Evaluation of the Effectiveness of Teaching Method With Simulation in Electronic Fetal Monitoring Management

NCT ID: NCT05904314

Last Updated: 2025-04-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-15

Study Completion Date

2025-04-10

Brief Summary

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Electro fetal monitor monitoring in the antepartum and intrapartum periods is one of the most important responsibilities of midwives, who have important roles and responsibilities in maintaining and managing the health of women and newborns before, during and after delivery. Although midwives receive training on EFM monitoring with classical methods before graduation, they may experience problems in EFM monitoring in the clinical field after graduation. For this reason, midwife students should have the knowledge, skills and self-efficacy about a good level of EFM monitoring during their undergraduate education. In recent years, simulation-based education in the field of health has increased rapidly. This method creates an opportunity for health professionals, students, patient assessment, interaction and holistic care without compromising patient safety, and develops participants' critical thinking, clinical decision making and problem solving skills.

In this context, it is very important to evaluate the EFM trace in the antepartum and intrapartum periods, to determine the possible risks, to plan, implement and evaluate the interventions, to provide the emergency crisis management in a short time without affecting the fetal health, and to increase the self-confidence of the midwives.

The research was planned quantitatively in the form of randomized control-intervention of the scenario-based realistic simulation method, to increase the satisfaction and self-confidence levels of midwifery students in learning, to evaluate the simulation design and educational effectiveness, in EFM management. The research will facilitate midwifery students to intervene with the patient in a shorter time, with confidence and with sufficient clinical skills, and patient safety will be increased. It will also allow for the reduction of erroneous clinical practices and malpractices.

This research aims to evaluate the effect of high-fidelity simulation teaching method on knowledge, satisfaction and self-efficacy of midwifery students in EFM follow-up.

Detailed Description

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Conditions

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Cardiotocography Electronic Fetal Monitoring High Fidelity Simulation Training

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

68 participants, control group theory training experimental group Electronic fetal monitor management simulation
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Experimental Group

Investigation of the effectiveness of scenario-based standardized patient simulation training and electronic fetal monitor management of midwifery students

Group Type EXPERIMENTAL

Simulation training in electronic fetal monitor management

Intervention Type BEHAVIORAL

Simulation training in electronic fetal monitor management

Control Group

Behavioral: Examining the effectiveness of electronic fetal monitor management of midwifery students with theory training

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Simulation training in electronic fetal monitor management

Simulation training in electronic fetal monitor management

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Agreeing to participate in the research,
* Being a midwifery second year student and taking the "Risky pregnancy" course,
* Attending training with simulation for the first time

Exclusion Criteria

* Incomplete filling of data collection forms,
* Not participating in all applications of simulation teaching,
* Desire to leave the research.
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Saglik Bilimleri Universitesi

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Iffet Güler Kaya

Fatih, Istanbul, Turkey (Türkiye)

Site Status RECRUITING

Neriman

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Facility Contacts

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iffet G kaya

Role: primary

05064223056

Neriman Zengin

Role: primary

05064223056

Role: backup

05064223056

Other Identifiers

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IGULER

Identifier Type: -

Identifier Source: org_study_id

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