- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06680063
Correlation Between Clinical Assessment and Neurophysiological Assessment in Spinal Cord Injury
Study Overview
Status
Detailed Description
Spinal cord injury (SCI) cause disruption of descending control pathway in spinal cord. The disruption of descending control induce impaired motor and sensory function below the level of injury, as well as the electrical signal from supraspinal pathway. During spinal shock phase, spinal motoneuron become hypoexcitability, as resulting in muscle hypotonicity or flaccidity in clinical manifestation. The spinal motoneuron gradually increase during sub-acute to chronic phase as resulting in development of spasticity in SCI. Development of spasticity is realted to increase of spinal motoneuron excitability, which shown in a decrease in H-reflex latency and increase in Hmax/Mmax ratio. A previous study shown a medium correlation between Hmax/Mmax ratio and MAS in SCI and stroke people. Moreover, the MAS shown a strong correlation with Fugle-meyer score in stroke people. However, it remains unclear in correlation between clinical outcome and neurophysiological outcome assessment of spasticity, and the correlation of spasticity and the motor function in SCI.
This study aims to explore the correlation between clinical assessment and neurophysiological assessment of spasticity in SCI.The clinical outcome assessment are modified-Modified Ashworth scale (m-MAS) and lower extremity motor score (LEMS). The lower extremity motor score is obtained from American Spinal Injury Association (ASIA) imapirement scale. The neurophysiological outcome assessment is H-reflex methode. All particiants who will participated into this study will be assessed the m-MAS, LEMS and H-reflex.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Salaya
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Nakhon Pathom, Salaya, Thailand, 73170
- Mahidol University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals with any level of SCI with age between 18-70 years.
- Onset of injury between 1-30 month.
- Presentation of H-reflex.
Exclusion Criteria:
- Having history of other neurological disease e.g. stroke
- Absent of H-reflex.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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modified-Modified Ashworth scale
Time Frame: 1 day
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The modified-Modified Ashworth scale is a clinical outcome to evaluate level of spasticity in neurological patient.
The MAS consists of 6 grading scale, range from 0 to 5; (i) 0: no increase in muscle tone or normal, (ii) 1: slight increase in muscle tone, with a cathch and release or minimal resistance at the end of the range of motion, (iii) 4: slight increase in muscle tone, manifested as a cathch, followed by minimal resistance through the remainder (less than half) of the range of motion, (iv) 3: a marked increase in muscle tone throughout most of the range of motion, but affected parts still easily moved, (v) 4: considered increase in muscle tone, passive movement difficult, (vi) 4: affected parts rigid in flexion or extension.
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1 day
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Lower extremity motor score
Time Frame: 1 day
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The lower extremity motor score (LEMS) is obtained from American Spinal Injury Association (ASIA) imapirment scale.
The ASIA imapirment scale consists of motor, sensory and anorectal examination.
This assessment is an standard assessment form for SCI.
The lower extremity motor score assess 5 key lower extremity muscles.
which are hip flexors, knee extensors, ankle plantar flexors, ankle dorsiflexors and long toe extensors.
These 5 key muscles represent motor recovery throughout myotome of the body.
Grading of this assessment range from 0 to 5, according to mannual muscle testing grading system.
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1 day
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Soleus H-reflex
Time Frame: 1 day
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A most reliable are for assess spinal motoneuron excitability is soleus H-reflex.
The stimulation electrode place over the popletial fossa to stimulate tibial nerve.
Two disposal surface electrode place over 1/3 of lower leg which is over the soleus muscle.
Data from the assessment are H-reflex latency, H-reflex amplitude, M-wave response amplitude.
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1 day
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neurologic Manifestations
- Musculoskeletal Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Muscular Diseases
- Muscle Hypertonia
- Neuromuscular Manifestations
- Trauma, Nervous System
- Spinal Cord Diseases
- Paralysis
- Muscle Spasticity
- Wounds and Injuries
- Spinal Cord Injuries
- Quadriplegia
- Paraplegia
Other Study ID Numbers
- MU-CIRB 2023/119.0504-1
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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