Development of Hand Hygiene Training Virtual Reality Simulation and Evaluation of Its Effectiveness

January 23, 2025 updated by: Askin Selvi, Istanbul University - Cerrahpasa

Development of Hand Hygiene Training Virtual Reality Simulation and Evaluation of Its Effectiveness: an Example of In-Service Training in Nursing

Healthcare-associated infections (HAI), which have become a major problem in all countries, prolong hospital stay and increase treatment and care costs. In health care institutions, HAIs that occur directly or indirectly related to health services are among the most common causes of mortality and morbidity. A high level of hand hygiene compliance, which is the most basic step of infection control and precautions, is the first and most important step to prevent HAIs. However, it has been determined in the literature that the compliance rates of healthcare professionals with hand hygiene are low and that nurses' attitudes and behaviors regarding hand hygiene are not at the desired level. Well-structured training programs need to be developed to maintain and increase nurses' hand hygiene compliance rates. Different training methods and tools are needed to increase hand hygiene compliance, awareness and awareness. It is recommended that innovative training approaches such as virtual simulation be developed and evaluated to further internalize and encourage nurses' most effective hand hygiene practice behaviors. In recent years, the use of simulation methods in the training of healthcare professionals has been increasing as they facilitate the transfer of theoretical knowledge into clinical practice. One of these simulation methods is virtual reality (VR). The use of gamification in the virtual environment supports different learning styles, enabling learners to participate more intensively in education and increase their internal motivation. In this context, with VR support, entertainment and learning processes can be used to support each other. Considering the features of VR usage such as integrating knowledge and skills, creating a learning environment for the learner by doing, giving the opportunity to repeat until the correct application is made, reducing incorrect interventions in clinical practice and increasing patient safety, it is recommended that virtual simulation systems be used in nursing education. VR provides different opportunities to learners by enriching and diversifying learning environments. In these virtual environments, learners can have new experiences and these experiences remain permanent for the learners. As stated in the WHO Hand Hygiene Theme, it is important to develop innovative training programs, learning materials and measurement and evaluation tools regarding hand hygiene within the scope of infection control and prevention studies. VR simulation can be used to attract nurses' attention and awareness by increasing intrinsic motivation to perform hand hygiene, and can be used to support nurses in developing positive attitudes towards hand hygiene. Hand hygiene simulation scenarios created with virtual reality can contribute to greater awareness about the problems caused by microorganism transmission by increasing hand hygiene awareness. Thus, increasing attitudes and awareness regarding hand hygiene can have a positive effect on reducing the HAI rate by supporting the transformation of hand hygiene awareness into behavior. In the study, it was planned to develop, implement and evaluate a virtual reality hand hygiene simulation. It is thought that this virtual reality simulation will pave the way for the development of psychomotor skills for hand hygiene, increase the level of knowledge, and increase hand hygiene compliance by providing internal motivation to perform hand hygiene. In our country, no studies have been found on the development of virtual reality simulation in hand hygiene practice. The aim of this study is to develop and implement virtual reality hand hygiene simulation in teaching hand hygiene behaviors in nurses and to evaluate its effect on hand hygiene compliance.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

76

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Nurses who have not received additional hand hygiene training after general orientation training at the beginning of work • Nurses working actively in areas other than the operating room (inpatient services, intervention units, etc.).

Exclusion Criteria:

  • Nurses in the intervention group who have a disease/condition that may pose a problem regarding the use of VR glasses (having epilepsy, having a history of seizures, having an eye or neurological disease that would prevent the use of VR glasses, having motion sickness).

    • Nurses working in the operating room
    • Nurses who receive additional hand hygiene training after general orientation training

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: experimental group
After giving 360 hours of hand hygiene theoretical training to the participants in the experimental group, a hand hygiene virtual reality simulation application will be performed.
Other: control group
Participants in the control group will receive only 360 hours of hand hygiene theoretical training. Participants in this group will not be given hand hygiene virtual reality simulation application.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Introductory Form
Time Frame: up to one month
It is an introductory form prepared by the researcher as a result of a literature review, which includes questions about the socio-demographic characteristics of the participants, their current situation in the working environment regarding hand hygiene, and their opinions about hand hygiene.
up to one month
Knowledge Test
Time Frame: up to 12 weeks
It is a form prepared by the researcher after a literature review to evaluate the level of knowledge about hand hygiene to be applied before and after hand hygiene training and will be used after validity and reliability analysis.
up to 12 weeks
Scale for Evaluation of Hand Washing Behavior in Terms of Planned Behavior Model
Time Frame: up to 12 weeks
The scale was developed to collect information about the knowledge, attitudes and behaviors of healthcare personnel regarding hand washing and to identify deficiencies. The scale consists of 8 sub-dimensions and a total of 46 items related to knowledge, attitudes and behaviors towards hand washing. The lowest score that can be obtained from the scale is 46, the highest score is 176. A high score indicates a positive and strong motivation to wash hands.
up to 12 weeks
Hand Hygiene Observation Form
Time Frame: up to 12 weeks

This form is prepared with reference to the World Health Organization and is marked by observing hand hygiene behaviors in clinics. In the Hand Hygiene Observation Form, the observed indications are classified as the appropriate time for hand hygiene (denominator) used to measure the actual hand hygiene action (action serving as the numerator). These two variables determine the compliance to be calculated. Compliance results can be calculated overall, but can also be divided into occupational categories and indications. Compliance with hand hygiene is the ratio of the number of actions to the number of appropriate times and is expressed by the following formula:

Compliance (%) = Number of WASHES and/or SCRUBS × 100 / Number of Indications

Compliance by Indication (%) = Number of WASHES and/or SCRUBS × 100 / Number of Indications

up to 12 weeks
Simulation Design Scale
Time Frame: up to 12 weeks
The scale is evaluated in 2 parts. In the first part; It is evaluated whether the best simulation design elements can be applied in the simulation application. In the second part; It evaluates how important the simulation design elements are for the participants. The first section is evaluated as "strongly disagree with the statement", "disagree with the statement", "undecided", "agree with the statement", "strongly agree with the statement" and "not appropriate". The second section is evaluated as "not important", "partially important", "undecided", "important", "very important". Scale scores are obtained by dividing the sum of the total and sub-dimension scores by the number of items.
up to 12 weeks
Training Evaluation Form
Time Frame: up to 12 weeks
It is a form prepared for participants to evaluate the purpose of the training program, training activities, satisfaction level with the program, training environment and educator. It is not a scale, but a form prepared by the researcher.
up to 12 weeks
Student Satisfaction and Self-Confidence Scale in Learning
Time Frame: up to 12 weeks
It is a scale that determines the satisfaction level of the participants towards the simulation application. Scale scores are obtained by dividing the total of the sub-dimensions by the number of items. As the total score from the scale increases, student satisfaction and self-confidence in learning also increase.
up to 12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: AŞKIN SELVİ, PhD student, İstanbul University-Cerrahpasa, Turkey

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 25, 2025

Primary Completion (Estimated)

March 25, 2025

Study Completion (Estimated)

May 25, 2025

Study Registration Dates

First Submitted

April 12, 2024

First Submitted That Met QC Criteria

January 22, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 23, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • İUC_ASELVİ_001
  • Hülya Kaya (Other Identifier: Bezm-i Alem Foundation University)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Study Protocol Statistical Analysis Plan Informed Consent Form Clinical Study Report Analytic Code

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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