- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06059755
Mirror Therapy vs Cross Education Non Paretic Limb Training on Strength and Hand Dexterity in Stroke Survivors.
Comparison of Mirror Therapy Versus Cross- Education Non Paretic Limb Training on Upper Limb Strength and Hand Dexterity in Stroke Survivors.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A stroke or CVA is characterized by the sudden onset of focal neurological dysfunction symptoms that persist for more than 24 hours (or cause death earlier) and are brought on by an acute vascular injury to a specific area of the brain. Overall, a stroke creates a blockage in the delivery of blood and oxygen to a particular region of the brain, which results in cell death, long-term or lifelong impairments, or even death. Issues with paralysis, motor control, pain-related sensory problems, language usage or comprehension, thinking, memory, and emotional challenges are just a few examples of disabilities.
Stroke can be ischemic or hemorrhagic. Over 100 diseases are associated with ischemic stroke, making it heterogeneous. It is the most common type of stroke and accounts for 87% of all strokes. Ischemic stroke is further divided into two groups; thrombotic stroke (the formation of clot or plaque in blood vessels within the brain) and embolic stroke (the formation of clot or plaque somewhere else in the body and travels to blood vessel of the brain through blood stream).
Atherosclerosis, arterial dissection, and artery-to-artery embolism are all examples of large vessel disease. The primary small vessel diseases causing lacunar strokes are lipohyalinosis and atherosclerosis. Intracerebral hemorrhage, which can occur deep (basal ganglia, brainstem), cerebellum, or lobar, accounts for about 15% of strokes. About 20% of intracerebral hemorrhages are brought on by macro vascular lesions (vascular malformations, aneurysms, cavernomas), venous sinus thrombosis, or other uncommon causes; these are particularly significant in young patients.
Literature review A systematic and evidence based search of relevant literature was performed by utilizing PubMed and Google Scholar as search engines. Search term for the initial literature review was post-stroke mirror therapy, post-stroke cross education, comparison of mirror therapy versus cross education non paretic limb training, upper limb strength and hand dexterity.
O. van der Groen et al. (2023) studied the Corticospinal and intracortical responses from both motor cortices following unilateral concentric versus eccentric contractions and compared responses to transcranial magnetic stimulation(TMS) in both motor cortices following single sessions of unilateral ECC and CON exercise of the elbow flexor and concluded that These findings suggest that responses after a single bout of exercise may not reflect longer term adaptations.
S. Karamat et al. (2022) compared the effects of task-based mirror therapy and Repetitive Facilitation Exercise on upper limb function in post stroke patient. The study concluded that mirror therapy and repetitive facilitation Exercise both were found to be effective in improving upper limb motor functions of acute stroke patients. However, Mirror therapy has shown significant effects in upper extremity functional index.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Tehreem Mukhtar, PhD*
- Phone Number: +923134715275
- Email: tehreem.mukhtar@riphah.edu.pk
Study Locations
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Punjab
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Lahore, Punjab, Pakistan, 54000
- Recruiting
- Tehreem Mukhtar
-
Contact:
- Tehreem Mukhtar, PhD
- Phone Number: +923134715275
- Email: tehreem.mukhtar@riphah.edu.pk
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Age range between 45-65 years.
- Both male and female genders.
- Clinically diagnosed of stroke referred by Neuro physician.
- Patients in the subacute stage, duration of 3 to 6 months from onset.
- Patients with anterior cerebral artery (ACA) and middle cerebral artery (MCA) involvement with the affected side being the dominant side.
- Patients with Mini-Mental State Examination (MMSE) score more than 16.
- According to Modified Ashworth Scale, patients in range of 1 and 1+ (Flexor carpal radialis muscle,Flexor carpal ulnaris muscle, Flexor digitorum profundus muscle, Flexor digitorum superficialis muscle, Flexor pollicis longus muscle, Palmaris longus muscle) will be included .
- Hemiparesis or hemiplegic due to Ischemic stroke
Exclusion Criteria:
- Patients with Alzheimer disease, Parkinson's disease, Multiple sclerosis and Brain tumors .
- Those with severe cognitive impairment , those who were unable to provide informed consent. Patients having acute pericarditis, lumbar puncture within 7 days, Major surgery or major trauma within 14 days.
- Patient with recurrent stroke.
- With unilateral neglect or apraxia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group A: Cross education
For strength training resistance exercises with a load of 60% of one repetition maximum will be performed targeting the muscles involved in upper limb function.
It includes exercises like shoulder presses, wrist curls, elbow flexion, and triceps extensions.
Among the functional movements that are the focus of motor skill training activities for non-paretic limbs are reaching, gripping, and object manipulation.
Patient will be encouraged to mentally visualize themselves performing movements and tasks with the affected limb, while actively engaging the non-paretic limb.
Strength will be measured using the grip strength test/ hand held dynamometer.
Patients will undergo 45-minute session per day, 3 days per week for 6 weeks.
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For strength training resistance exercises with a load of 60% of one repetition maximum will be performed targeting the muscle involved in upper limb function.
Strength will be measured using the grip strength test/hand held dynamometer.
Patients will undergo 45 minute session per day, 3 days per week for 6 weeks.
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|
Experimental: Group B: Mirror Therapy
Participants will be asked to sit in front of a table of appropriate height with their arms resting on the table and a mirror (35 cm × 35 cm) placed between the patient's arms.
The non-affected arm will be placed in front of the mirror and the affected arm will be placed and obscured.
Patient will engage in specific exercises or movements using the affected limb while observing the mirror reflection.
The movements will consist of forearm rotation, elbow, wrist, and finger flexion and extension movements, and hand grasping.
Appropriate movement tasks will be selected according to the function of the affected upper limb.
This exercise will be performed 45 minutes per day, 3 times per week for 6 weeks.
|
Participants will be asked to sit in front of a table of appropriate height with their arms resting on the table and a mirror (35 cm × 35 cm) placed between the patient's arms.
The non-affected arm will be placed in front of the mirror and the affected arm will be placed and obscured.
Appropriate movement tasks will be selected according to the function of the affected upper limb.
This exercise will be performed 45 minutes per day, 3 times per week for 6 weeks
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Action Research Arm Test (For Functional Limitation)
Time Frame: Changes from baseline Action Research Arm Test at 3rd week and after 6 weeks
|
The instrument contains 19 items grouped into 4 subtests; grasp, grip, pinch, and gross motor.
Item performance is rated on a 4-point scale (0=unable; 1=partial; 2= abnormal; 3=normal) then item ratings are summed and reported out of 57 points with higher score indicating greater UE function.
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Changes from baseline Action Research Arm Test at 3rd week and after 6 weeks
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Fugl-Meyer Assessment. (For Upper extremity function)
Time Frame: Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
|
The Fugl-Meyer Assessment is the gold standard to assess motor function of post-stroke hemiparesis.
The FMA-UE consists of 30 items assessing motor function and 3 items assessing reflex function.
The scores most applicable to task performance is given from "0, inability," "1, beginning ability," to "2, normal" (total score range, 0-66).Higher the score more is the independence.
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Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
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Hand-held dynamometer. (For Upper Limb strength assessment)
Time Frame: Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
|
This instrument is scored using force produced in kilograms (0-90) or pounds (0-200).
The subject is seated with back, pelvis and knees as close to 90 degrees as possible, shoulder is adducted and neutrally rotated, elbow flexed to 90 degrees, and forearm neutral and wrist held between 0-15 degrees of ulnar deviation.
Maximum grip is the mean of 3 trails.
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Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
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Stroke Impact Scale (For hand function)
Time Frame: Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
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The Stroke Impact Scale (SIS) is a stroke-specific, self-report, health status measure.
It contains 59 items and assesses 8 domains: Strength - 4 items, Hand function - 5 items, ADL/IADL - 10 items, Mobility - 9 items, Communication - 7 items, Emotion - 9 items, Memory and thinking - 7 items, Participation/Role function - 8 items.
For each item individual is asked to rate the level of difficulty in past two weeks using the scale;1= extremely difficult, 2= very difficult, 3= somewhat difficult, 4= a little difficult, 5= not difficult at all.
On a scale of 0 to 100, with 100 representing full recovery and 0 representing no recovery.
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Changes from baseline Fugl-Meyer Assessment at 3rd week and after 6 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Kianat Rashid, MSPT-NM, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RiphahIU Kainat Rashid
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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