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Nursing StudentNCT06724003

The Effect of Simulation on Nursing Education

A study testing Computer-based virtual reality simulation in people with Nursing Student, run by Giresun University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Nursing Student
What is being tested?
Computer-based virtual reality simulation
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
68 participants
Where
1 siteTurkey (Türkiye)
Study dates
25 Nov 2024to 27 Feb 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Giresun University Faculty of Health Sciences

    Giresun, Piraziz, 28340

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Computer-based Virtual Reality Simulation on Nursing Students' Knowledge, Self-confidence and Satisfaction Levels: Oral Care Practice in Unconscious Patient

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.

Read the detailed description

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 practices 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. Participants will be randomized into a computer-based virtual reality simulation group (n=34) and a low-reality patient manikin group (n=34). The research data will be collected by Student Information Form, Oral Care Practice Information Form, Student Satisfaction in Learning and Self-Confidence Scale.

Participants in the experimental and control groups will be informed about the methodology, aims and objectives of the study and their consent to participate in the study will be obtained both verbally and in writing. The theoretical content of the course will be given to the participants by the researcher faculty member using power point presentation and question-answer method. After the theoretical training, students will fill in the Student Information Form and Oral Care Practice Information Form.

After the forms are filled in, the students in both groups will be taken to the laboratory where the low-reality patient model is located. Students will be given a checklist showing the steps of oral care practice in the unconscious patient before the application. Oral care application steps in the unconscious patient will be shown to the students on the low-reality patient model by the researcher nurse faculty member. The participants in the control group will perform the oral care skill in the unconscious patient on the model.

The participants in the experimental group will then be taken by the researchers to the laboratory where the computer-based interactive VR simulation is used. Participants will be given a checklist showing the oral care application steps in the unconscious patient before the simulation application. Participants will be given preliminary information about the computer-based interactive VR simulation system and its application. Oral care practice in the unconscious patient will be demonstrated to the participants in the interactive VR simulation by the research nurse faculty member. Participants will be allowed to ask questions during the simulation and their questions will be answered. After the hands-on training, the participants will be taken to the laboratory one by one to practice oral care in the unconscious patient with the interactive VR simulation. While the participant is practicing oral care in the unconscious patient in the simulation application, the researcher faculty member will control the oral care practice of the participants. While the participant is practicing oral care in the unconscious patient in the simulation application, the researcher faculty member will check the skill steps on the participants' oral care practice checklist.

After a participant finishes the practice and leaves the laboratory, another participant will be called to the room for the practice and each participant will be given an average of 10 minutes for the practice. After the application is completed, each participant will fill in the Oral Care Application Information Form and the Student Satisfaction and Confidence in Learning Scale. After the implementation process, information sessions will be held with the participants in the experimental and control groups. These sessions will be held with groups of 5-6 students. Reassuring and open communication was established with the participants and they were encouraged to think. In the debriefing session, the participants will be asked "What did you do well?" and "What would you do differently if you had the opportunity to experience this simulation again?" and will be asked to give reflective answers. Participants will be given feedback about their performance by the trainer in line with the skill checklists used. Participants in the experimental and cortol groups will be asked to practice oral care in the unconscious patient in the simulation and low-reality patient mannequin 15 days after the oral care practice in the low-reality patient mannequin in the unconscious patient. Participants will fill in the Oral Care Practice Information Form and the Student Satisfaction and Self-confidence in Learning Scale after completing the practices.

Conditions
Nursing Student
Being tested
Computer-based virtual reality simulation
Keywords
virtual reality, nursing student, confidence, satisfaction, simulation
Medical subject headings
Personal Satisfaction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Computer-based virtual reality simulationOther

    Also called Experimental group

    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.

Study groups in NCT06724003
Study groupRoleWhat they receive
Computer-based simulation of virtual reality .ExperimentalInteractive 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.
Receives: Other: Computer-based virtual reality simulation
Low-reality patient model groupNo interventionParticipants 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.

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: two weeks

Secondary outcomes (2)
  1. Student Information Form

    It was prepared by the researchers based on previous studies in the literature. The form consists of 9 questions inquiring the demographic and academic information and technology usage characteristics of the participating students (gender, year of birth, academic average, computer use, etc.).

    Measured: two weeks

  2. Oral Care Practice Information Form

    This form was developed by the researchers by reviewing the relevant literature in accordance with the oral care application steps in unconscious patients. After the relevant form was developed by the nurse faculty member, it was also examined and edited by 2 nurse faculty members who are experts in the field. The form includes 18 items for oral care practice in unconscious patients. The statements in the form consist of 3 options as true, false and don't know/no idea. In the form, the "Correct" response of the students to the statements corresponds to 1 point, and "Incorrect" or "Don't Know/No Idea" responses correspond to 0 points. Students can get a maximum of 18 points and a minimum of 0 points from this form.

    Measured: two weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Dec 2024
  2. Study start25 Nov 2024
  3. Primary completion25 Feb 2025
  4. Study completion27 Feb 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
This study is a randomized controlled experimental trial.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
68 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06724003
Sponsor's protocol ID
GiresunU-SBF-AC-01
Status last verified
Aug 2025
First submitted
26 Nov 2024
Last updated
4 Sep 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: It will be shared when requested from the researcher.

Questions about this trial

What is this clinical trial studying?

A study testing Computer-based virtual reality simulation in people with Nursing Student, run by Giresun University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Student Satisfaction and Self-confidence in Learning Scale (SCLS) (time frame: two weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Sep 2025.

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