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Mixed Reality Training for Teaching Cervical Effacement and Dilation

M

Mardin Artuklu University

Status

Enrolling

Conditions

Labor; Poor, Primary

Treatments

Other: Standard Education Group
Other: mixed reality education

Study type

Interventional

Funder types

Other

Identifiers

NCT07238205
MAU-Midwifery-UG-01

Details and patient eligibility

About

The aim of this educational research is to determine whether a mixed reality-based training program is effective in teaching midwifery students how to assess cervical effacement and dilation. The study also examines the impact of mixed reality on students' cognitive load, sense of presence, and midwifery professional perception.

The main questions the study seeks to answer are:

Does mixed reality training reduce students' cognitive load?

Does mixed reality increase the students' sense of presence?

How does mixed reality-based training influence students' professional perception of midwifery?

Do students who receive mixed reality training perform better in assessing cervical effacement and dilation on real pregnant women compared with the control group?

Full description

The aim of this educational research is to determine whether a mixed reality-based training program is effective in teaching midwifery students how to assess cervical effacement and dilation. The study also examines the impact of mixed reality on students' cognitive load, sense of presence, and midwifery professional perception.

The main questions the study seeks to answer are:

Does mixed reality training reduce students' cognitive load?

Does mixed reality increase the students' sense of presence?

How does mixed reality-based training influence students' professional perception of midwifery?

Do students who receive mixed reality training perform better in assessing cervical effacement and dilation on real pregnant women compared with the control group?

How the research will be conducted:

Researchers will compare a mixed reality intervention group with a control group receiving traditional training. Students in both groups will evaluate five different pregnant women to assess cervical effacement and dilation in real clinical settings.

Participants will:

Receive either mixed reality-based training (intervention) or traditional instruction (control)

Complete the Cognitive Load Scale, Sense of Presence Scale, and Midwifery Professional Perception Scale

Perform cervical effacement and dilation assessments on five pregnant women during clinical practice

Enrollment

90 estimated patients

Sex

Female

Ages

18 months to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Enrolled in the Midwifery Department at Mardin Artuklu University,
  • Taking the course "Normal Birth and Postpartum Care,"
  • Who have not previously received any structured training (practical training, simulation, etc.) related to vaginal examination or cervical dilation/effacement procedures,
  • Who do not feel confident in assessing cervical effacement and dilation,
  • Who volunteer to participate in the study will be included,
  • Pregnant women who are in the first stage of labor and have no obstetric complications.

Exclusion criteria

  • Individuals who are graduates of health vocational high schools,
  • Have disabilities in their eyes, hands, arms, or fingers,
  • Those who do not complete the training will not be included.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 2 patient groups

Mixed Reality Training Group
Experimental group
Description:
Students will participate in a mixed reality (MR)-based training program.
Treatment:
Other: mixed reality education
Standard Education Group
Active Comparator group
Description:
Students in the control group will receive traditional theoretical instruction.
Treatment:
Other: Standard Education Group

Trial contacts and locations

1

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Central trial contact

Ülkin Gündüz Aruser, Ph.D; Hacer Ünver Koca, Assoc. Prof.

Data sourced from clinicaltrials.gov

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