Nursing Education Provided After Cesarean Section Surgery.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Experimental: Experimental: Intervention group - Training group, Placebo Comparator: Control Group- Routine care.
- Who it may be relevant to
- Registry conditions: Cesarean Birth, Patient Education. Basic parameters: 18 years — 45 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Effect Of Nursing Education Provided After Cesarean Section Surgery on Postoperative Pain and Anxiety Levels: A Randomized Controlled Trial
Overview
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.
Interventions
- Other Experimental: Experimental: Intervention group - Training group
Group receiving routine care and nursing training. - Other Placebo Comparator: Control Group- Routine care
Rutin care group
Primary outcome measures
- Spielberger State-Trait Anxiety Inventory (STAI): [Time frame: 12 weeks]
Secondary outcome measures (1)
- Visual Analog Scale (VAS) [Time frame: 12 weeks]
Eligibility criteria
Inclusion criteria
- Women aged 18-45
- Women who have undergone cesarean section
- Women who agreed to participate in the study
Exclusion criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Other
Study locations
Turkey (Türkiye) · 1 center
- Tekirdag Namık Kemal University — Tekirdağ
Identifiers
NCT: NCT07467304 · DERDEN-5