No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
100 (estimated)
Sponsor
University of Texas at Austin · Other
Who this trial is looking for
This trial is looking for individuals with motor disabilities or able-bodied participants to test brain-controlled devices that help improve movement. Participants will train their brain to use an assistive device while receiving help to enhance their ability to focus.
Are You a Good Fit for This Trial?
You may be able to join if
I have good general health.
I have normal or corrected vision.
I can read and understand English.
I can provide informed consent.
I have motor deficits due to specific conditions like stroke or spinal cord injury.
You may not be able to join if
I have a short attention span or cognitive deficits that prevent me from concentrating during the trial.
I take heavy medication that affects my brain or attention.
I have a serious illness, such as a metabolic disorder.
I have a skin infection, wounds, or dermatitis where the device will be applied.
I have metallic implants that can affect the trial's safety.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Injuries affecting the central nervous system may disrupt the cortical pathways to muscles causing loss of motor control. Nevertheless, the brain still exhibits sensorimotor rhythms (SMRs) during movement intents or motor imagery (MI), which is the mental rehearsal of the kinesthetics of a movement without actually performing it. Brain-computer interfaces (BCIs) can decode SMRs to control assistiv…
Injuries affecting the central nervous system may disrupt the cortical pathways to muscles causing loss of motor control. Nevertheless, the brain still exhibits sensorimotor rhythms (SMRs) during movement intents or motor imagery (MI), which is the mental rehearsal of the kinesthetics of a movement without actually performing it. Brain-computer interfaces (BCIs) can decode SMRs to control assistive devices and promote functional recovery. Despite rapid advancements in non-invasive BCI systems based on EEG, two persistent challenges remain: First, the instability of SMR patterns due to the non-stationarity of neural signals, which may significantly degrade BCI performance over days and hamper the effectiveness of BCI-based rehabilitation. Second, differentiating MI patterns corresponding to fine hand movements of the same limb is still difficult due to the low spatial resolution of EEG. To address the first challenge, subjects usually learn to elicit reliable SMR and improve BCI control through longitudinal training, so a fundamental question is how to accelerate subject training building upon the SMR neurophysiology. In this study, the investigators hypothesize that conditioning the brain with transcutaneous electrical spinal stimulation, which reportedly induces cortical inhibition, would constrain the neural dynamics and promote focal and strong SMR modulations in subsequent MI-based BCI training sessions - leading to accelerated BCI training. To address the second challenge, the investigators hypothesize that neuromuscular electrical stimulation (NMES) applied contingent to the voluntary activation of the primary motor cortex through MI can help differentiate patterns of activity associated with different hand movements of the same limb by consistently recruiting the separate neural pathways associated with each of the movements within a closed-loop BCI setup. The investigators study the neuroplastic changes associated with training with the two stimulation modalities.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Able-bodied participants:
* good general health
* normal or corrected vision
* no history of neurological/psychiatric disease
* ability to read and understand English (Research Personnel do not speak Spanish)
2. Subjects with motor disabilities
* motor defici…
Inclusion Criteria:
1. Able-bodied participants:
* good general health
* normal or corrected vision
* no history of neurological/psychiatric disease
* ability to read and understand English (Research Personnel do not speak Spanish)
2. Subjects with motor disabilities
* motor deficits due to: unilateral and bilateral stroke / spinal cord injury / motor neuron diseases (i.e. amyotrophic lateral sclerosis, spino-cerebellar ataxia, multiple sclerosis) / muscular diseases (i.e. myopathy) / traumatic or neurological pain / movement disorders (i.e. cerebral palsy) / orthopedic / traumatic brain injury / brain tumors
* normal or corrected vision
* ability to read and understand English
* ability to provide informed consent
Exclusion Criteria:
1. Subjects with motor disabilities
* short attentional spans or cognitive deficits that prevent the subject from concentrating during the whole experimental session
* heavy medication affecting the central nervous system (including vigilance)
* concomitant serious illness (e.g., metabolic disorders)
2. All participants
* factors hindering EEG/EMG acquisition and the delivery of non-invasive electrical stimulation (e.g., skin infection, wounds, dermatitis, metal implants under electrodes)
* criteria identified in safety guidelines for MRI and TMS, in particular metallic implants
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