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Disaster; PersonalityNCT06253156

The Effect of Virtual Reality-Based Disaster Education Given to Nursing Students on Disaster Preparedness

A study testing virtual reality in people with Disaster; Personality and Disorder, Mood, run by Baskent 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

It is thought that, as a result of the virtual reality-based disaster training given to nursing students, the psychological preparedness of nursing students who will work before, during and after the disaster will increase in disaster preparedness and disaster threat. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Disaster; Personality, Disorder, Mood
What is being tested?
virtual reality
Could I receive a placebo?
No, everyone receives an active treatment
How many people
67 participants
Where
1 siteTurkey (Türkiye)
Study dates
29 Feb 2024to 29 Apr 2024
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 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Being a 3rd and 4th year nursing student at the relevant universities where the study will be conducted,
  • Not having taken the disaster management course before,
  • Not having any health problems related to vision and hearing,
  • Not wearing glasses to be able to use virtual reality (VR) glasses

Who cannot join

  • Having any problems with vision or hearing
  • Using glasses

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Başkent University

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Virtual Reality-Based Disaster Education Given to Nursing Students on Disaster Preparedness: Randomized Controlled Study

It is thought that, as a result of the virtual reality-based disaster training given to nursing students, the psychological preparedness of nursing students who will work before, during and after the disaster will increase in disaster preparedness and disaster threat. It is thought that this research will lead to the development of school-based interventions at other universities in similar situations.

The purpose of this research is to increase the level of psychological preparation and awareness of disaster preparedness and disaster threat through virtual reality-based disaster education given to nursing students.

Being tested
virtual reality
Keywords
Disaster, Disaster Preparedness, Psychological Preparedness, Nursing Students, Virtual Reality
Medical subject headings
Mood Disorders

What participants receive

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

  • virtual realityBehavioural

    It is planned to provide 4 sessions of standard disaster preparedness training to nursing students in the intervention group. After the standard training sessions are completed, nursing students will be shown disaster simulation videos and visuals using virtual reality glasses within the scope of the virtual reality-based disaster preparedness training program.

Study groups in NCT06253156
Study groupRoleWhat they receive
virtual realityExperimentalThe experimental group will be given virtual reality-based training in addition to standard training.
Receives: Behavioral: virtual reality
standard trainingNo interventionThe control group will be given only standard training.

What is being measured

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

  1. DİSASTER PREPARATION

    Disaster preparedness level will be evaluated with the Disaster Threat Preparedness and Psychological Preparedness Scale. The minimum score that can be obtained from the scale is 13 and the maximum score is 52. As the score obtained from the scale increases, readiness also increases.

    Measured: 1-2 mounth

Timeline

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

  1. First posted12 Feb 2024
  2. Study start29 Feb 2024
  3. Primary completion19 Mar 2024
  4. Study completion29 Apr 2024

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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
67 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06253156
Sponsor's protocol ID
BASKENTUNIVERSITY-001
Status last verified
Aug 2024
First submitted
2 Feb 2024
Last updated
7 Aug 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Ertugrul B, Ugurlu Z. The effect of virtual reality based disaster training on disaster preparedness of nursing students: a randomized controlled study. BMC Nurs. 2026 Feb 4;25(1):207. doi: 10.1186/s12912-026-04373-w.

    PubMed 41634742

Questions about this trial

What is this clinical trial studying?

A study testing virtual reality in people with Disaster; Personality and Disorder, Mood, run by Baskent 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 4 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 7 Aug 2024. 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?

DİSASTER PREPARATION (time frame: 1-2 mounth). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06253156, which also lists 1 linked publication.

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 7 Aug 2024.

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