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Teaching Fetal Development With Virtual Reality

NCT04444258 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2021-10-01

No results posted yet for this study

Summary

In this study, it was aimed to design virtual pregnancy for pregnancy formation, fetal and placental development in the virtual reality environment and to evaluate the effectiveness of the designed virtual pregnancy on midwifery education.

Our study, which will be the first in our second country in the world, aims to reduce the application errors and determine deviations from normal by examining the formation of pregnancy, maternal, fetal and placental changes, which form the basis of midwifery profession, before having clinical experience. In this direction, the objectives of our study are;

* Development of the virtual pregnancy application, which will be designed for the first time in our country,
* Ensuring the effective use of virtual pregnancy practice in midwifery education,
* Visualizing fetal and placental development with virtual pregnancy that will form the basis of midwifery education,
* To minimize the application errors experienced in clinical practices of midwifery students,
* To increase educational effectiveness, clinical and academic success by visualizing the formation of pregnancy.
* Measuring cognitive loadings of students after education
* Measuring students' sense of readiness

Conditions

  • Educational Problems

Interventions

OTHER

Application of computer aided virtual reality glasses

Experimental I Group: After the Fetal Development Assessment Information Form (FEGBF), a computer-aided and guided virtual reality application prepared by the researchers including the phases of the fetus week by week will be watched and then FEGBF will be applied again by changing the locations of the questions.

OTHER

Teaching fetal development theoretically

Control Group: FEGBF will be applied after 4 hours of theory training. Virtual pregnancy application will not be watched.

Sponsors & Collaborators

  • Saglik Bilimleri Universitesi

    collaborator OTHER

  • Karabuk University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
24 Months
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-03-15
Primary Completion
2021-07-15
Completion
2021-09-10

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04444258 on ClinicalTrials.gov