Robots that learn to interact like humans could transform stroke rehabilitation
NCT ID NCT04578665
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study investigates how people physically interact with each other during tasks like collaboration, competition, and cooperation. The goal is to design robot controllers that mimic these human behaviors, which could then be used in devices like exoskeletons to improve motor learning. The research involves healthy adults, as well as people who have had a stroke or spinal cord injury, and measures changes in movement control and muscle activity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- robotic controllers that mimic human haptic interaction behaviors (collaboration, competition, cooperation)
- What this could lead to
- If successful, this research could lead to more natural and effective robotic exoskeletons or rehabilitation devices that help people recover movement after stroke or spinal cord injury.
- What could go wrong
- This is an early-stage, exploratory study focused on understanding human interaction rather than testing a treatment. The findings may not directly translate into improved rehabilitation outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 764 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2021
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria for Healthy Participants: * Age from 18 to 80 years * No history of a brain and/or skull lesion * Normal hearing and vision, can be corrected * Able to understand and give informed consent * No neurological disorders * Absence of pathology that could cause abnormal movements of extremities (e.g., epilepsy, stroke, marked arthritis, chronic pain, musculoskeletal injuries) * Able to understand and speak English * Height between 3 foot 6 inches (1.1 meters) and 6 foot 2 inches Inclusion Criteria for Participants Post-Stroke: * Age from 18 to 80 years * History of unilateral, supratentorial, ischemic or hemorrhage stroke greater than 6 month * Ability to walk \>10m independently on level ground, allowed to use assistive devices or bracing as needed * Self-selected walking speed is less than 0.8 meters/sec * Medically stable * No concurrent surgeries, medical treatments, participation in research or outpatient therapy * Normal hearing and vision, both can be corrected * Able to understand and give informed consent * Able to understand and speak English * Height between 3 foot 6 inches (1.1 meters) and 6 foot 2 inches Inclusion Criteria for Participants with Spinal Cord Injury: * Age from 18 to 80 years * History of incomplete SCI injury (ASIA C or D) \> 6 months prior * Ability to walk \>10 m independently on level ground, allowed to use assistive devices or bracing as needed * Self-selected walking speed is less than 0.8 meters/sec * Medically stable * No concurrent surgeries, medical treatments, participation in research or outpatient therapy * Normal hearing and vision, both can be corrected * Able to understand and give informed consent * Able to understand and speak English * Height between 3 foot 6 inches (1.1 meters) and 6 foot 2 inches Exclusion Criteria for Healthy Participants: * Weight over 220 lbs * Pregnancy (ruled out by pregnancy questionnaire) * Current presence of wounds or pressure ulcers * Multiple sclerosis, Parkinson's disease or other neurodegenerative disorder, severe dementia, brain injury, spinal cord injury, or cancer of the central nervous system * History of significant head trauma (i.e., extended loss of consciousness, neurological sequelae) * Known structural brain lesion * Significant other disease (heart disease, malignant tumors, mental disorders) * History or peripheral nerve injury * History of sustained non-prescribed drug use or substance abuse (exception: current nicotine use is allowed) * Prior neurosurgical procedures * Inability or unwillingness to perform study-required activities * Prisoners * Unable to meet SRAlab "MRI Pre-Examination Screening Form" requirements Exclusion Criteria for Participants Post-Stroke: * Weight over 220 lbs * Pregnancy (ruled out by pregnancy test) * Botox (botulinum toxin) injection to lower limbs within the prior 3 months, or planned injection during study period. * Current presence of wounds or pressure ulcers * History of sustained non-prescribed drug use or substance abuse (exception: current nicotine use is allowed) * Reduced cognitive function * Severe aphasia * Prisoners * Co-existence of other neurological diseases (e.g., Parkinson's disease or other neurodegenerative disorder, severe dementia, brain injury, spinal cord injury, multiple sclerosis, or cancer of the central nervous system) * History or peripheral nerve injury * Severe hip, knee, or ankle arthritis * Recent fracture or osteoporosis * Significant spasticity in the lower limbs (≥3 on Modified Ashworth Scale) * Medical (cardiac, renal, hepatic, oncological) or psychiatric disease that would interfere with study procedures * Inability or unwillingness to perform study-required activities * Unable to meet SRAlab "MRI Pre-Examination Screening Form" requirements Exclusion Criteria for Participants with Spinal Cord Injury: * Weight over 220 lbs * Pregnancy (ruled out by pregnancy test) * Botox (botulinum toxin) injection to lower limbs within the prior 3 months, or planned injection during study period * Current presence of wounds or pressure ulcers * History of sustained non-prescribed drug use or substance abuse (exception: current nicotine use is allowed) * Prisoners * Co-existence of other neurological diseases (e.g., Parkinson's disease or other neurodegenerative disorder, severe dementia, brain injury, spinal cord injury, multiple sclerosis, or cancer of the central nervous system) * History of peripheral nerve injury * Severe hip, knee, or ankle arthritis * Recent fracture or osteoporosis * Significant spasticity in the lower limbs ( ≥3 on Modified Ashworth Scale) * Medical (cardiac, renal, hepatic, oncological) or psychiatric disease that would interfere with study procedures * Inability or unwillingness to perform study-required activities * Unable to meet SRAlab "MRI Pre-Examination Screening Form" requirements
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Shirley Ryan AbilityLab
Chicago, Illinois, 60611, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Effects of transcranial direct current stimulation and pelvic proprioceptive neuromuscular facilitation on trunk control, balance and functional mobility in stroke patients
- Correlation of visual and motor deficits in stroke patients
- Transcutaneous spinal stimulation with intensive physical therapy for locomotion
- Pilot study on the effects induced by an electromyographic-controlled functional electrical stimulator (FitFES) for upper limb rehabilitation in post-stroke patients
- Early detrusor chemodenervation to preserve bladder compliance and longevity after spinal cord injury
- Brazilian version of a behavior change intervention to support healthy lifestyle adoption after stroke - iVIDAVC: protocol for a pilot randomized study