Clinical Trials in Brazil / NCT07768930
Active, not recruiting Not applicable

BCI-Guided Tibialis Anterior FES for Gait Training in Spinal Cord Injury

NCT07768930 · tracked via the Priya Life Science Brazil tracker
Sponsor
Santos Dumont Institute
Phase
Not applicable
Started
2024-11-01
Last updated
2026-08-17

Condition(s) studied

Spinal Cord Injury

Investigational drug(s) / intervention(s)

Ankle Dorsiflexion Rehabilitation

Ankle Dorsiflexion Rehabilitation: The intervention protocol will last 26 min. The first 2 min are used to collect EEG data under baseline conditions, during which the participant does not perform mental tasks or receive electrical stimulation. Then there is 6 min of motor training with Neurofeedback (NFB). During this time, two 10s periods: one in which the FES devices are activated without motor imagery (MI), and another in which the FES is activated by the MI to induce movements in the feet. This includes six separate attempts for the right foot, left foot, and both feet, for a total of 18 attempts. After completing the NFB phase, the participant rests for 6 min to avoid mental and muscular fatigue. Subsequently, the user performs 12 min of training with BCI. This involves 20s intervals of MI to trigger the FES devices to dorsiflex the feet, followed by 20s rest periods. This cycle is repeated for a total of 18 exercises, six for each movement (right foot, left foot and both feet).

Study summary

This study aims to investigate the effectiveness of Brain-Computer Interface (BCI)-guided Functional Electrical Stimulation (FES) in improving muscle activation and gait kinematics in individuals with Spinal Cord Injury (SCI).

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Clinical diagnosis of traumatic spinal cord injury (SCI), classified as AIS grades A to D * Male or female participants * Age between 18 and 60 years Exclusion Criteria: * Skin lesions that preclude the use of functional electrical stimulation (FES) * Lower-limb contractures that preclude the use of FES * Lower-limb spasticity that precludes the use of FES * Osteoporosis * Recent surgical procedure

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Santos Dumont Institute Macaíba Rio Grande do Norte

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07768930 on ClinicalTrials.gov ↗ ← All trials in Brazil