Muğla Sıtkı Koçman University, Fethiye Health Services Vocational School
Muğla, 48300, Turkey (Türkiye)
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Ali AKGÜN, PhD(c)
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Süreyya GÜMÜŞSOY, Assoc. Prof.
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NCT Number: NCT07361835
This research is a randomized controlled study designed to develop and evaluate the effectiveness of a video-based virtual reality (VR) simulation for prehospital intervention training of crush syndrome for paramedic students. The study aims to examine the impact of VR simulation on knowledge levels, satisfaction, and sense of presence among second-year first and emergency aid students at Muğla Sıtkı Koçman University.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Muğla, 48300, Turkey (Türkiye)
Ali AKGÜN, PhD(c)
CONTACT
Süreyya GÜMÜŞSOY, Assoc. Prof.
CONTACT
The study will be conducted with second-year students enrolled in the first and emergency aid program at Muğla Sıtkı Koçman University, Fethiye Health Services Vocational School. Participants will be assigned to experimental and control groups using simple randomization. The experimental group will receive training via virtual reality (VR) simulation, while the control group will receive traditional theoretical education. Knowledge levels, technology use, satisfaction, and sense of presence will be measured using various validated scales.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Being a second-year student currently enrolled in the first and emergency aid program at Muğla Sıtkı Koçman University.
Voluntarily providing written informed consent to participate in the study. Having basic technological literacy to use virtual reality equipment.
Exclusion criteria
First-year students who have not yet reached the relevant stage of the curriculum.
Students who have previously participated in a similar virtual reality-based crush syndrome simulation.
Students with medical conditions that may be aggravated by VR use (e.g., severe motion sickness, history of seizures).
Refusal to participate voluntarily.
A scenario-based three-dimensional virtual reality training program focusing on prehospital crush syndrome assessment and management.
Conventional theoretical classroom instruction on prehospital crush syndrome assessment and management.
Time frame: Baseline (pre-test) and immediately after the training session (post-test).
The knowledge level of participants is measured using the full 'prehospital crush syndrome knowledge level scale'. The scale consists of 32 items covering four sub-dimensions: general knowledge (12 items), treatment (9 items), transport (6 items), and advanced knowledge (5 items). Each correct answer is scored as 1 point, while incorrect or 'no idea' answers are scored as 0. The total score ranges from a minimum of 0 to a maximum of 32. A higher total score indicates a better understanding and a higher knowledge level of prehospital crush syndrome management.
Time frame: Immediately after completion of the training intervention.
Participant satisfaction with the educational method (virtual reality or theoretical lecture) is measured using the 'education method satisfaction form'. This is a single-item numeric rating scale ranging from a minimum of 0 to a maximum of 10. A score of '0' indicates that the participant is not at all satisfied with the teaching method, while higher scores indicate increasing levels of satisfaction, with a score of '10' representing full satisfaction. Higher scores mean a better outcome.
Time frame: Immediately after completion of the virtual reality training session
The sense of presence in the virtual reality environment is measured using the 'presence questionnaire'. This scale assesses various dimensions such as involvement, sensory fidelity, and adaptation. Each item is scored on a 5-point likert scale, ranging from a minimum of 1 to a maximum of 5. For instance, a score of '1' indicates no presence or very poor quality, while a score of '5' indicates a high level of presence or complete naturalness. A higher total score indicates a greater sense of presence and a more immersive virtual reality experience.
Time frame: Baseline (pre-test)
Participants' orientation and interest towards technology are measured using the 'technology usage scale'. This scale consists of 13 items scored on a 5-point likert scale (1 = strongly disagree to 5 = strongly agree). The total score ranges from a minimum of 13 to a maximum of 65. A higher total score indicates a higher level of technology integration, interest, and adaptation to technological innovations in daily life.
Time frame: Immediately after completion of the training session
Participants' attitudes toward using virtual reality for learning and professional development are measured using the 'virtual reality attitude scale'. The scale consists of 9 items scored on a 5-point likert scale (1 = strongly disagree to 5 = strongly agree). The total score ranges from a minimum of 9 to a maximum of 45. A higher total score indicates a more positive attitude and higher perceived usefulness regarding the integration of virtual reality into educational processes
Contact information is provided by the study sponsor or research team.
Ali AKGÜN, PhD(c)
CONTACT
Süreyya GÜMÜŞSOY, Assoc. Prof.
CONTACT
Ege University
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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