Skip to content

Evaluation of Electrical Activity Tibial Muscle and Postural Control of Individuals With Hemiparesia Post TDCS Associated With FES

EVALUATION OF ELECTRICAL ACTIVITY TIBIAL MUSCLE AND POSTURAL CONTROL OF INDIVIDUALS WITH HEMIPARESIA FROM AVE SUBMITTED TDCS ASSOCIATED WITH FES - CLINICAL STUDY, RANDOMIZED, DOUBLE BLIND.

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03008720
Enrollment
2
Registered
2017-01-02
Start date
2017-02-28
Completion date
2018-11-30
Last updated
2017-01-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electromyography, Hemiparesis, Transcranial Direct Current Stimulation

Keywords

functional electrical simulation

Brief summary

Introduction: It is suggested that increased cortical activity, induced by cerebral stimulation associated or not with other rehabilitation techniques, may potentiate the motor and functional therapeutic effects in individuals with neurological deficits. Objectives: To evaluate the electrical activity of the anterior tibial muscle (TA) and postural control of individuals with hemiparesis due to stroke following treatment with transcranial direct current (tDCS) stimulation and functional electrical stimulation (FES), associated or isolated). (EMG) and postural control by the Balance Evaluation Systems Test (BESTest). Both of which were collected at four different time points: pre-treatment, immediately after 10 treatment sessions, and 30 days follow-up after the interventions. Patients will be randomized into 4 experimental groups: tDCS anodic active + active FES+ active contraction TA, tDCS sham + active FES+ active contraction TA, tDCS anodic active+ placebo FES+ active contraction TA, tDCS sham+ FES sham+ active contraction TA. tDCS (2mA) will be applied over the motor (Cz) and cathodic vertex over the supraorbital region of the normal hemisphere and FES over hemiparetic TA by a researcher who will not be the one who will evaluate the anesthesia patient. The treatment will last 10 sessions, twice a week, with a time of 20 minutes.

Interventions

DEVICETranscranial direct current stimulation (tDCS)
DEVICESham stimulation

Sponsors

University of Nove de Julho
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Months to No maximum
Healthy volunteers
No

Inclusion criteria

* Individuals with hemiparesis due to stroke; * Both sexes; * Agree to sign the free and informed consent form.

Exclusion criteria

* Positive cut-off point for the Mini Mental State Examination (MMSE) of less than 11 points already corrected for schooling; * Ankle mobility reduced by history of fracture or use of ankle fasteners; * Irreducible equine deformity; * Muscle strength level of AT less than 1 by the scale of Kendall; * Patients with reported severe visual impairment; * Contraindications to the use of transcranial direct current stimulation (history of seizure or recurrent epilepsy, brain tumors at the stimulation site, metallic materials implanted in the brain); * Individuals with cutaneous infection at the point of application of FECC or FES; * Individuals who presented anesthesia or hyperesthesia at the point of application of the ECTS; * Individuals diagnosed with deep venous thrombosis (DVT); * Individuals diagnosed with degenerative diseases or polyneuropathies. * Individuals who do not present complementary tests that diagnose the lesion site.

Design outcomes

Primary

MeasureTime frame
electrical activity (median frequency and amplitude of the electromyographic signal) of the anterior tibial muscle1 YEAR

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026