-02-13 (estimated)
Study Completion	2026-02-13 (estimated)
Updated on ClinicalTrials.gov	2026-04-06