Management of Shoulder Dystocia in Flipped Learning

July 24, 2025 updated by: Reyhan Aydin Doğan, Karabuk University

The Effect of a Flipped Learning Approach on Midwifery Students Learning Shoulder Dystocia Management: A Randomized Controlled Trial.

Flipped learning is an innovative learning method in midwifery education. Studies that apply this learning method together with shoulder dystocia training have not been found in the current literature. For this reason, the study was designed as a randomized controlled study to examine the effectiveness of the flipped learning technique in shoulder dystocia management using high-valid simulation in midwifery undergraduate education.

Study Overview

Status

Completed

Detailed Description

Flipped learning is an innovative learning method in midwifery education. Studies that apply this learning method together with shoulder dystocia training have not been found in the current literature. For this reason, the study was designed as a randomized controlled study to examine the effectiveness of the flipped learning technique in shoulder dystocia management using high-valid simulation in midwifery undergraduate education.

Hypotheses of the research;

First Hypothesis H1: The use of flipped learning model in midwifery education has an effect on midwifery students' shoulder dystocia knowledge levels.

Second Hypothesis H1: The use of flipped learning model in midwifery education has an effect on midwifery students' levels of Student Satisfaction and Self-Confidence in Learning.

Third Hypothesis H1: The use of flipped learning model in midwifery education has an effect on midwifery students' Pagana Clinical Stress levels.

Study Type

Interventional

Enrollment (Actual)

68

Phase

  • Not Applicable

Contacts and Locations

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

Study Locations

      • Karabuk, Turkey, 78500
        • Reyhan Aydin Doğan

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

Yes

Description

Inclusion Criteria:

  • - Agreeing to participate in the study,
  • Being a 4th year student at the Department of Midwifery,

Exclusion Criteria:

  • - Refusing to participate in the study,
  • Being a 1st, 2nd and 3rd year student in the midwifery department

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

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: flipped learning group
In addition to the traditional theory training to be given within the scope of the study, two hours of video-supported shoulder dystocia training will be given using the university's corporate Microsoft teams program, one day before the simulation application. The videos used in the training consist of previously shot training videos. There is no copyright or legal problem in using the videos.
flipped learning training group. Applying a flipped learning model in addition to routine training in a fully equipped simulation
No Intervention: routine training group- control group
The control group will be given shoulder dystocia theory training before the simulation training within the routine course protocol within the scope of the routine risky birth and postpartum period course.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
H1
Time Frame: 12 months
Using the flipped learning model in midwifery education increases the knowledge level score of midwifery students on shoulder dystocia.
12 months
H1
Time Frame: 12 months
Using the flipped learning model in midwifery education reduces the PANAGA clinical stress level score of midwifery students.
12 months
H1
Time Frame: 12 months
Using the flipped learning model in midwifery education increases midwifery students' oStudent Satisfaction and Self-Confidence in Learning Scale scores.
12 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Measurement and evaluation materials to be used in the study
Time Frame: Scales will be administered immediately after the educational intervention.
In the study, a personal data form containing students' personal information,
Scales will be administered immediately after the educational intervention.
Measurement and evaluation materials to be used in the study
Time Frame: Scales will be administered immediately after the educational intervention.
Shoulder Dystocia and Management Information Form
Scales will be administered immediately after the educational intervention.
Measurement and evaluation materials to be used in the study
Time Frame: Scales will be administered immediately after the educational intervention.
Shoulder Dystocia Management Individual Evaluation Form will be used to determine the effectiveness of the training.
Scales will be administered immediately after the educational intervention.
Measurement and evaluation materials to be used in the study
Time Frame: Scales will be administered immediately after the educational intervention.
The Student Satisfaction and Self-Confidence Scale in Learning will be used to determine students' simulation competencies and satisfaction,
Scales will be administered immediately after the educational intervention.
Measurement and evaluation materials to be used in the study
Time Frame: Scales will be administered immediately after the educational intervention.
The Pagana Clinical Stress Survey will be used to determine the stress caused by application techniques on students.
Scales will be administered immediately after the educational intervention.

Collaborators and Investigators

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

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.

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 (Actual)

June 6, 2024

Primary Completion (Actual)

June 10, 2024

Study Completion (Actual)

June 30, 2025

Study Registration Dates

First Submitted

October 16, 2023

First Submitted That Met QC Criteria

October 23, 2023

First Posted (Actual)

October 27, 2023

Study Record Updates

Last Update Posted (Actual)

July 28, 2025

Last Update Submitted That Met QC Criteria

July 24, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

It will be shared when the work is completed.

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.

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