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Study aim
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Evaluating the Effect of Sensory Retraining Exercises on Paresthesia, Balance, Tactile Acuity and Quality of Life in Patients with Multiple Sclerosis
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Design
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A controlled, double group, single blinded (assessor), randomized, phase 3 clinical trial on 30 patients. For randomization permutational randomization method with the number of blocks 5 and block size 6 is used.
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Settings and conduct
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Individuals in both groups are selected from patients with MS who have been referred to centers under the supervision of SUMS. One group will receive sensory retraining exercises and Gabapentin or pregabalin, and another group will receive only drugs. The assessor and the therapist are not the same person, and in this way, the assessor will be blinded.
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Participants/Inclusion and exclusion criteria
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Inclusion criteria: Age over 18 years, Expanded Disability Status Scale less than 6, patient-reported paresthesia symptoms, score of at least 4 out of 10 in at least one of the symptoms of neuropathy on the visual scale in the legs in the past four weeks, balance disorder, no relapse of MS in at least the past 30 days.
Exclusion criteria: Central or peripheral nervous system disorders such as head trauma, stroke, diabetes, Presence of any wounds or swelling at legs, Systemic diseases, pregnancy, lupus, use of tricyclic antidepressant and serotonin and norepinephrine reuptake inhibitors during the study period.
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Intervention groups
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treatment group: participants receive sensory retraining exercises in addition to the drug pregabalin or gabapentin. control group: participants receive pregabalin or gabapentin.
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Main outcome variables
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Paresthesia, Balance, Proprioception, 2-point discrimination, Texture of objects, Quality of life