Developing and Examining the Effectiveness of an Eye Tracker for Simulation Training
1 other identifier
interventional
40
1 country
1
Brief Summary
Today, rapid developments in technology and science; affected the economic, cultural, political and social fields. The use of technology in these areas has become a necessity rather than a privilege. Education is one of the areas where technology is used the most and most intensely affected. Different education and training technologies can be used at every stage of the education and training process. With the effective and correct use of technology, it is possible to provide efficient and effective service in the fields of education and health care. This situation is gaining more and more importance for our country in the fields of nursing practice and education. Nursing organizations accept technology as the basic building block of nursing education and practice. Simulation is defined as "a technique of developing real patient experiences and the most important aspects of the real world from experience using practice guides in a completely interactive way". According to the World Health Organization, the use of simulation methods for teaching and learning is one of the gold standards in nursing education. In the world, eye tracking systems are used to determine the focal point. Eye tracking technology aims to record the movement of the eyeball to determine where the person is focusing while performing certain tasks. These systems have also contributed to the study of cognitive and neurological development. It has started to be used together with simulation training in health education. By determining where the student focuses during clinical practice simulation training using an eye tracker, it is possible to reschedule the practice training or to provide feedback on the student's misapplications during the application. The purpose of this research; The aim of this study is to develop an eye tracker for simulation training in nursing and to examine the effectiveness of an eye tracker in a simulation scenario.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2022
Shorter than P25 for not_applicable
1 active site
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
February 17, 2022
CompletedStudy Start
First participant enrolled
March 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 15, 2022
CompletedFirst Posted
Study publicly available on registry
March 17, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
April 20, 2022
CompletedAugust 4, 2022
August 1, 2022
Same day
February 17, 2022
August 3, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Students' Satisfaction and Self-confidence Scale
This instrument is a 13-item scale used to measure student satisfaction with the simulation activity (5 items) and self-confidence in learning (8 items). Cronbach's alpha for satisfaction was 0.94; for self-confidence, it was 0.87. Responses are rated on a 5-point Likert scale with values ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores indicate higher satisfaction and greater levels of selfconfidence.
up to 2 weeks
Simulation Design Scale
The SDS is a 20-item tool developed to measure constructs from the Jeffries and Rizzolo (2006) simulation model. The design features rated by the students include objectives and information (five items), student support (four items), problem-solving (five items), guided reflection or feedback (four items), and fidelity (two items). Cronbach's alpha for the instrument was 0.92. Responses are rated on a 5-point Likert scale with values ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores indicate increased recognition of design features in simulation.
up to 2 weeks
Personal Information Form
The personal information form consists of a total of 9 questions about students' demographic information, reasons for choosing the nursing profession, and simulation experiences.
up to 2 weeks
Secondary Outcomes (1)
Wound dressing checklist
up to 2 weeks
Study Arms (2)
Experimental
EXPERIMENTALNo intervention
NO INTERVENTIONInterventions
Purpose: To develop a cost-effective and effective eye tracker for simulation training in nursing in Turkey. The wearable eye tracker consists of a front camera that will detect the pupil and determine the gaze region of the eye, and glasses or an alternative headband to which these cameras will be connected. A portable mini-computer will be used to process the obtained images. While recording and monitoring the eye movement with the pupil detection camera, real-world images in the user's field of view will be recorded by the front camera and the focal points will be determined. By establishing a linear connection between these found points, temperature (heat) maps will be created at the points where the eye looks.
Eligibility Criteria
You may qualify if:
- To be a 3rd year student at Pamukkale University nursing department in order to be included in the pilot study.
- To be a 4th year student of Pamukkale University nursing department in order to be included in the main application.
- Not working as a nurse in any institution (high school/associate graduate nurse).
- Volunteer to participate in the study.
You may not qualify if:
- Not being a student of Pamukkale University nursing department (3rd year student for pilot study-4th year student for main application) on the specified dates.
- Working as a nurse in any institution (high school / associate degree nurse).
- Not volunteering to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Aydin Adnan Menderes Üniversitesi
Aydin, 09100, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
February 17, 2022
First Posted
March 17, 2022
Study Start
March 15, 2022
Primary Completion
March 15, 2022
Study Completion
April 20, 2022
Last Updated
August 4, 2022
Record last verified: 2022-08