- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05338918
Effect of Mental Imagery on Lower Limb Functions in Stroke
February 20, 2023 updated by: Riphah International University
Effects of Mental Imagery With Virtual Reality Training on Lower Limb Functions in Stroke
This study aims to compare the effects of mental imagery and virtual reality training with virtual reality alone on lower limb functional status of stroke patients.
The study will be a randomized controlled trial.
After the initial evaluation randomization will be done on participants lying under the eligibility criteria.
Randomized participants will be allocated to Control & Experimental groups.
Mental imagery (Audiotape recordings of some specific tasks for lower limb functions) with Virtual reality training given to experimental group while Virtual reality training alone to Control group.
Task oriented training for balance & gait as baseline treatment will be given to each group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Stroke causes inability to perform activities with affected limbs among which difficulty in walking and doing house chores are the most common dysfunctions.
Stroke highly affects the productivity of people in family as well as in community.
It also adds financial burden on families of patients.
There are number of different restorative techniques and therapeutic approaches for the rehabilitation of stroke patients.
For example, bobath approach, constrained induced movement therapy, mirror therapy, electrical stimulations, Circuit training, resistance training, Motor relearning program, proprioceptive neuromuscular facilitation, body weight supported treadmill for walking, Frenkel's exercises, repetitive task specific training, electromyography biofeedback and many others.
All these approaches mainly focused on the repetition of tasks to perform a specific function, as the neuroplasticity requires repetition to occur.
But there is a lack of interest, motivation and attention of stroke patients to perform similar tasks repeatedly.
The lack of active participation directly or indirectly affects the neural stimulation and neural plasticity.
One of the most emerging techniques in these days is Mental Imagery.
Mental imagery(MI) is "a training method where imagination of movements, without actually moving, is used with the intention of improving motor performance" Currently Mental imagery has been used for neuro rehabilitation as it activates the same brain areas required for planning and execution of movements more or less in the same way require for actual performance of that movement.
In this study the combination for Mental imagery and virtual reality is used for participation of patients in rehabilitation program which in turn increases the neural stimulation and causes neural plasticity to improve the motor performance.
By increasing the functional activity, their ADL's can be improved to help them in becoming the active member of the society.
Study Type
Interventional
Enrollment (Actual)
28
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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Punjab
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Rawalpindi, Punjab, Pakistan, 46060
- Railway General Hospital
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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
40 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients with sub-acute/ chronic stroke (>3 months)
- Modified Ashworth Ranking Scale 1-3
- Montreal Cognitive Assessment scoring >24-30
Exclusion Criteria:
- Any active pathological condition
- Visual or hearing impairment
- Neurological conditions like Epilepsy, Parkinson, Alzheimer's, Impaired cognition
- Orthopedic issues hindering Mobility Substantially (Fractures, Severe Degenerative Joint Diseases etc.)
- Psychological issues
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mental Imagery with Virtual Reality Group
Mental Imagery with Virtual Reality
|
Mental Imagery TASK Practice with Virtual Reality Training: 30-40 minutes treatment sessions will be performed three times a week for six weeks, Part 1: 2-3 minutes of relaxation Part 2: Visual Imagery (external motor imagery training) for 5-8 minutes Part 3: Actual Task Practice for 10 minutes Part 4: Virtual Reality based training (including games for lower limb functions) for 10 minutes Part 5:Task Oriented training for 10 minutes Tasks for both (mental imagery + actual task practice) will be: Sit-stand task, Static stance (30 seconds), Indoor walk on a leveled surface, Walk indoor towards target, Forward / Side Stepping, Walking outdoors
|
|
Active Comparator: Virtual Reality Alone Group
Virtual Reality Alone
|
Virtual Reality Training: 30-40 minutes treatment sessions will be performed three times a week for six weeks.
Games will include River rush, 20000 water leaks, reflex ridge along with task oriented training.
Tasks will be: Sit-stand task, Static stance (30 seconds), Indoor walk on a leveled surface, Walk indoor towards target, Forward / Side Stepping, Walking outdoors
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fugl Meyer Assessment Scale - Lower Extremity
Time Frame: 6 weeks
|
This scale is recognized as a golden standard for assessment of motor function of stroke patients worldwide.
It focuses on reflex activity, voluntary movements within and outside of synergies, ability to perform isolated movement, and coordination.
Scale items are scored on the basis of ability to complete the item using a 3-point ordinal scale where 0=cannot perform, 1=performs partially and 2=performs fully.
The total possible scale score is 226 Motor score: ranges from 0 (hemiplegia) to 100 points (normal motor performance).
Divided into 66 points for upper extremity and 34 points for the lower extremity.
Sensation: ranges from 0 to 24 points.
Balance: ranges from 0 to 14 points.
Joint range of motion: ranges from 0 to 44 points.
Joint pain: ranges from 0 to 44 points.
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6 weeks
|
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Berg Balance Scale
Time Frame: 6 weeks
|
changes from the baseline, Berg balance scale is used for assessment of balance and fall risk, Higher scores on the berg balance scale indicate greater independence and better ability to balance.
In contrast, lower scores indicate a greater fall risk Items DESCRIPTION SCORE (0-4) Sitting to standing, Standing unsupported, Sitting unsupported, Standing to sitting, Transfers , Standing with eyes closed , Standing with feet together, Reaching forward with outstretched arm, Retrieving object from floor, Turning to look behind, Turning 360 degrees, Placing alternate foot on stool, Standing with one foot in front, Standing on one foot, TOTAL __/56
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6 weeks
|
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Timed Up and Go test
Time Frame: 6 weeks
|
changes from the baseline, Timed up and go test is used for the assessment of falls risk among the elderly population.
The Timed "Up and Go" (TUG) Test measures, in seconds, the time is taken by an individual to stand up from a standard armchair (approximate seat height of 46 cm, arm height 65 cm), walk a distance of 3 meters (approximately 10 feet), turn, walk back to the chair, and sit down.
Normal healthy elderly usually complete the task in 10 seconds or less.
Very frail or weak elderly with poor mobility may take 2 minutes or more.
Clinical guide: <10 seconds = normal <20 seconds = good mobility, can go out alone, mobile without a gait aid <30 seconds = problems, cannot go outside alone, requires a gait aid A score of more than or equal to 14 seconds has been shown to indicate a high risk of falls.
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6 weeks
|
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10-meter walk test
Time Frame: 6 weeks
|
In this test, the participant walks through a 10-m walkway without any break.
At the 4-m of walkway, time is recorded in order to obtain a rhythmic phase of walking speed.
Then the time required over 3 trials was converted to the walking speed.
The reliability of 10-m walk test is 0.83 and literature also shows the construct validity of 10-meter walk test.
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6 weeks
|
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Wisconsin Gait Scale
Time Frame: 6 weeks
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This scale is used to assess gait cycle.
It consists of 14 items, the higher the score, greater will be the disability.
These scale focuses on the components of stance phase, guardedness of affected leg, toe off, swing phase and heel strike.
The reliability of Wisconsin Gait Scale was 0.91 and 0.96 and Cronbach scores were 0.91 and 0.94 respectively.
Minimum score is 13.35 & maximum score is 42.
The higher the score the more seriously affected the gait.
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6 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
April 27, 2022
Primary Completion (Actual)
February 5, 2023
Study Completion (Actual)
February 5, 2023
Study Registration Dates
First Submitted
April 15, 2022
First Submitted That Met QC Criteria
April 15, 2022
First Posted (Actual)
April 21, 2022
Study Record Updates
Last Update Posted (Estimate)
February 21, 2023
Last Update Submitted That Met QC Criteria
February 20, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01261/Tasmiyah Asghar
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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