Mental Rotation, 3D Perception, and Practical Skill Development in Physiotherapy Students

November 20, 2025 updated by: Ramazan KURUL, Abant Izzet Baysal University

The Impact of Mental Rotation and 3D Perception Abilities on the Development of Practical Skills in Physiotherapy and Rehabilitation Students

This study investigates the role of mental rotation and 3D perception abilities in shaping the practical skill performance of physiotherapy and rehabilitation students. By exploring the relationship between spatial cognitive abilities and hands-on competencies, the research aims to provide insights that may improve educational strategies and clinical training outcomes.

Study Overview

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

Interventional

Enrollment (Actual)

118

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 Locations

      • Bolu, Turkey (Türkiye), 14300
        • Bolu Abant Izzet Baysal University Department of Physiotherapy and Rehabilitation

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

  • Adult

Accepts Healthy Volunteers

Yes

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

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: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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
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.
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
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Grade Point Average (GPA)
Time Frame: Baseline, eight weeks and 48 months
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.
Baseline, eight weeks and 48 months
Purdue Spatial Visualization Test: Rotations (PSVT-R)
Time Frame: Baseline, eight weeks and 48 months
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.
Baseline, eight weeks and 48 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Corsi Block-Tapping Test
Time Frame: Baseline and eight weeks
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
Baseline and eight weeks
Test Anxiety Inventory
Time Frame: Baseline and eight weeks
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.
Baseline and eight weeks
Enjoyment and Recommendation
Time Frame: Baseline and eight weeks
Participants will fill out a feedback questionnaire regarding the learning instruments using visual analogue scale (0-100mm).
Baseline and eight weeks
Test Taking Motivation Questionnaire
Time Frame: Baseline and eight weeks
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.
Baseline and eight weeks
Mental Rotation Test
Time Frame: Baseline and eight weeks
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.
Baseline and eight weeks
Puzzle Assembly
Time Frame: Baseline and eight weeks
Participants were asked to complete 3d printed puzzle of bone fractures and completion time was tracked.
Baseline and eight weeks
CarMen-Q
Time Frame: Baseline and eight weeks
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.
Baseline and eight weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: ramazan kurul, phd, Abant Izzet Baysal University

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 (Actual)

September 1, 2020

Primary Completion (Actual)

July 30, 2025

Study Completion (Actual)

September 30, 2025

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

November 17, 2025

First Posted (Estimated)

November 21, 2025

Study Record Updates

Last Update Posted (Actual)

November 25, 2025

Last Update Submitted That Met QC Criteria

November 20, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • AIBU-FTR-RK-13

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The dataset can be obtained from the principal investigator upon any reasonable request.

IPD Sharing Time Frame

After publication of the research.

IPD Sharing Access Criteria

ramazankurul@ibu.edu.tr

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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