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Recovery of movement after Stroke using combined brain stimulation, interactive technologies and robotic therapy

Analysis of the effects of neuromodulation using Transcranial Alternating Current Stimulation and Transcranial Magnetic Stimulation associated with Motor Imagery therapy, Brain-computer Interface, Functional Electrical Stimulation and Robotic Device in post-stroke rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-8yqgf3c
Enrollment
40
Registered
2026-05-08
Start date
2026-03-25
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stroke Hemiplegia

Interventions

This study is designed as a controlled, randomized, exploratory, and interventional clinical trial. Pilot group: 10 healthy volunteers will participate in the initial phase of the study for validation

Sponsors

Centro de Ciências da Saúde
Lead Sponsor
Centro de Ciências da Saúde
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients of both sexes, aged between 18 and 80 years, with cortical or subcortical Stroke resulting from a single event; presenting upper limb paralysis; with a minimum time of 6 months since Stroke onset; without acute psychiatric or neurological conditions other than Stroke; without cerebellar lesions or bilateral motor deficits; without pregnancy; without claustrophobia; without epilepsy or use of antiepileptic medication within the last 6 months; able to understand and follow instructions

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: autonomic dysreflexia; pressure ulcers; thrombosis; peripheral neuropathy; severe aphasia; severe perceptual problems or other neurological conditions, such as Parkinson’s disease and dementia; history of upper limb surgery within the last 6 months; osteoporotic fractures within the last two years; severe osteoporosis; use of neuroleptic or anticonvulsant medications; skin lesions at the electrode placement site; severely impaired visual ability; history of more than one stroke episode; and refusal to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
It is expected that post-Stroke patients in Groups I and II will demonstrate a faster recovery of ipsilesional corticospinal tract integrity compared with patients in Group III, providing direct evidence related to the modulation of mu and beta rhythms associated with the perilesional motor task

Secondary

MeasureTime frame
Based on the primary results obtained in this study, future investments are intended for the development and application of therapeutic protocols, as well as for the dissemination of the findings to the scientific community, with the aim of enabling the development of new treatment strategies and accelerating upper limb motor rehabilitation in individuals with neuromotor dysfunctions after Stroke

Countries

BR

Contacts

Public ContactFernanda de Souza

Universidade Federal do Espiríto Santo

fernandavaz.souza@hotmail.com+5527999937077

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Jun 11, 2026