Virtual Reality Infection Control Training for Healthcare Workers During the Hajj Season
(VIRTIC-Hajj)
Virtual Reality Training for Infection Control Preparedness in Healthcare Practitioners During Hajj: A Randomized Controlled Trial on Skill Acquisition and Clinical Readiness
1 other identifier
interventional
200
0 countries
N/A
Brief Summary
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?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 1, 2025
CompletedFirst Posted
Study publicly available on registry
August 8, 2025
CompletedStudy Start
First participant enrolled
January 20, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 21, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
August 8, 2025
August 1, 2025
1 year
August 1, 2025
August 1, 2025
Conditions
Keywords
Outcome Measures
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.
From enrollment to 1 week post-training
Secondary Outcomes (1)
Change in Self-Reported Preparedness and Confidence in Infection Control
From enrollment to 1 week post-training
Study Arms (2)
VR infection control training
EXPERIMENTALDelivered via a headset-based immersive environment designed specifically for Hajj mass gathering scenarios. Training duration is 30-40 minutes and includes interactive modules and performance-based feedback.
Traditional Training Arm
NO INTERVENTIONParticipants in this arm will attend a standard infection control lecture, presented in PowerPoint format by an infection control expert. Content mirrors the topics covered in the VR module but is delivered passively.
Interventions
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.
Eligibility Criteria
You may qualify if:
- Aged 20 and above
- Assigned to work in Hajj healthcare settings
- Licensed healthcare worker (nurse, physician, EMT, etc.)
- Able to provide informed consent
- Fluent in Arabic or English
You may not qualify if:
- History of epilepsy or motion sickness triggered by VR
- Severe visual or cognitive impairments
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Links
Study Officials
- STUDY DIRECTOR
Noha M Ibrahim, PhD
University of Bisha
- PRINCIPAL INVESTIGATOR
Mohammed O Alanazi, PhD
University of Bisha
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. Mohammed Alanazi, PhD, MSN, RN
Study Record Dates
First Submitted
August 1, 2025
First Posted
August 8, 2025
Study Start
January 20, 2026
Primary Completion (Estimated)
January 21, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
August 8, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share
This study will not share individual participant data due to institutional privacy policies and ethical constraints related to healthcare worker data during mass gathering events.