Transcutaneous Direct Current Stimulation of the Spinal Cord for Treatment of Spasticity in Multiple Sclerosis

Not Applicable

• Conditions: Spastic Parapareses
• Interventions: Device: Transcutaneous Spinal Direct Current Stimulation

• Registration Number: NCT04287244
• Lead Sponsor: Lebanese American University

Brief Summary

The current research is aimed at using Transcutaneous Spinal Direct Current Stimulation (tSDCS) as complementary therapeutic tool in the treatment of spasticity in multiple sclerosis. Patients will be randomized into two groups (tSDCS-anode vs. tSDCS-sham) according to the detailed protocol. Main outcome will be measured by the change in walking speed using the Timed 25-Foot Walk (T25FW).

A total of 40 patients ought to be enrolled as specified in methodology. Secondary outcomes will assess functional improvement through Multiple Sclerosis Walking Scale (MSWS) Short Form - 36 (SF-36), Expanded Disability Status Scale (EDSS) and Ashworth scale.

Detailed Description

Spasticity is experienced in around 80 % of patients with multiple sclerosis resulting in quality of life impairment. Transcranial direct current stimulation has been proven effective for the treatment of spasticity in patients with chronic stroke or cerebral palsy. The effect of transcutaneous spinal direct current stimulation (tSDCS) has been applied in spasticity but not in patients with spasticity due to multiple sclerosis. The study aims to assess the efficacy of anodal tSDCS on spasticity in multiple sclerosis patients through several assessment tools. The investigators hypothesize that anodal tSDCS will reduce spasticity in multiple sclerosis patients.

The study will be double blind sham-controlled crossover. The patients will be examined by the described assessment tools (T25FW, MSWS, SF-36, Ashworth, EDSS) before receiving tSDCS. The sessions of tSDCS will be applied 1 session per day in 5 consecutive days. Assessment using the scales and questionnaires will be performed at the end of the 5 days of stimulation, 1 week after the last day of first block of sessions and 2 weeks later. The group will be crossed and another block of 5 consecutive days of stimulation will follow. Assessment will take place again on first day and last day of the stimulations followed as well by assessment 1 week after the last day of second block of stimulation and 2 weeks after.

Study Timeline

• Study First Submitted: 2020-02-19
• Study First Submitted QC: 2020-02-26
• Study First Posted: 2020-02-27
• Status Verified: 2020-03
• Study Start: 2020-03
• Last Update Submitted: 2020-03-03
• Last Update Posted: 2020-03-04
• Primary Completion: 2022-02
• Study Completion: 2022-05

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

-Patients diagnosed with Multiple Sclerosis according to the 2010 Mc Donald criteria with spasticity in the lower extremities

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Exclusion Criteria

• Cardiac pacemakers
• Patients with prior exposure to tDCS
• Metallic hardware in the spine
• Eczema or skin abrasion at the intended site of stimulation
• Currently pregnant or plan for pregnancy in the next 6 months
• Heart or respiratory failure resulting in activity impairment
• Walking impairment due to orthopaedics condition such as deformity or recent fracture.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Active tSDCS	Transcutaneous Spinal Direct Current Stimulation	Anodal tSDCS will be administered through a pair of conductive rubber electrodes covered by saline soaked sponges (35 cm2). The current will be delivered continuously at 2 mA for 30 min through a battery-driven constant-current stimulator (designed by Sooma). The anode will be positioned over the spinal cord area at the level of the spinous processes of 10th-11th thoracic vertebra.
Sham tSDCS	Transcutaneous Spinal Direct Current Stimulation	Sham stimulation will be delivered to the same spinal cord area using a sham tSDCS device that delivers a direct current for 10 seconds at the beginning and end of tSDCS to provide sensory experiences similar to active stimulation.

Primary Outcome Measures

Name	Time	Method
Gait improvement	5 days	The primary objective of the study is to achieve 20% gait speed improvement on 25 feet walking test (T25WT) after spasticity reduction by cathodal tSDCS.

Secondary Outcome Measures

Name	Time	Method
Multiple Sclerosis Walking Assessment	19 days	Using Multiple Sclerosis Walking Scale (0-12)
Quality of Life Measures	19 days	Assessed through Short Form - 36 (0-100)
Disability Measure	19 days	Through Extended Disability Status Scale (0-10)
Spasticity Assessment	19 days	Assessment by Ashworth scale (0-4)