NCT06724003

Brief Summary

The aim of this study was to evaluate the effect of computer-based virtual reality (VR) simulation on students' knowledge, satisfaction and self-confidence in teaching oral care practice in the unconscious patient. Oral care practice in the unconscious patient is one of the important nursing interventions in terms of patient health, which is given from the first years of nursing education. This study is a randomized controlled experimental research. The study will be conducted with first-year nursing students enrolled in a university in Turkey. The sample of the study will consist of 68 nursing students. The data will be collected by Student Information Form, Oral Care Practice Information Form, Student Satisfaction in Learning and Self-Confidence Scale.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
68

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

November 25, 2024

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

November 26, 2024

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 9, 2024

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 25, 2025

Completed
2 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 27, 2025

Completed
Last Updated

September 4, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

November 26, 2024

Last Update Submit

August 28, 2025

Conditions

Keywords

virtual realitynursing studentconfidencesatisfactionsimulation

Outcome Measures

Primary Outcomes (1)

  • Student Satisfaction and Self-confidence in Learning Scale (SCLS)

    The scale developed by Jeffries \& Rizzolo consists of 13 items. The Turkish validity and reliability study of the scale was conducted by Ünver et al. In this form, the number of items was reduced to 12. There are 5 items in the "Satisfaction with Current Learning" subscale and 7 items in the "Confidence in Learning" subscale. The Cronbach alpha value in the Turkish version is 0.85 for satisfaction with learning and 0.77 for self-confidence in learning. The scale is a 5-point Likert scale; responses are measured with values between 1 (strongly disagree) and 5 (strongly agree). Scale scores are obtained by dividing the sum of the sub-dimensions by the number of items. Accordingly, the minimum score is 1 and the maximum score is 5. It is thought that the higher the score obtained from the scale, the higher the satisfaction and self-confidence.

    two weeks

Secondary Outcomes (2)

  • Student Information Form

    two weeks

  • Oral Care Practice Information Form

    two weeks

Study Arms (2)

Computer-based simulation of virtual reality .

EXPERIMENTAL

Interactive virtual reality simulation group will practice oral care in the unconscious patient with interactive virtual reality simulation after the oral care practice in the unconscious patient is demonstrated on a low reality patient manikin. After the application, a briefing will be given to the participants and the application will be discussed in detail. Participants will perform oral care in the unconscious patient on a low-reality patient manikin 15 days after the simulation application.

Other: Computer-based virtual reality simulation

Low-reality patient model group

NO INTERVENTION

Participants will be demonstrated the unconscious patient oral care practice with a low-reality patient manikin by the researcher nurse faculty member. Participants will perform the application on the low-reality patient manikin. After the application, participants will be briefed and talked about the application. Oral care of the unconscious patient will be practiced on a low-reality patient manikin 15 days after the application.

Interventions

The computer-based virtual practice simulation was created as a single scenario for oral care practice in the unconscious patient. The scenario software was created and designed by the researcher who is an IT specialist. In the formation phase of the scenario, the software was realized by working together with the researcher, the expert faculty member, the nurse and the informatics specialist for the photographs required for the virtual reality application and the steps of the scenario software.

Also known as: Experimental group
Computer-based simulation of virtual reality .

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Basic Principles and Concepts in Nursing course for the first time,
  • Volunteering to participate in the study.

You may not qualify if:

  • Graduating from a health-related high school or an associate's or bachelor's degree from a health-related university,
  • Having received training on oral care practice in the unconscious patient.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Giresun University Faculty of Health Sciences

Giresun, Piraziz, 28340, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Personal Satisfaction

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Asuman Çobanoğlu Assistant Professor, PhD.

    Giresun University Faculty of Health Sciences

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Statistical analyses and data reporting of the study will be carried out by statistical experts who are not among the researchers and are not familiar with the research application. The study was blinded in terms of outcome measures, statistical analysis and reporting to prevent statistical and reporting bias. In this context, the statistical expert was blinded; the researchers and students were not blinded.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This study is a randomized controlled experimental trial.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

November 26, 2024

First Posted

December 9, 2024

Study Start

November 25, 2024

Primary Completion

February 25, 2025

Study Completion

February 27, 2025

Last Updated

September 4, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

It will be shared when requested from the researcher.

Locations