NCT07530692

Brief Summary

This study aims to evaluate the effect of a video-supported flipped learning model on anxiety and skill levels of midwifery students in episiotomy education. Episiotomy is an important clinical skill in midwifery education, and the method used to teach this skill may influence students' anxiety and performance. This randomized controlled educational study will be conducted with midwifery students who are enrolled in the episiotomy course. Participants will be randomly assigned to either an intervention group or a control group. Students in the intervention group will receive episiotomy education using a video-supported flipped learning model, in which theoretical content is provided through instructional videos prior to in-class activities. The control group will receive traditional classroom-based education. Students' anxiety levels and episiotomy skill performance will be assessed using validated measurement tools before and after the educational intervention. The findings of this study are expected to contribute to evidence-based teaching strategies in midwifery education and support the use of innovative learning models to improve student outcomes.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable anxiety

Timeline
1mo left

Started Apr 2026

Shorter than P25 for not_applicable anxiety

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress64%
Apr 2026Jul 2026

First Submitted

Initial submission to the registry

January 18, 2026

Completed
3 months until next milestone

First Posted

Study publicly available on registry

April 15, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

April 15, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 20, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2026

Expected
Last Updated

April 15, 2026

Status Verified

March 1, 2026

Enrollment Period

1 month

First QC Date

January 18, 2026

Last Update Submit

April 8, 2026

Conditions

Keywords

EpisiotomyVideo-Based LearningMidwifery StudentsSimulation TrainingRandomized Controlled Trial

Outcome Measures

Primary Outcomes (2)

  • State Anxiety Level

    State (situational) anxiety will be assessed using the State subscale of the State-Trait Anxiety Inventory (STAI) to determine students' momentary anxiety related to episiotomy skills training. Higher scores indicate higher state anxiety.

    Immediately before and immediately after the training session, up to 1 day

  • Episiotomy Skill Performance Score

    Episiotomy skill performance will be evaluated using the Episiotomy Skill Assessment Form (ESAF), a 40-step procedure scored from 0 to 100, where higher scores indicate higher skill performance.

    Immediately after completion of the training session, up to 1 da

Study Arms (2)

Video-Supported Flipped Learning Episiotomy Education

EXPERIMENTAL

Participants in this arm will receive episiotomy education using a video-supported flipped learning model. Theoretical content will be provided through instructional videos before face-to-face sessions, followed by interactive discussions and supervised skills practice in the skills laboratory.

Behavioral: Video-Supported Flipped Learning Model

Control

NO INTERVENTION

Traditional Classroom-Based Episiotomy Education

Interventions

An educational intervention in which episiotomy-related theoretical content is delivered through instructional videos prior to classroom sessions, with in-class time dedicated to interactive learning and supervised skills practice.

Video-Supported Flipped Learning Episiotomy Education

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Midwifery 3rd-year student who is taking the Normal Birth course
  • Willing to participate and provides informed consent
  • Has not received prior education in the health field during associate or undergraduate education
  • Has access to the internet and has a computer and/or smartphone

You may not qualify if:

  • Incomplete completion of data collection forms
  • Has received prior education in the health field during associate or undergraduate education
  • No access to the internet, computer, or smartphone
  • Does not participate in the study procedures/intervention sessions
  • Requests to withdraw from the study at any time

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Anxiety Disorders

Condition Hierarchy (Ancestors)

Mental Disorders

Central Study Contacts

Reyhan Aydin Dogan, Associate Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to one of two parallel groups: an intervention group receiving video-supported flipped learning-based episiotomy education and a control group receiving traditional classroom-based education. Each participant will be assigned to a single study arm and will receive only the educational approach allocated to that arm throughout the study.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
ASSOCIATE PROFESSOR

Study Record Dates

First Submitted

January 18, 2026

First Posted

April 15, 2026

Study Start

April 15, 2026

Primary Completion

May 20, 2026

Study Completion (Estimated)

July 20, 2026

Last Updated

April 15, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared because the study involves student-level educational and psychological data collected within a single-center academic research project. Data confidentiality and participant privacy will be protected in accordance with ethical approval and institutional policies. Only de-identified, aggregated results will be reported and made publicly available.