The Effect of Motor Imagery Dosage on Motor Learning in Healthy Adults
1 other identifier
interventional
27
2 countries
2
Brief Summary
The goal of this clinical trial is to compare the effects of different durations of Motor Imagery (MI) practice and physical practice on motor performance enhancement in healthy adults. The main questions it aims to answer are:
- Does Motor Imagery (MI) practice improve motor performance?
- How do different doses of MI practice (low vs. high) compare to no MI practice in enhancing motor performance? Participants:
- Be randomly assigned to one of three groups: no MI practice (control group), low dose MI practice (6 minutes per session), or high dose MI practice (12 minutes per session).
- Complete nine sessions over three weeks, practicing a timed mirror tracing task.
- Have their performance measured in each session by the time taken to complete the task and the number of errors made. Compared the control group, low dose MI group, and high dose MI group to see if there are significant differences in motor performance enhancement, aiming to determine the effectiveness of MI and the optimal dose for practice.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable healthy
Started Mar 2022
Shorter than P25 for not_applicable healthy
2 active sites
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
March 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 20, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
April 28, 2022
CompletedFirst Submitted
Initial submission to the registry
February 18, 2024
CompletedFirst Posted
Study publicly available on registry
March 7, 2024
CompletedMarch 12, 2024
March 1, 2024
2 months
February 18, 2024
March 7, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Time
The time to complete the physical tracing task was measured from when the investigator said 'GO' until the participant returned the pen to the starting point. The physical tracing task is a mirror tracing game that requires participants to trace a star shape viewed through a mirror, going as fast as possible while staying within the lines.
Time was measured at the end of each session, with intervals of 3 session/week for 3 weeks with total of 9 sessions. So, the research ended up with 9 reading for the time.
Errors
Errors were operationally defined as each time the pen went outside of the shape lines while doing the physical tracing task. Crossing a line and returning to the original trace was counted as one error. Errors were counted by the number of times the pen went outside the lines.
Errors were counted at the end of each session, with intervals of 3 session/week for 3 weeks with total of 9 sessions. So, the research ended up with 9 reading for the time.
Study Arms (3)
control group (CG)
SHAM COMPARATORPhysically performed the task once per session. No MI. The physical task is a mirror tracing game that requires participants to trace a star shape viewed through a mirror, going as fast as possible while staying within the lines.
low-dose group (LD)
EXPERIMENTALIn addition to physically performing the motor task once in session 1, then they performed MI for 6 minutes (2 min x 3 sets) per session. MI for this study took the form of non-guided first-person mental practice. First-person imagery was explained to each participant where they imagined performing the target skill through their own eyes rather than if they were a bystander watching someone else do the task (third person).
high-dose group (HD)
EXPERIMENTALIn addition to physically performing the motor task once in session 1, then MI for 12 minutes (2 min x 6 sets) per session. The MI technique was the same as the LD group.
Interventions
MI for this study took the form of non-guided first-person mental practice. First-person imagery was explained to each participant where they imagined performing the target skill through their own eyes rather than if they were a bystander watching someone else do the task (third person).
The participants performed the physical task only. It is a mirror tracing game that requires participants to trace a star shape viewed through a mirror, going as fast as possible while staying within the lines.
Eligibility Criteria
You may qualify if:
- no history of motor dysfunction, coordination disorders, or surgical procedures in the past 6 months
- scored 4 or less on the Movement Imagery Questionnaire (MIQ) on the non-dominant hand.
You may not qualify if:
- Played the target task in the past 6 months
- Subjects were ambidextrous
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Ahmed Mahmoud Kadrylead
- Concordia University Wisconsincollaborator
Study Sites (2)
Concordia University Wisconsin
Mequon, Wisconsin, 53097, United States
Kafrelshaikh University
Kafr ash Shaykh, 12623, Egypt
Study Officials
- PRINCIPAL INVESTIGATOR
Ahmed M Kadry, PhD
Associate Professor of Physical Therapy, Kafrelsheikh University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- The participants were blinded about which group they were allocated (control or intervention)
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Associate Professor of Physical Therapy
Study Record Dates
First Submitted
February 18, 2024
First Posted
March 7, 2024
Study Start
March 1, 2022
Primary Completion
April 20, 2022
Study Completion
April 28, 2022
Last Updated
March 12, 2024
Record last verified: 2024-03
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- 1 year from publication
- Access Criteria
- upon request from the principal investigator with appropriate justification
Data from this study, including individual participant data (IPD) and associated documentation, will be made available upon reasonable request to the principal investigator. Requests will be considered when accompanied by a detailed proposal, including a clear justification for the use of the data. Such requests will be subject to a review process to ensure compatibility with participant consent and the ethical guidelines governing the study. Data sharing will be facilitated under a data use agreement that specifies the terms and conditions to ensure the privacy and confidentiality of participants