Actively Recruiting

Early Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
ID06656754

Error-enhanced Learning and Recovery in 3D Isometric Movement Training for Stroke and Healthy Adults

Led by Shirley Ryan AbilityLab · Updated on 2025-01-09

56

Participants Needed

1

Research Sites

232 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying the effects of 3D isometric movement training in both healthy adults and adults who have impairments due to stroke. The trial aims to understand how movement skills can be trained when sensory inputs like proprioception are changed, using a three-dimensional environment. This early phase 1 study builds on previous findings in two-dimensional settings and applies these techniques to neurotypical adults and stroke survivors to compare their movement errors during different reaching tasks. Participants will use a robotic arm in a 3D visual display system to perform targeted reaching tasks. First, they will do unconstrained reaching, followed by isometric reaching where the robotic arm is fixed, and their applied forces move a simulated arm on the screen. Visual feedback is provided through a virtual avatar of their arm. The study measures the perpendicular error, which is the difference between the ideal and actual reaching paths, to compare performance under unconstrained and constrained conditions. During the study, participants will practice reaching tasks while researchers monitor their movement accuracy using the virtual reality system and robotic arm. Assessments include visual tests and cognitive screenings to ensure participants can complete the tasks. The main outcome measured is the average perpendicular error over about one year. Safety measures such as blood pressure and oxygen levels will be monitored. Participants may be followed throughout the one-year study period to observe changes in their movement performance.

CONDITIONS

Official Title

R01.Aim 2.Study 1: IsoReach

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Neurotypical participants must be 18 years old or older
  • No history of stroke for neurotypical participants
  • Ability to provide informed consent for neurotypical participants
  • Stroke participants must be 18 years old or older
  • Stroke participants must have chronic stroke (8+ months post-stroke)
  • Stroke participants must have available medical records and imaging about lesion locations
  • Stroke participants must have hemiparesis with primary motor cortex involvement
  • Stroke participants must have some shoulder and elbow movement capability
Not Eligible

You will not qualify if you...

  • Neurotypical participants with severe medical problems including cardiovascular, orthopedic, or neurological conditions
  • Neurotypical participants with medical problems affecting movement, range of motion, strength, or coordination of upper limbs
  • Neurotypical participants with visual deficits affecting task performance (visual field deficits worse than 20/100, poor depth perception below specified thresholds)
  • Neurotypical participants with blood pressure above 140/90 mmHg
  • Neurotypical participants with blood oxygen less than 92%
  • Stroke participants with bilateral paresis
  • Stroke participants with aphasia, cognitive impairment, or affective dysfunction preventing task performance (based on Mini Mental State Examination scores adjusted for education)
  • Stroke participants with visual deficits and hemispatial neglect preventing target seeing (assessed by visual field loss, visual extinction, and depth perception tests)
  • Stroke participants with Modified Ashworth score of 4 at shoulder or elbow joints
  • Stroke participants scoring below 15 on FMUE scale
  • Stroke participants unable to provide informed consent
  • Stroke participants with severe current medical problems
  • Stroke participants with severe sensory deficit in the affected upper limb
  • Stroke participants with diffuse/multiple lesion sites or multiple stroke events
  • Stroke participants unable to maintain testing positions
  • Stroke participants who received botulinum toxin injection to affected upper limb within previous 4 months
  • Stroke participants currently in upper extremity rehabilitation therapy or research intervention
  • Stroke participants with neurological, neuromuscular, or orthopedic diseases affecting the affected arm or hand
  • Stroke participants with other neurological conditions such as Parkinson's or cerebral palsy
  • Stroke participants with blood pressure above 140/90 mmHg
  • Stroke participants with blood oxygen less than 92% on finger pulse oximetry testing

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Shirley Ryan AbilityLab

Chicago, Illinois, United States, 60611

Actively Recruiting

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Research Team

A

Arturo Ramirez

C

Courtney Celian, OTR/L

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

Frequently Asked Questions

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