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A clinical study of non-invasive brain stimulation in unilateral spatial neglect after stroke

Effect of transcranial electric stimulation in unilateral spatial neglect after Stroke - ELETRON Trial Effect of transcraniaL ElecTRic stimulatiON in unilateral spatial neglect after Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-78jvzx
Enrollment
Unknown
Registered
2016-05-03
Start date
2017-04-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Stroke, hemiplegia

Interventions

A direct current was delivered by a battery-powered device (DC-Stimulator Plus model, NeuroConn, neuroCare Group GmbH, München, Germany) using two pairs of surface saline-soaked sponge electrodes (5 c
E02.331.750

Sponsors

Hospital das Clínicas da Faculdade de Medicina de Botucatu
Lead Sponsor
Universidade de São Paulo
Collaborator
Faculdade de Medicina de Ribeirão Preto/Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients will eligible for inclusion in the trial if they will aged at least 18 years and had USN after ischemic stroke diagnosis within six months of the start of stroke symptoms (subacute phase). Ischemic stroke will be confirm using computed tomography (CT) or magnetic resonance imaging (MRI), and USN will objectively diagnosed using conventional Behavior Inattention Tasks (BIT-C) with a cutoff value of <129.

Exclusion criteria

Exclusion criteria: Individuals will excluded if they will suffer hemorrhagic stroke, metal-in-cranium injuries near the electrode placement area, intracerebral vascular clips or any other electrically sensitive support system, clinical instability, epilepsy, severe cognitive impairment, bilateral lesions, global aphasia, previous visual disturbances, pregnancy, or other neurological diseases.

Design outcomes

Primary

MeasureTime frame
Decrease the degree of unilateral spatial neglect after treatment verified by Behavior Inattention Test (BIT), from finding a variation of at least 15% in the pre and post intervention measurements

Secondary

MeasureTime frame
Decrease the degree of unilateral spatial neglect after treatment verified by Catherine Bergego scale, from finding a variation of at least 15% in the pre and post intervention measurements;Increasing the degree of autonomy observed with the Barthel indez, from the finding of a change of at least 15% in pre and post intervention measurements.;Increasing the degree of quality of life observed with the European (5D) Quality of life Scale, from the finding of a change of at least 15% in pre and post intervention measurements.;Decrease of stroke severity observed with the National Institutes of Health Stroke Scale (NIHSS), from the finding of a change of at least 15% in pre and post intervention measurements.;Increasing the degree of functional impairment observed with the Functional Independence Measure (FIM), from the finding of a change of at least 15% in pre and post intervention measurements.

Countries

Brazil

Contacts

Public ContactGustavo Luvizutto

Hospital das Clínicas da Faculdade de Medicina de Botucatu

gluvizutto@gmail.com+55(14)981157727

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 1, 2026