Robotic Exoskeleton Walking Training After Stroke
Tests a robotic exoskeleton to help walking recovery in adults with stroke.
Plain-language title generated from the registry record
Registry title: Robotic Exoskeleton Assisted Gait Post Stroke
Key facts
- Where
- West Orange, United StatesSee the site
- Phase
- Phase 1
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 21 and 80 years old?
Source: NCT04309305, who can take part
Where in United States
- Kessler FoundationWest Orange, United StatesNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Kessler Foundation
- Trial code
- NCT04309305
- Record updated
- 6 April 2025
- Original description
The current investigation takes advantage of both a progressive and adaptive assist-as-needed massed practice and time-sensitive neuroplasticity through exoskeleton assisted walking in order to induce greater recovery-oriented CNS plasticity and consequent gains in more independent walking.Read full original descriptionShow less
Functional and Neurophysiological Effects of a Progressive Robot Assisted Gait Intervention Early Post Stroke
The current investigation takes advantage of both a progressive and adaptive assist-as-needed massed practice and time-sensitive neuroplasticity through exoskeleton assisted walking in order to induce greater recovery-oriented CNS plasticity and consequent gains in more independent walking.
Inclusion: Stroke survivors < 4 weeks from most recent stroke; Age: 21- 80 years; Unilateral hemiparesis; Medical clearance by the Medical Director; Be able to physically fit into the exoskeleton device; Have joint range of motion within normal functional limits for ambulation; Have sufficient strength to use the hemiwalker, cane or walker (etc. assistive device) while wearing the RE; Patient cognitive status and ability to communicate in English must be at a level consistent with that required to participate in standard motor rehabilitation, e.g. can follow directions; Adequate cognitive function to give informed consent, understand the training, instructions, use investigational devices and give adequate feedback; No history of injury or pathology to the unaffected limb; physically fit within the RE: Height below 60" or above 76" and weight above 220 lbs.
Exclusion: Any metal implants that are NOT MRI-compatible; Pre-existing condition that caused exercise intolerance.(Documented uncontrolled hypertension, coronary artery disease, cardiac arrhythmia, or congestive heart failure); Hospitalization for heart attack, heart surgery or acute heart failure within 3 months of enrollment in study; Severe cognitive or psychiatric problems as well as incontinence might be contraindications to start training with a RE; History of severe cardiac disease such as myocardial infarction, congestive heart failure; Uncontrolled seizure disorder; Neuromuscular or neurological pathologies (e.g., Parkinson's disease, spinal cord injury, or traumatic brain injury with evidence of motor weakness and multiple sclerosis) that will interfere with neuromuscular function, ambulation, or limit the range of motion of the lower limbs; Any medical issue that precludes full weight bearing and ambulation (e.g. orthopedic injuries, pain, severe spasticity); Skin issues that would prevent wearing the device; Uncontrolled spasticity or joint contracture that would interfere with walking in the RE and limits normal ROM during ambulation with assistive devices; Orthopedic pathologies or history that will interfere with ambulation or limit the ROM of the lower limbs (e.g., knee replacement, fixed contractures, inflammation).