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Effect of Artificial Intelligence-Based Education Before Planned Cesarean Section on Surgical Fear, Anxiety, and Postpartum Comfort Levels of Primigravida Women

NCT07419529 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2026-02-19

No results posted yet for this study

Summary

This study was planned to determine the effect of artificial intelligence use before planned cesarean section on surgical fear, anxiety and postpartum comfort levels of primigravida women. The research will be conducted in an experimental design. The research will be initiated after obtaining written permission from Niğde Ömer Halisdemir University Ethics Committee, Niğde Provincial Health Directorate and Ömer Halisdemir Training and Research Hospital. Pregnant women between the ages of 18-35, who are primigravida, who applied for planned cesarean section, who have live singleton pregnancies and who are planned for spinal anesthesia will be included in the research. Before starting the research, the study will be initiated after obtaining the institutional permissions and written permissions from the pregnant women. Preliminary Assessment Form, Personal Information Form, Surgical Fear Scale, Surgical Anxiety Scale for Adult Patients, Postpartum Comfort Scale and Perianesthesia Comfort Scale will be used in data collection. Data will be evaluated in a computer environment using IBM SPSS Statistics 24 (Statistical Package for the Social Sciences for Windows) package program. Appropriate statistical analyzes will be used in data evaluation.

Conditions

  • Surgical Anxiety Scale for Adult Patients
  • Surgical Fear Scale
  • Postpartum Comfort Scale

Interventions

OTHER

individual education about cesarean surgery

Women will be given individual training about cesarean surgery.

OTHER

about cesarean surgery using artificial intelligence

Training on Caesarean section surgery with artificial intelligence

OTHER

routine maintenance of the institution

Women in this group will not be given training on any subject.

Sponsors & Collaborators

  • Nigde Omer Halisdemir University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Months
Max Age
35 Months
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-08-15
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07419529 on ClinicalTrials.gov