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The effects of electrical stimulation on the scalp in painful shoulder post-stroke rehabilitation.

Not Applicable
Recruiting
Conditions
Stroke
Shoulder Pain
C10.228.140.300.775
C10.597.617.133.700
Registration Number
RBR-8f5mny
Lead Sponsor
niversidade Nove de Julho
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Adults over 18 years of age; Diagnosed with chronic stroke and complaint of shoulder pain after stroke for at least six months and be able to understand the commands evaluated by the Mini-exam of the metal state (score> 11).

Exclusion Criteria

Contraindications to the use of non-invasive brain stimulation by metal implants near the application site; case history of seizure or epilepsy; skin infection at the application site; gestation or diagnosis of neoplasia; excessive spasticity with scores greater than 3 indicated by the modified ashworth scale on both elbow, wrist or phalangeal flexors of the affected limb; case history of progressive neurological disease; diagnosis of acute coronary syndrome, patients with severe cardiac events with scores greater than 3 indicated by the New York Heart Association functional classification; frozen shoulder diagnosis; suspicion or confirmation of recent fracture in upper limbs; diagnosis of cancer or in palliative care therapy; recent use of botulinum toxin injection in the upper limb affected in the last 3 months or need for its use during the study period; recent use of phenol injection in affected upper limb in the last 6 months or need for the use during the study period; severe sensory deficits with scores less than 2 indicated by the National Institutes of Health Stroke*; severe aphasia with scores greater than 2 assessed in the native language of the patient indicated by the National Institutes of Health Stroke; severe neglect with scores greater than 2 indicated by the National Institutes of Health's Stroke scale*; use of medications that may interfere with assessments as steroidal anti-inflammatory drugs; individuals who perform physical or homeopathic therapy during the study.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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