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Combined Electrical Stimulation of the Brain and Muscles for patients with Spinal Cord Injury: an experimental study

Not Applicable
Conditions
Spinal Cord Diseases
Registration Number
RBR-7w3jw35
Lead Sponsor
niversidade Estadual de Campinas
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Spinal cord injury at any neurological level from C2 to T12 for at least one year. Stable neurological deficit for at least 6 months. Over 18 years of age. Both sexes. Pain at the neurological level of injury or below with a Neuropathic Pain 4 (DN4) scale equal to or greater than 4

Exclusion Criteria

Cognitive impairment that prevents the safe completion of electrode training. Neuropathic pain prior to spinal cord injury. Other chronic pain syndromes, especially fibromyalgia and complex regional pain syndrome. Extensive skin lesions that do not allow electrode coupling. Decompensated mood disorder. Epilepsy. Use of a pacemaker

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It is expected to observe improvement in chronic pain, as assessed by the Neuropathic Pain Symptoms Inventory (NPSI), McGill Pain Questionnaire (MPQ), and Pain Quality Assessment Questionnaire (PQAS), with a minimum variation of 5% between pre- and post-intervention measurements
Secondary Outcome Measures
NameTimeMethod
It is expected to observe improvement in quality of life, as assessed by the Short-form Health Survey-36 (SF-36) and Quality of Life Index Spinal Cord Injury III (QoLSCI), with a minimum variation of 5% between pre- and post-intervention measurements;It is expected to observe an increase in muscle strength, as assessed by the peak isometric force, with a minimum variation of 5% between pre- and post-intervention measurements;It is expected to observe a lowering of the level of sensory injury, as assessed by the American Spinal Cord Injury Association Impairment Scale (AIS), with a reduction of at least one sensory dermatome between pre- and post-intervention measurements
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