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Nursing Education Provided After Cesarean Section Surgery.

The Effect Of Nursing Education Provided After Cesarean Section Surgery on Postoperative Pain and Anxiety Levels: A Randomized Controlled Trial

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07467304
Enrollment
80
Registered
2026-03-12
Start date
2025-12-01
Completion date
2026-06-30
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Birth, Patient Education

Brief 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.

Interventions

OTHERExperimental: Experimental: Intervention group - Training group

Group receiving routine care and nursing training.

OTHERPlacebo Comparator: Control Group- Routine care

Rutin care group

Sponsors

Namik Kemal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

randomized controlled trial

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Spielberger State-Trait Anxiety Inventory (STAI):12 weeksSpielberger State-Trait Anxiety Inventory (STAI): The state anxiety inventory determines how a person feels at a specific time. The scale is answered on a scale of "1 (none), 2 (somewhat), 3 (a lot), 4 (completely)" according to the intensity of the individual's feelings at that moment. The trait anxiety inventory, on the other hand, determines how the individual generally feels and is answered on a scale of "1 (almost never), 2 (sometimes), 3 (most of the time), 4 (always)". The state anxiety scale has 10 reverse items, and the trait anxiety scale has 7 reverse items. To calculate the scale score, the total score obtained from the direct items is subtracted from the total score obtained from the reverse items. A constant value of 50 for the state anxiety scale and 35 for the trait anxiety scale is added to the resulting number. The possible score ranges from 20 to 80. The average score is between 36 and 41. As the score increases, the level of anxiety also increases.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS)12 weeksThe VAS is used to convert certain values that cannot be measured quantitatively into numerical values. It is a 10 cm scale with pain-free resolution at one end and the most severe pain possible at the other. In the VAS, which evaluates pain intensity, pain intensity is rated on a scale of 0 to 10. "No pain" is rated as 0 points and "very severe pain" is rated as 10 points. Pain intensity is indicated as "less than 3 points" for mild pain, "between 3-6 points" for moderate pain, and "more than 6 points" for severe pain.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORDİLEK ERDEN

Namik Kemal University

STUDY_CHAIREsra Yılmaz, Master's student

Namik Kemal University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026