NCT05982457

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

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
102

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Status
unknown

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

Completed
27 days until next milestone

First Posted

Study publicly available on registry

August 8, 2023

Completed
1 month until next milestone

Study Start

First participant enrolled

September 15, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2023

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 20, 2023

Completed
Last Updated

August 8, 2023

Status Verified

August 1, 2023

Enrollment Period

1 month

First QC Date

July 12, 2023

Last Update Submit

August 1, 2023

Conditions

Keywords

cervical dilationmidwifery educationsimulationvirtual reality

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

EXPERIMENTAL

After 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.

Behavioral: virtual reality group

Model group

NO INTERVENTION

After 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.

virtual reality group

Eligibility Criteria

Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

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