- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05660551
Investigation of the Effect of Different Training Techniques in Teaching the Management of Shoulder Dystocia
Effect of Different Training Techniques in Teaching the Management of Shoulder Dystocia
In this study, it was aimed to determine the effect of demonstration, telesimulation and game-based teaching on teaching shoulder dystocia management in midwifery students.
H01: There is no difference between the four groups in terms of satisfaction with learning.
H02: There is no difference between the four groups in terms of Self-Confidence in Learning.
H03: There is no difference between the four groups in terms of Motivation scores in Teaching Materials.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey, 06620
- Ankara University Faculty of Nursing
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Being a registered student in the midwifery department,
- Having the ability to manage normal birth,
- Having a smart phone, tablet or computer with internet connection,
- Agreeing to participate in the research
Exclusion Criteria:
- to suspend education.
- Having received formal training on shoulder dystocia management.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control Group
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Experimental: Demonstration group
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This group will be demonstrated on a model after the theoretical training.
The maneuvers used in the management of shoulder dystocia will be shown to the students on the model, respectively.
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Experimental: Telesimulation Group
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After the theoretical training for this group, telesimulation will be applied.
A scenario will be created for the telesimulation experience and a video will be shot with this scenario.
These videos will be watched by the students in groups of 4 on Microsoft Teams and a case discussion will be made through this scenario.
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Experimental: Kahoot Game Group
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Kahoot, a game-based program, will be applied to this group one week after the theoretical training.
The game will be organized according to the learning objectives and achievements related to shoulder dystocia.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Shoulder Dystocia Skill Checklist
Time Frame: 15 days after the training
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The skill checklist prepared by the researcher by scanning the literature consists of three parts (Taşkın, 2016; Sayıner & Başkaya, 2020); diagnosing shoulder dystocia, making the necessary interventions for shoulder dystocia at birth, and intervention after birth.In the skill list, the student will receive 1 point for each correct application, and 0 points for each incorrect or skipped application.Higher scores indicate higher skill levels.
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15 days after the training
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Instructional Materials Motivation Survey
Time Frame: 15 days after the training
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The Instructional Materials Motivation Survey (IMMS) aims to assess the motivational characteristics of instructional materials or courses using the Attention, Relevance, Confidence, and Satisfaction (ARCS) model of motivation. The five-point Likert type scale consists of 36 items in the original scale. In the last Turkish adaptation study, 3 of the items were excluded from the original scale and a total of 33 items were included in the Turkish version of the scale. |
15 days after the training
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Change in Self-Sufficiency
Time Frame: immediately before the training, immediately after the training
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Visual Analog Scale (VAS)- assessed by adequate vision.
For each item, students rated their sense of self-sufficiency on a scale of 0 (very inadequate) to 10 (very adequate).
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immediately before the training, immediately after the training
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 737219
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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