Clinical Trial

Virtual Reality and Cryotherapy for Postoperative Pain and Anxiety After Cesarean Section

Study acronym: VRCSTrail
Not Yet Recruiting
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Summary
This randomized controlled trial aims to evaluate the effectiveness of virtual reality and cryotherapy, used separately and in combination, in reducing postoperative pain and anxiety among women undergoing cesarean section under spinal anesthesia. Participants will be randomly assigned to one of three intervention groups or a control group according to the study design. Postoperative pain and anxiety will be assessed using validated measurement tools at predetermined time points after surgery. The findings of this study may provide evidence for safe, non-pharmacological interventions to improve postoperative recovery and patient comfort following cesarean section.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-06.
Trial Details
NCT Number NCT07696949
Lead Sponsor Shahid Beheshti University of Medical Sciences
Conditions Postoperative Pain, Anxiety, Cesarean Section Complications
Enrollment 120 participants
Start Date 2026-07-12
Primary Completion 2026-09-12 (estimated)
Study Completion 2026-10-12 (estimated)
Updated on ClinicalTrials.gov 2026-07-14