Nursing Education Provided After Cesarean Section Surgery.

Enrolling by invitation · Not applicable · Has a placebo group

Conditions studied: Cesarean Birth, Patient Education

In brief

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.

Key facts

Study ID

NCT07467304

Run by

Namik Kemal University

People needed

80

Starts

2025-12-01

Expected to finish

2026-06-30

Last updated by the study team

2026-03-12

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Women aged 18-45
• Women who have undergone cesarean section
• Women who agreed to participate in the study

You may not qualify if…

• Women who are not between 18 and 45 years of age
• Women who have not had a cesarean section
• Those who did not agree to participate in the study

Where it is running

• Tekirdag Namık Kemal University — Tekirdağ, Namık Kemal Street, Turkey (Türkiye)

Full record on ClinicalTrials.gov

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