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RecruitingNCT07663851VRUpdated Jun 23, 2026

EFFECTIVENESS OF VIRTUAL REALITY SIMULATION

An interventional study of Virtual Reality Simulation in Clinical Decision Making, sponsored by Istanbul Arel University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 23 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-23.

Sponsored by Istanbul Arel University · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jun 2026, 4 months ago, but the record still lists the study as recruiting.
  • Started Mar 2026; still recruiting 8 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
18 Years to 23 Years
Sex
All
01

Study summary

This randomized controlled trial aims to evaluate the effects of VRS on decision-making skills, self-confidence levels, and anxiety of psychiatric nursing students. Students participating in the study will be divided into two groups: intervention and control groups. VRS, which includes a scenario of a patient with schizophrenia, will be applied to the intervention group at the beginning of the academic term, before students start clinical practice, and in the middle of the term. The control group will be subjected to theoretical courses and clinical practice. Data will be collected using the Clinical Decision-Making, Self-Confidence, and Anxiety Scale, Personal Information Form, and Modified Simulation Effectiveness Tool. Measurements will be performed at three time points: before the simulation, in the middle of the academic term, and at the end of the academic term. In addition, debriefing sessions will be held with students participating in VRS in groups of 4-5 within the scope of the simulation process. It is expected that the findings obtained as a result of the study will make significant contributions to the literature in understanding the effects of VRS on psychiatric nursing education. At the same time, this study aims to demonstrate that this VRS, designed specifically for the Turkish language and culture, can be an effective tool to increase the self-confidence levels of psychiatric nursing students in their clinical decision-making processes and to reduce their anxiety levels within the scope of the psychiatric nursing course. The results of the study are intended to guide the development of new approaches to the use of technology in psychiatric nursing education and the integration of technology-based VRS into the psychiatric nursing curriculum.

Read the detailed description

This randomized controlled trial aims to investigate the impact of a schizophrenia-focused virtual reality simulation (VRS) on clinical decision-making skills. This randomized controlled trial aims to investigate the impact of a schizophrenia-focused virtual reality simulation (VRS) on clinical decision-making skills, self-confidence, and anxiety levels of undergraduate psychiatric nursing students. The study will be conducted with second- or third-year nursing students enrolled in a psychiatric nursing course at a university in Türkiye.

Participants will be randomly assigned to either the intervention or control group. The intervention group will participate in VRS, which includes an interactive, gamified simulation scenario based on a patient diagnosed with schizophrenia. This simulation will be conducted twice: once at the beginning of the academic term, prior to clinical placement, and again at mid-term. Each simulation session will be followed by structured debriefing sessions held in small groups (4-5 students), led by a trained facilitator to enhance reflective learning and reinforce clinical reasoning.

The control group will receive standard psychiatric nursing education, consisting of theoretical lectures and routine clinical practice, without exposure to VRS.

Data will be collected using the Clinical Decision-Making Scale, Self-Confidence Scale, Anxiety Scale, Personal Information Form, and the Modified Simulation Effectiveness Tool (SET-M). Measurements will be taken at three time points: (1) before the first VRS session or clinical practice, (2) at mid-term, and (3) at the end of the academic term.

This study is expected to contribute significantly to the understanding of how technology-enhanced, culturally tailored simulation tools affect learning outcomes in psychiatric nursing education. Specifically, it aims to demonstrate that VRS can enhance students' self-confidence in clinical decision-making and reduce their anxiety before and during psychiatric clinical placements. The findings are anticipated to guide the future integration of digital simulation technologies into psychiatric nursing curricula in Türkiye and globally.

02

Conditions studied

  • Clinical Decision Making

Keywords

  • virtual reality
  • simulation
  • clinical decision making
  • mental health nursing
  • students
03

In context

Lead sponsor

Istanbul Arel University is the lead sponsor of 44 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 23 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • To be registered for the Psychiatric Nursing course in the 2024-2025 spring semester,
  • To be taking the Psychiatric Nursing course for the first time,
  • To attend the course regularly,
  • Not to have received any training with virtual reality simulation within the scope of the Psychiatric Nursing course before,
  • Not to have practiced in a Mental Health and Diseases clinic before

Exclusion criteria

Exclusion Criteria:

  • Not registered for a Psychiatric Nursing course.
  • Having previously taken a Psychiatric Nursing course.
  • Not attending class regularly.
  • Having previously received training with a schizophrenia simulation.
  • Having previously practiced in a Mental Health and Diseases clinic.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
32 participants (estimated)

Study arms

  • Experimental
    Virtual reality simulation of a patient with schizophrenia

    Virtual reality simulation will be applied to psychiatric nursing course students. The same students will participate in the theoretical and practical training of the psychiatric nursing course

    Other: Virtual Reality Simulation

  • No intervention
    Control: Standard psychiatric nursing education

    The control group will receive standard psychiatric nursing education consisting of theoretical lectures and routine clinical practice without VRS

Interventions

  • OtherVirtual Reality Simulation

    Virtual reality simulation of a patient with schizophrenia

06

What researchers measure

Primary outcomes

  1. Clinical decision-making skills assessed by the Clinical Decision-Making Scale

    Clinical decision-making skills of psychiatric nursing students will be measured using the Clinical Decision-Making Scale at baseline, mid-term, and end of academic term.

    Time frame: Baseline, mid-term (week 8), and end of academic term (week 16)

  2. Self-confidence assessed by the Self-Confidence Scale

    Self-confidence levels of psychiatric nursing students will be measured using the Self-Confidence Scale at baseline, mid-term, and end of academic term

    Time frame: Baseline, mid-term (week 8), and end of academic term (week 16)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Orchid ID: https://orcid.org/0000-0003-0077-9264

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2026 (actual). Primary completion is estimated for Jun 2026, 3 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 21, 2025
First posted
Jun 23, 2026
StartActual
Mar 1, 2026
Primary completionEst.
Jun 30, 2026
CompletionEst.
Jul 1, 2026
Last update
Jun 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07663851
Lead sponsor
Istanbul Arel University
Responsible party
Arzu DIKICI (Assistant Professor, Istanbul Arel University) — Principal investigator
First posted
Jun 23, 2026
Start date
Mar 1, 2026
Primary completion
Jun 30, 2026 (estimated)
Completion
Jul 1, 2026 (estimated)
Last update
Jun 23, 2026

Study contacts

Arzu DİKİCİ, Dr.
Contact
arzudikici@arel.edu.tr
0530 037 21 80

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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