- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07241026
Mental Rotation, 3D Perception, and Practical Skill Development in Physiotherapy Students
The Impact of Mental Rotation and 3D Perception Abilities on the Development of Practical Skills in Physiotherapy and Rehabilitation Students
Study Overview
Status
Conditions
Detailed Description
Practical skills are fundamental to physiotherapy and rehabilitation education, requiring students to accurately interpret anatomical structures, movement patterns, and therapeutic techniques in three-dimensional space. Cognitive abilities such as mental rotation and 3D perception are considered essential in processing spatial information and transferring theoretical knowledge into clinical practice. However, limited research has explored how these spatial abilities influence the acquisition and execution of practical competencies in physiotherapy training.
This study aims to assess the relationship between mental rotation ability, 3D spatial perception, and the practical performance of physiotherapy and rehabilitation students. Standardized spatial ability tests will be used alongside practical skill assessments to identify correlations between cognitive factors and clinical task execution. The findings are expected to contribute to curriculum design by highlighting the importance of integrating spatial training modules and potentially guiding student selection or tailored support strategies.
The aim of this study is to examine the impact of mental rotation and 3D perception abilities on the development and performance of practical skills in physiotherapy and rehabilitation students, with the goal of enhancing educational methods and optimizing clinical training outcomes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Bolu, Turkey (Türkiye), 14300
- Bolu Abant Izzet Baysal University Department of Physiotherapy and Rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Willingness to participate and provide written informed consent
- Normal or corrected-to-normal vision
Exclusion Criteria:
- History of neurological or musculoskeletal disorders affecting upper-limb function or spatial cognition
- Severe visual impairments that cannot be corrected
- History of epilepsy, severe motion sickness, or vestibular disorders
- Participation in other spatial-cognition or VR-based training programs within the last 6 months
- Use of medications affecting cognitive function or balance
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: 3D spatial cognition training and mental rotation
Participants will receive a structured mental rotation and 3D spatial cognition training program, consisting of immersive virtual reality (VR) practice, computerized rotation tasks, and hands-on spatial exercises
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Participants will undergo a 60-minute training session, consisting of immersive 3D/VR practice, computerized mental rotation tasks, and hands-on spatial exercises.
Each session will begin with a 20-minute VR-based activity in which students interact with anatomical models and 3D objects, rotating and orienting them to match different views and cross-sections.
This will be followed by a 20-minute computerized module, where participants complete adaptive mental rotation tasks of varying angular disparity, including both object-based and body-posture items.
The final 15-20 minutes will include practical spatial exercises, such as assembling 3D anatomical puzzles, reach-and-place tasks, and proprioceptive orientation drills.Training will be delivered 3 days per week for 8 weeks.
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Sham Comparator: Sham 3D spatial cognition training and mental rotation
Participants will receive a sham mental rotation and 3D spatial cognition program, consisting of non-spatial computerized tasks and general educational activities without targeted spatial training
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Participants will undergo a 60-minute training session, consisting of non-spatial computerized tasks, general cognitive exercises, and low-demand hands-on activities.
Each session will begin with a 20-minute computer-based activity presenting neutral content, such as quizzes, word puzzles, or simple problem-solving tasks, without requiring 3D manipulation or mental rotation.
This will be followed by a 20-minute module of general cognitive tasks, including memory or attention exercises unrelated to spatial orientation.
The final 15-20 minutes will include low-intensity hands-on activities, such as organizing materials or following simple step-by-step instructions, designed to match the duration and engagement of the intervention arm without targeting spatial cognition.
Training will be delivered 3 days per week for 8 weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Grade Point Average (GPA)
Time Frame: Baseline, eight weeks and 48 months
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To evaluate the overall academic performance of participants, Grade Point Average (GPA) will be collected from university records.
GPA is calculated on a 4.0 scale, with 0.0 representing failing performance and 4.0 representing excellent academic achievement.
Higher scores indicate better academic performance.
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Baseline, eight weeks and 48 months
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Purdue Spatial Visualization Test: Rotations (PSVT-R)
Time Frame: Baseline, eight weeks and 48 months
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To assess participants' spatial visualization and mental rotation abilities, the PSVT-R will be administered.
The test comprises 30 multiple-choice items, each with a single correct answer, scored 1 for correct and 0 for incorrect responses.
Total scores range from 0 to 30, with higher scores reflecting stronger spatial visualization skills.
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Baseline, eight weeks and 48 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Corsi Block-Tapping Test
Time Frame: Baseline and eight weeks
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Involves mimicking a sequence of up to nine spatially separated blocks tapped by the examiner.
The length of the longest sequence correctly recalled is the score.
Higher scores indicates better spatial abilities
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Baseline and eight weeks
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Test Anxiety Inventory
Time Frame: Baseline and eight weeks
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To examine whether there is a change in the level of anxiety experienced by students during the exam, a 5-question short version of Test Anxiety Inventory will be used.
The test includes sections related to ease, comfort associated with learning, and alignment of exam questions with the course.
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Baseline and eight weeks
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Enjoyment and Recommendation
Time Frame: Baseline and eight weeks
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Participants will fill out a feedback questionnaire regarding the learning instruments using visual analogue scale (0-100mm).
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Baseline and eight weeks
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Test Taking Motivation Questionnaire
Time Frame: Baseline and eight weeks
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To assess the level of motivation students exhibit during examinations, the Test Taking Motivation Questionnaire (TTMQ) will be administered.
The questionnaire includes items evaluating students' effort, engagement, persistence, and goal orientation during test situations.
Each item is rated on a Likert scale, and total scores generally range from 0 to 100, with higher scores indicating greater motivation and engagement in test-taking activities.
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Baseline and eight weeks
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Mental Rotation Test
Time Frame: Baseline and eight weeks
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To evaluate the ability to mentally rotate three-dimensional objects, the Mental Rotation Test will be used.
The test includes 24 items, each with two correct answers.
Each correct response is awarded 1 point, resulting in a total score ranging from 0 to 24.
Higher scores indicate greater proficiency in mental rotation tasks.
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Baseline and eight weeks
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Puzzle Assembly
Time Frame: Baseline and eight weeks
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Participants were asked to complete 3d printed puzzle of bone fractures and completion time was tracked.
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Baseline and eight weeks
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CarMen-Q
Time Frame: Baseline and eight weeks
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Participants were asked to complete the CARMEN-Q (Cognitive Load, Motivation, and Emotion Questionnaire) to evaluate their perceived cognitive load and related psychological responses.
The scale includes four subscales: Intrinsic Load, Extraneous Load, Germane Load, and Affective-Motivational Factors (Motivation, Emotion, and Self-Efficacy).
Each item is rated on a 7-point Likert scale ranging from 1 (strongly disagree) to 7 (strongly agree).
Higher scores on the cognitive load subscales reflect greater perceived mental effort, while higher scores on motivation, emotion, and self-efficacy indicate more positive learner engagement and affective response.
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Baseline and eight weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: ramazan kurul, phd, Abant Izzet Baysal University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AIBU-FTR-RK-13
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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