Scenario-Based Simulation

NCT ID: NCT06870227

Last Updated: 2025-03-11

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-04-01
• Study Completion Date: 2025-06-01

Brief Summary

The aim of this study is to determine the effect of Scenario-Based Simulation on Clinical Learning, Confidence and Satisfaction of Midwifery Students in Management of Eclampsia Crisis in Labor

Detailed Description

Hypotheses 01; there was no difference between the clinical learning score of the experimental group and the pain score of the control group.

H02; there was no difference between the confidence score of the experimental group and the confidence score of the control group.

H03; there was no difference between the satisfaction score of the of the experimental group and the satisfaction score of the control group.

The study will be carried out in two different groups. The practice will start with meeting the students. After the students are evaluated in terms of eligibility criteria for the research, the students who are eligible will be informed about the research and written informed consent will be obtained from the students who accept. The random distribution of students to the study groups will be carried out using the Block Randomization method. The following applications will be made to the groups.

Eclampsia Crisis in Labor training will be given by the responsible investigator, and then one of the groups separated by randomization will perform Eclampsia Crisis in Labor first care on the second group model using High Reality Simulator. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one

Conditions

Simulation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: SINGLE

Study Groups

High Reality Simulator

Eclampsia Crisis in Labor management training will be given by the responsible investigator, and then one of the groups will be allocated by randomization. Using High Reality Simulator will perform emergency Eclampsia Crisis in Labor. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.

Group Type: EXPERIMENTAL

Using High Reality Simulator

Intervention Type: OTHER

Using High Reality Simulator will perform emergency eclampsia in labour

control group

Using model will perform emergency y Eclampsia Crisis in Labor. These trainings will first be in the form of the instructor responsible for the groups demonstrating the application, and then the students will apply it one by one.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Using High Reality Simulator

Using High Reality Simulator will perform emergency eclampsia in labour

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Volunteer to participate in the study
• Take the Obstetric Emergencies course

Exclusion Criteria

• Not volunteering to participate in the study
• Not taking the obstetric emergencies course

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Ondokuz Mayıs University

OTHER

Sponsor Role: lead

Responsible Party

Sümeyye BAL

Ph.D.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Ondokuz Mayis University

Samsun, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

2024/572

Identifier Type: -

Identifier Source: org_study_id