Spinal Cord Injuries Clinical Trial
— NeuroSuitUpOfficial title:
NeuroSuitUp: Neurorehabilitation Through Synergistic Man-machine Intrefaces Promoting Dormant Neuroplasticity in Spinal Cord Injury
NeuroSuitUp is a multidisciplinary neurophysiological & neural rehabilitation engineering project, developed by the Lab of Medical Physics & Digital Innovation, School of Medicine, Faculty of Health Science Aristotle University of Thessaloniki and supported by a Neurosurgical Department. This research is co-financed by Greece and the European Union (European Social Fund- ESF) through the Operational Programme "Human Resources Development, Education and Lifelong Learning 2014- 2020" in the context of the project ""NeuroSuitUp"" (MIS 5047840). The website for the project can be accessed at https://imedphys.med.auth.gr/project/neurosuitup . The investigation's primary objectives include the development, testing and optimization of an intervention based on multiple immersive man-machine interfaces offering rich feedback, that include a) mountable robotic arm controlled with wireless Brain-Computer Interface and b) wearable robotics jacket & gloves in combination with a serious game application and c) augmented reality module for the presentation of the previous two, as well as the development and validation of a self-paced neuro-rehabilitation protocol for patients with Cervical Spinal Cord Injury and the study of cortical activity in chronic spinal cord injury.
Status | Not yet recruiting |
Enrollment | 20 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 14 Years and older |
Eligibility | Inclusion Criteria: - At least 14 yearss of age - clinical diagnosis of Spinal Cord Injury (SCI evaluated by ASIA Impairment Scale) OR Healthy participants (age and gender matched to SCI patients) - Sufficient documentation of the injury in case of patients (neurological examination, MRI scan of the injury level, optional additional CT or x-rays). - Signed informed consent (patients and healthy individuals). Exclusion Criteria: - Other neurological condition that has a possibility to significantly affect the neurological status of the participants (or) the ability to control a BCI (or) the neurophysiological recordings: - Traumatic brain injury - Central Nervous System tumors - Multiple Sclerosis - Amyotrophic Lateral Sclerosis - Parkinson's disease - Refractory Epilepsy - Participation during the last 3months in an another interventional study, the effects of which could affect this study's observations. - Other grave medical condition that could affect the participation (or) the safety of the participants: - Cardiac deficiency - Pulmonary deficiency - Hearing and visual impairments that can affect the participant's understanding of the intervention and performance. - Illegal drug use - Chronic alcoholism |
Country | Name | City | State |
---|---|---|---|
Greece | Laboratory of Medical Physics and Digital Innovation, AUTH | Thessaloniki |
Lead Sponsor | Collaborator |
---|---|
Aristotle University Of Thessaloniki |
Greece,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | BCI control (yes/no) | Ability of participants to modulate brainwave activity in order to achieve control of the BCI. BCI control is evaluated as achieved or not (there are cases of BCI-illiteracy when the participants cannot modulate their brainwaves in order to control the BCI). | Immediately after the intervention | |
Primary | Serious game performance (in-game scoring system) | The ability of participants to control the wearables robotic jacket in order to complete in-game tasks and collect more points. The points will be gather be matching the speed and position of the in-game task instructions while receiving assistance from electrical muscle stimulation. The in-game scoring system uses an accumulative scoring regime according to the correct execution of tasks. There is no upper limit to the score and a higher score means better task execution. Counting starts at 0. | Immediately after the intervention | |
Secondary | Initial Functional Improvement (Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III) | Daily functionality as measured by the Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III).
Score ranges from 0 (min, no functional independence) to 100 (max, fully independent). |
3 months after first participant in first session | |
Secondary | Intermediate Functional Improvement (Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III) | Daily functionality as measured by the Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III).
Score ranges from 0 (min, no functional independence) to 100 (max, fully independent). |
6 months after first participant in first session | |
Secondary | Long-term Functional Improvement (Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III) | Daily functionality as measured by the Greek translation of the Spinal Cord Independence Measure, version III (g-SCIM-III).
Score ranges from 0 (min, no functional independence) to 100 (max, fully independent). |
One year after first participant in first session | |
Secondary | BCI performance classification accuracy | Achieved performance on BCI at conclusion of BCI sessions for each participant. Measured by classification accuracy (percentage of voluntary non-erroneous commands to overall number of detected commands) | 6 months after first participation in first session | |
Secondary | BCI performance by bit rate | Achieved performance on BCI at conclusion of BCI sessions for each participant. Measured by bit rate (number of commands per minute). | 6 months after first participation in first session |
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