NCT07886866

Brief Summary

This study evaluated the effect of three-dimensional (simulations) virtual reality-based disaster training with simulation on disaster readiness among health science students. The study used a randomized controlled design. Participants assigned to the intervention group received disaster training using 3D virtual reality technology and simulation, while participants in the control group received usual education or training. Outcomes were assessed at baseline before the intervention, after completion of the training, and at a subsequent follow-up assessment. The study aimed to evaluate the effects of simulations virtual reality-based simulation training on disaster readiness over time.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
110

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2026

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 15, 2026

Completed
29 days until next milestone

First Submitted

Initial submission to the registry

October 14, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 21, 2026

Completed
Last Updated

October 21, 2026

Status Verified

October 1, 2026

Enrollment Period

5 months

First QC Date

October 14, 2026

Last Update Submit

October 14, 2026

Conditions

Keywords

Virtual RealityThree-Dimensional SimulationDisaster PreparednessDisaster ReadinessHealth Science StudentsDisaster Education

Outcome Measures

Primary Outcomes (1)

  • Change in Disaster Readiness Score From Baseline to Post-Training

    Change in disaster readiness among health science students from baseline before the intervention to immediately after completion of training, assessed using the published measurement instrument used in the study.

    Baseline before the intervention to immediately after completion of training.

Secondary Outcomes (1)

  • Disaster Readiness Score at 8-Week Follow-Up

    8 weeks after completion of the training.

Study Arms (2)

Virtual Reality-Based Disaster Training

EXPERIMENTAL

Participants received disaster training using simulations virtual reality technology and simulation

Behavioral: simulations Virtual Reality-Based Disaster Training With Simulation

Usual Education or Training

NO INTERVENTION

Participants received disaster training without using simulations virtual reality technology and simulation

Interventions

Participants in the intervention group received disaster training using three-dimensional virtual reality technology and simulation. The training was designed to provide an immersive learning experience involving disaster scenarios to support disaster readiness among health science students. The intervention was delivered according to the study protocol.

Virtual Reality-Based Disaster Training

Eligibility Criteria

Age18 Years - 28 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Students enrolled in the participating health sciences programs at the study institution.
  • Students who met the study's age and participation requirements.
  • Students who provided informed consent to participate.

You may not qualify if:

  • Students who declined to participate or did not provide informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vision Colleges

Riyāḑ, 3422, Saudi Arabia

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 14, 2026

First Posted

October 21, 2026

Study Start

April 1, 2026

Primary Completion

September 1, 2026

Study Completion

September 15, 2026

Last Updated

October 21, 2026

Record last verified: 2026-10

Locations