Virtual Reality Infection Control Training for Healthcare Workers During the Hajj Season

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20+
SponsorUniversity of Bisha

About this trial

The goal of this clinical trial is to evaluate the effectiveness of immersive virtual reality (VR) training on improving infection control preparedness among healthcare workers during the Hajj pilgrimage in Saudi Arabia.

The main questions this study aims to answer are:

Does VR training improve healthcare workers' knowledge, confidence, and preparedness for infection control compared to traditional training?

Are there differences in outcomes between the VR training and traditional lecture-based education?

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Aged 20 and above

Assigned to work in Hajj healthcare settings

Licensed healthcare worker (nurse, physician, EMT, etc.)

Able to provide informed consent

Disqualifiers

History of epilepsy or motion sickness triggered by VR

Severe visual or cognitive impairments

Trial design

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality Infection Control Training

    Device

    This study evaluates a VR training program designed specifically to improve infection control skills among healthcare workers during the Hajj pilgrimage, one of the world's largest mass gatherings. Unlike traditional training, this VR intervention offers immersive, realistic simulations tailored to the unique cultural and environmental challenges of Hajj. It focuses on practical skill-building and clinical readiness in crowded, high-risk settings. Using a rigorous randomized controlled trial design, the study aims to show that VR training is more effective than conventional methods, potentially setting a new standard for infection control education in mass gathering healthcare.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: VR infection control trainingExperimental treatment 1 intervention
Group B: Traditional Training ArmNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Change in Infection Control Knowledge Score From Baseline to Post-Training

Participants will complete a validated multiple-choice infection control knowledge test. Scores range from 0 to 100, with higher scores indicating greater knowledge. A score improvement of ≥15% is considered clinically meaningful.

Time frame
From enrollment to 1 week post-training

Secondary outcomes

1

Change in Self-Reported Preparedness and Confidence in Infection Control

Measured using a 5-point Likert scale (1 = not confident; 5 = very confident). Participants with an increase of ≥1 point in average scores from baseline are considered to have improved.

Time frame
From enrollment to 1 week post-training

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: