Clinical Trial

Nursing Education Provided After Cesarean Section Surgery.

Enrolling by Invitation
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Record status
This record was last updated March 12, 2026 (before its estimated May 15, 2026 completion). Its status may not reflect the trial's current state.
Summary
The aim of this study is to determine the effect of individual education given after cesarean section on the levels of pain and anxiety in women in the postoperative period. The research is a randomized controlled trial with an experimental design, featuring a pre-test-post-test control design with experimental and control groups. The study will be conducted at Çorlu State Hospital. Data will be collected by conducting a pre-test within the first 6-12 hours after cesarean section, followed by education, and then a post-test before discharge (24-48 hours later). The Demographic Information Form, Knowledge Test, Spielberger State-Trait Anxiety Inventory, and Visual Analog Scale will be used to collect data.
Trial Details
NCT Number NCT07467304
Lead Sponsor Namik Kemal University
Conditions Cesarean Birth, Patient Education
Enrollment 80 participants
Start Date 2025-12-01
Primary Completion 2026-05-15 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-03-12