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A Multi-site, Interventional, Non-comparative, single-arm trial to evaluate the safety of the ReWalk Restore Device in Subjects with Mobility Impairments Due to Ischemic or Hemorrhagic Stroke

This project will assess the safety of the Restore device during gait rehabilitation activities in post-stroke individuals undergoing physical therapy. It will also evaluate the use of the Restore device during common assessment methodologies occurring during physical therapy activities.
Duration

Seven 2-3 hour visits for 4 weeks.

Inclusion Criteria
  • Had a stroke more than 2 weeks ago.
  • At least 18 years old.
  • Between 4'8" and 6'7" tall.
  • Weigh less than 264 lbs.
  • Speak English.
  • Have weakness on one side of body.
  • Able to walk at least 5 feet (with assistance if needed) without ankle foot orthosis, if participant wears one.
  • Able to follow multi-step directions and commands, as determined by a member of the study team.
  • Able to physically fit into the components of the robotic device.
  • Have normal motion of limbs to walk safely, as determined by a member of the study team. 
  • Willing and able to give informed consent.
Compensation

None.

Research Categories
Stroke
Actively Recruiting
No