Virtual Reality-Based Motor Imagery for Individuals With Low Imagery Ability: A Pilot Investigation of Isokinetic Strength and Electromyographic Activity
1 other identifier
interventional
32
1 country
1
Brief Summary
Motor imagery is a cognitive technique in which individuals mentally rehearse a movement without physically performing it. However, individuals with low imagery ability may not fully benefit from traditional motor imagery training. Virtual reality (VR) may enhance imagery vividness by providing immersive visual feedback. The purpose of this study is to compare the effects of immersive VR-based motor imagery, action observation combined with motor imagery, kinesthetic motor imagery alone, and a control condition on imagery ability, muscle strength, and muscle activation. Thirty-two healthy male participants will be assigned to one of four parallel groups based on imagery ability levels. All participants will complete a 4-week unilateral leg extension resistance training program (three sessions per week at 80% of one-repetition maximum). During each session, participants will perform their assigned imagery protocol. Primary outcomes include changes in imagery ability assessed by the Movement Imagery Questionnaire-3. Secondary outcomes include isokinetic quadriceps peak torque, average power, and surface electromyography activity of the rectus femoris, vastus medialis, and vastus lateralis muscles. The findings of this study may provide insight into whether immersive VR can enhance the effectiveness of motor imagery training in individuals with low imagery ability.
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 Aug 2025
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
Study Start
First participant enrolled
August 12, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 25, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 20, 2026
CompletedFirst Submitted
Initial submission to the registry
March 3, 2026
CompletedFirst Posted
Study publicly available on registry
March 10, 2026
CompletedMarch 10, 2026
March 1, 2026
5 months
March 3, 2026
March 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Imagery Ability (MIQ-3 Total Score)
Imagery ability will be assessed using the Movement Imagery Questionnaire-3 (MIQ-3). The total score change from baseline to post-intervention will be analyzed.
Baseline to 4 Weeks
Secondary Outcomes (2)
Isokinetic Quadriceps Strength (60°/s, 120°/s)
Baseline to 4 Weeks
Surface EMG Activity (%MVIC)
Baseline to 4 Weeks
Study Arms (4)
Action Observation + Motor Imagery (AOMI)
EXPERIMENTALParticipants perform action observation combined with kinesthetic motor imagery prior to each resistance training session for 4 weeks.
Kinesthetic Motor Imagery
EXPERIMENTALParticipants perform kinesthetic motor imagery alone prior to each resistance training session for 4 weeks.
Control
ACTIVE COMPARATORParticipants perform relaxation imagery prior to each resistance training session for 4 weeks.
Immersive Virtual Reality-Based Motor Imagery
EXPERIMENTALParticipants perform immersive first-person virtual reality-based motor imagery prior to each training session. The VR environment provides visual simulation of unilateral leg extension movements from a first-person perspective. The intervention is administered three times per week for 4 weeks before resistance training.
Interventions
VR Motor Imagery - Intervention Description Participants perform immersive first-person virtual reality-based motor imagery prior to each training session. The intervention is administered three times per week for 4 weeks before resistance training.
Participants observe a video demonstration of unilateral leg extension while simultaneously performing kinesthetic motor imagery of the movement prior to each resistance training session, three times per week for four weeks.
Participants perform kinesthetic motor imagery of unilateral leg extension without visual assistance prior to each resistance training session, three times per week for four weeks.
Participants perform relaxation-based imagery unrelated to strength training prior to each resistance training session, three times per week for four weeks.
Eligibility Criteria
You may qualify if:
- Healthy male individuals aged 18-30 years No participation in a structured lower-limb resistance training program within the previous 6 months No prior experience with structured motor imagery training Provided written informed consent
You may not qualify if:
- History of lower-limb musculoskeletal injury or surgery within the past 6 months Neurological disorders affecting motor control Visual or vestibular impairments preventing safe use of virtual reality equipment Current use of medications affecting neuromuscular performance Any medical condition contraindicating resistance training
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ege University
Izmir, Bornova, 35355, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
March 3, 2026
First Posted
March 10, 2026
Study Start
August 12, 2025
Primary Completion
December 25, 2025
Study Completion
January 20, 2026
Last Updated
March 10, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- Data will be available beginning 6 months following publication of the primary results and will remain available for 5 years.
- Access Criteria
- Access to de-identified individual participant data will be granted to qualified researchers upon reasonable request to the corresponding author. Requests must include a brief research proposal outlining the intended use of the data. Data will be shared following approval by the study investigators and in accordance with institutional and ethical guidelines.
De-identified individual participant data (IPD) underlying the primary and secondary outcome measures, including MIQ-3 scores, isokinetic peak torque values, average power, and normalized sEMG data, will be shared. Demographic variables necessary for replication (age and body mass) will also be included.