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Development of a Brain-controlled Gait Apparatus to restore the walking of people with Spinal Cord Injury

Walk Again Project: development of a Robotic Orthosis Controlled by Biological Signals to restore the ambulation in patients with Spinal Cord Injury - -: -

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-2pb8gq
Enrollment
Unknown
Registered
2019-09-18
Start date
2013-11-04
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

Spinal cord injury sequelae

Interventions

F04.096.628.579
E02.779
G07.568.500
E02.331.800
Gait training with a body weight support system fixed on an ove
Other
A retrospective observational study of the effects of long-term training integrating a non-invasive brain-machine interface (BMI), with visuotactile feedback and locomotion training in 16 individuals
Training with brain-machine control of virtual reality avatar (BMI-VR): During this training, the participants had to imagine moving their legs
the decoded motor intention commanded the walk of an avatar seen in the first person, presented to the participant through a head-mounted display. The brain activity generated from the imagined moveme
F04.754.137.506.662

Sponsors

Associação Alberto Santos Dumont para Apoio à Pesquisa
Lead Sponsor
Associação Alberto Santos Dumont para Apoio à Pesquisa
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 18 years old or over; Lesion T4 to L2; SCI AIS A, B, C or D; Presence of chronic, traumatic, six months to 3 years of SCI.

Exclusion criteria

Exclusion criteria: Has seizures; Has contractures in the legs (shortening of a muscle or tendon); Do not have time for project activities; Participates in other research; Cardiopulmonary instability; Abuse of alcohol or drugs, psychiatric illness, or history of head trauma with loss of consciousness within 3 months of recruitment; Use of drugs known to exert negative effects on motor recovery; Cognitive deficit; Pregnancy or of childbearing potential and not using adequate contraception; Presence of ferromagnetic material in the skull, except in the mouth; Presence of cardiac and/or neural pacemakers; Untreated depression; Spasticity at the lower end of a MAS score equal or higher than 2; Uncontrolled diabetes; Severe osteoporosis; Decubitus ulcer that may interfere with the belt placement or any other necessary feature of the LT BWST-assisted robot and the exoskeleton.

Design outcomes

Primary

MeasureTime frame
EXPECTED: Exoskeleton control by means of the cerebral and muscular electrical activities of the participants, captured non-invasively by EEG/EMG.;OBSERVED: Exoskeleton control by means of the cerebral and muscular electrical activities of the participants captured non-invasively by EEG/EMG. ;OBSERVED: Partial neurological recovery demonstrated as the evolution in the AIS score.

Secondary

MeasureTime frame
EXPECTED: Sensorization of the ICM system through tactile and proprioceptive artificial feedback based on cutaneous space-time stimulation.;EXPECTED: Change in perception of the body schema of the research participants. ;OBSERVED: Sensorization of the BMI system through tactile and proprioceptive artificial feedback based on cutaneous space-time stimulation. ;OBSERVED: Change in perception of the body schema of the research participants. ;OBSERVED: Improvement of cardiovascular, urinary, intestinal and sexual functions, self-esteem and quality of life of the participants.

Countries

Brazil

Contacts

Public ContactAdriana Jorge Ferreira

Associação Alberto Santos Dumont para Apoio à Pesquisa

adriana@aasdap.org.br+5501138721899

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 12, 2026