- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03376334
A Pilot Study to Investigate the Effect of Motor Imagery on Dynamic Balance of Asymptomatic Students
December 12, 2017 updated by: Pramod Divakara Shenoy, MPT, Universiti Tunku Abdul Rahman
A Pilot Study to Investigate the Effect of Motor Imagery on Dynamic Balance of Asymptomatic University Students: An Experimental Study
This study intended to investigate the effect of imagining a movement task on dynamic balance of sedentary university students.
Two groups with good mental imaging ability were studied; one group receiving instructions on mental imagery and the other served as a control receiving no particular intervention.
Any improvement in the balance ability was measured using the star excursion balance test (SEBT); for it has good to excellent test-retest reliability and validity as established by several researchers.
Study Overview
Detailed Description
Motor imagery (MI) refers to a cognitive process during which the representation of a specific motor action is internally simulated without producing an overt body movement.
Motor imagery is now widely used as a technique to enhance motor learning and to enhance recovery during rehabilitation of various conditions such as sports injuries, stroke, etc.
Several studies have also shown improvement in strength, function, and use of both upper and lower extremities in chronic stroke.
Present study aimed to identify its effectiveness in improving dynamic balance of individuals without any clinical problem.
Such improvement, if any, may be useful in early balance and proprioceptive training during the maximum protection phase of joint injuries, fractures, or even rehabilitation of other clinical conditions affecting balance.
It may have benefits in maintaining / improving movements in athletes after injuries as well as the general less active population, including the elderly population.
Study Type
Interventional
Enrollment (Actual)
25
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
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Selangor
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Cheras, Selangor, Malaysia, 43000
- Universiti Tunku Abdul Rahman
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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
18 years to 25 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- No prior involvement in any physical or mental balance training
- Good mental imaging ability as determined using the motor imagery questionnaire
Exclusion Criteria:
- neuromusculoskeletal condition that may alter balance
- vestibular disorders or VBA related disorders
- painful conditions of the body
- H/o seizure, schizophrenia, meningitis, migraine, diplopia, spinal injuries, lower extremity injuries
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: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Motor Imagery (MI)
Those meeting the inclusion criteria were selected (n=22).
Each participant was necessary to complete the Movement Imagery Questionnaire in a quiet room.
Finally, each participant assigned a score by using a 7-point scale regarding the ease/difficulty associated with representing each movement mentally.
Next their baseline balance measurement was performed using the SEBT.
Later this group had 9 motor imagery sessions, each session for 15 minutes, 3 sessions (alternate days) per week for a total of 3 weeks.
Reassessment of balance was done after every 3 sessions.
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NO_INTERVENTION: Control (C)
Those meeting the inclusion criteria were selected (n=10).
Baseline measurement of SEBT was done on day 1, end of week 1, end of week 2 and end of week 3.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dynamic Balance
Time Frame: 24 days
|
Ability to balance while performing a task i.e. lower limb reach distance is various directions measured using star excursion balance test
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24 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time for improvement in balance
Time Frame: 7 to 24 days
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Time required to observe a significant improvement in balance
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7 to 24 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Yee Mun Chang, Alumnus of Universiti Tunku Abdul Rahman
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
October 2, 2014
Primary Completion (ACTUAL)
May 25, 2015
Study Completion (ACTUAL)
May 25, 2015
Study Registration Dates
First Submitted
December 12, 2017
First Submitted That Met QC Criteria
December 12, 2017
First Posted (ACTUAL)
December 18, 2017
Study Record Updates
Last Update Posted (ACTUAL)
December 18, 2017
Last Update Submitted That Met QC Criteria
December 12, 2017
Last Verified
December 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- U/SERC/40/2014
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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