The Effect of Virtual Reality Application in Cervical Dilatation and Effacement Teaching
1 other identifier
interventional
102
0 countries
N/A
Brief Summary
The aim of this project is to determine the effect of virtual reality application in cervical dilatation and effacement teaching on students' satisfaction, confidence and anxiety levels.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2023
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
July 12, 2023
CompletedFirst Posted
Study publicly available on registry
August 8, 2023
CompletedStudy Start
First participant enrolled
September 15, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 15, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 20, 2023
CompletedAugust 8, 2023
August 1, 2023
1 month
July 12, 2023
August 1, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Descriptive Information Form
It consists of nine questions questioning students' socio-demographic characteristics, knowledge of cervical dilatation and effacement, and their virtual reality application experiences.
5 minutes before the study
Secondary Outcomes (1)
Student Satisfaction and Self-Confidence in Learning Scale
5 minutes after the study
Other Outcomes (1)
State and Trait Anxiety Inventory
30 minutes after study
Study Arms (2)
virtual reality group
EXPERIMENTALAfter the introduction and information is given, the lens and pupil distances of the virtual reality glasses will be adjusted according to each student and the students will be provided to wear them. The application will be made one-on-one with each student. The application will be carried out sitting in the laboratory. While the students are inside the application, the interface will be introduced through the images projected to the computer simultaneously. Cervical dilatation and effacement application will be watched using virtual glasses. Then, the students will be asked to use their hands to touch the perineum of the woman and make the image transparent, and it will be ensured that they watch the cervix structures again. Each student will use the virtual glasses for an average of 20-25 minutes.
Model group
NO INTERVENTIONAfter the introduction and briefing, the students will be provided to perform cervical dilatation and effacement application on the model in accordance with the Cervical Dilatation and Effacement Learning Guide with each student in the laboratory environment.
Interventions
Before the training, the Descriptive Information Form and the State and Trait Anxiety Inventory as a pre-test will be applied by face interview method. They will study for two hours. After the introduction and information, the lens and pupil distances of the virtual reality Glasses will be adjusted according to each student and students are expected to wear their vision. The application is the same for every student. Students will be introduced through the images projected to the computer simultaneously while in the application. Cervical dilation and effacement application will be monitored using virtual reality glasses. Next, the students will be asked to touch the woman's perineum with their hands to make her image transparent and we ask them to watch the cervix structures again. After the application, "Learning Satisfaction and Self-Confidence in Learning Scale" and "State and Trait Anxiety Inventory" will be applied as a post-test.
Eligibility Criteria
You may qualify if:
- Being a third year student of the Midwifery Department,
- Not having received training in cervical dilation and effacement application
- Volunteering to participate in the study
You may not qualify if:
- Not voluntarily participating in the study,
- Having received training in cervical dilatation and effacement
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sevgi Beyazgüllead
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- midwife
Study Record Dates
First Submitted
July 12, 2023
First Posted
August 8, 2023
Study Start
September 15, 2023
Primary Completion
October 15, 2023
Study Completion
December 20, 2023
Last Updated
August 8, 2023
Record last verified: 2023-08