- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05577013
Kinesio Taping Versus Motor Relearning Program for Upper Limb
Combined Effects of Kinesiotaping and Motor Relearning Program on Upper Limb Motor Function After Stroke
Stroke is described as rapidly developing clinical findings of localized or generalized impairment to cerebral function, with symptoms lasting 24 hours or longer, or leading to death, with no evident cause other than a vascular origin.
Stroke is a prevalent and debilitating illness that affects people all around the world. Stroke is the second or third largest cause of mortality in adults, as well as one of the primary causes of adult disability. Because the majority of stroke patients survive the initial illness, the long-term impacts on patients and their families have the greatest influence on health. Kinesiotaping is a revolutionary rehabilitation procedure. It's most typically used to treat sports injuries, however, it is progressively becoming effective in overcoming other abnormalities. Kinesio Tex tape brand is a flexible, thin, porous cotton fabric with an adhesive backing manufactured by Dr. Kenzo Kase. It provides cutaneous stimulation which facilitates or limit movement, aids in the reduction of edema, reduces pain and correct joint positions for easing muscle spasms.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Rabia shafique, MS NMPT*
- Phone Number: 0345-0386869
- Email: rabiashafiq.kmu@gmail.com
Study Locations
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-
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Peshawar, Pakistan
- Recruiting
- Rehman Medical Institute
-
Contact:
- Rabia Shafique, MS NMPT*
- Phone Number: 03450386869
- Email: rabiashafiq.kmu@gmail.com
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Principal Investigator:
- Rabia Shafique
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- male and female of age 18 -60 years
- patients with post stroke duration of >6 months
- both ischemic and hemorrhagic stroke
- modified ashworth scale of spasticity < 3
- muscle power by manual muscle testing (MMT) ≥ 2
- no cognitive impairments by mini mental state examination (MMSE) > 24
- cortical skin sensitivity preserved (two point discrimination, barognosis, fine and crude touch)
Exclusion Criteria:
- Participants failing to fall in this category would be excluded from the study.
- being hospitalized due to any reason other than stroke
- being subjected to treatment with botulinum toxin for <1 year
- any other condition which affects the upper extremity
- contraindications for the application of Kinesio Taping: open wounds, skin infections such as cellulitis, allergies, skin xerosis
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: (Kinesiotaping and motor relearning program group
The experimental group will receive kinesiotaping; Instructions before applying kinesiotape
|
It will be applied by kinesiotape certified physiotherapist on tendons in the direction of extensor muscle to facilitate range of motion by stretching 50%.
At first it will be applied on extensor pollicis longus and extensor pollicis brevis muscles of hand, extensor digitorum and extensor indicis of last 4 fingers of hand.
Triceps brachii in arm and Supraspinatus and Infraspinatus muscles to stabilize the gelnohumeral joint
|
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Active Comparator: motor relearning program group
The control group will receive motor relearning programme exercises for 40 minutes.
|
Stacking up blocks Stacking up polystyrene cups Folding piece of cloth Using cutlery Pouring water into glass Closing/opening lid of bottles turning the pages of books or newspaper writing on paper Squeezing of ball Coloring in different shapes
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fugel Meyer assessment scale for upper limb
Time Frame: week 8
|
An assessment scale for post stroke hemiplegic patients and is performance-based impairment index.
This scale is having 5 domains namely Motor functioning, Sensory Functioning, Balance, Joint Range of Motion and Joint pain.
I divided the motor functioning for upper extremity into 0 to 66 points and evaluates mobility, speed and coordination
|
week 8
|
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Functionality of Upper Limb
Time Frame: week 8
|
Upper Limb functionality is assessed by an instrument that consists of 20 items divided into 13 items that evaluate the movement patterns of the upper limb with a score from 0 (paralysis) to 5 (performs the typical movement pattern compared to the unaffected side)
|
week 8
|
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Box and Block Test (BBT)
Time Frame: week 8
|
his test is used to evaluate the manual dexterity of post stroke patients.
BBT is composed of wooden box with two equal compartments having 150 boxes in one compartment and patient is asked to move the boxes from one compartment to another within 60 seconds.
Before starting the test an extra 15 seconds time is given to the patient for familiarization with the test.
First the patient performed the activity with the healthy arm and then with the affected arm.
Scoring is done on the basis of the number of boxes transferred from one compartment to another within 60 seconds
|
week 8
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ayesha Afridi, PhD, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC-01043 Rabia
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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