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Effect of virtual reality associated with transcranial direct current stimulation to treat trunk control and improve autonomic response in people with spinal cord injury

Phase 1
Recruiting
Conditions
Spinal Cord Injuries
Registration Number
RBR-3zkf2yc
Lead Sponsor
niversidade Federal de São Paulo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

All participants who agree to participate after reading and signing the Free and Informed Consent Term (FICT) will be included; with diagnosis of spinal cord injury - quadriplegic or paraplegic with neurological level equal to or greater than T6; age equal to or greater than 18 years and less than or equal to 60 years and with incomplete injuries.

Exclusion Criteria

Individuals who are not able to perform virtual reality tasks will be excluded; patients with severe heart disease; with metallic implants in the skull; deformities and / or absence of the skullcap; congenital anomalies; patients using drugs that interfere with the ANS (such as antiarrhythmics, insulin, beta-blockers); patients with associated brain injuries that have resulted in significant motor and cognitive deficits and individuals with a convulsive history.

Study & Design

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