Visual Education for Spinal Anesthesia Acceptance

March 28, 2025 updated by: İlke Dolgun, Istinye University

Explaining Spinal Anesthesia to Pregnant Women: A Visual Approach to Overcoming Fears

Primary outcome: To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog.

Secondary outcomes: To analyze independent (age, education, profession, previous experiences) and dependent (fear, anxiety) factors influencing patient choices.

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

318

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: ilke dolgun

Study Locations

  • Turkey
    • Merkez Mahallesi
      • Istanbul, Merkez Mahallesi, Turkey, 34250

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

The study will include 318 pregnant women aged 18-45 who are undergoing elective cesarean sections and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale.

Description

Inclusion Criteria:

  • Aged 18-45
  • who are undergoing elective cesarean sections
  • and classified as ASA I-II according to the American Society of Anesthesiologists (ASA) scale

Exclusion Criteria:

  • patients under 18 or over 45 years old,
  • emergency cesareans,
  • preeclampsia,
  • cardiovascular disorders,
  • fetal abnormalities,
  • those not receiving spinal anesthesia or converted to general anesthesia during surgery,
  • those who refuse to participate in the study,
  • hospital clinical or administrative staff,
  • patients with psychiatric disorders

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
incidence of spinal anesthesia preference
Time Frame: 4 MONTH
To determine the incidence of spinal anesthesia preference after exposure to the visual information catalog
4 MONTH

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Istinye University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

April 1, 2025

Primary Completion (Estimated)

August 1, 2025

Study Completion (Estimated)

August 15, 2025

Study Registration Dates

First Submitted

March 28, 2025

First Submitted That Met QC Criteria

March 28, 2025

First Posted (Actual)

April 4, 2025

Study Record Updates

Last Update Posted (Actual)

April 4, 2025

Last Update Submitted That Met QC Criteria

March 28, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • haseki broşür

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Incidence of Spinal Anesthesia Preference

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Denmark

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe