Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05106140

Robotic Evaluations of Motor Learning During Stroke Neurorehabilitation

Led by University of Calgary · Updated on 2021-11-03

300

Participants Needed

4

Research Sites

258 weeks

Total Duration

On this page

Sponsors

U

University of Calgary

Lead Sponsor

C

Canadian Institutes of Health Research (CIHR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The RELEARN trial is a a prospective longitudinal cohort study sampled by convenience. Stroke survivors and healthy control individuals will be recruited to analyze motor learning in the upper extremity and its neural basis in early stroke recovery.

CONDITIONS

Official Title

Robotic Evaluations of Motor Learning During Stroke Neurorehabilitation

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Stroke Participants must have a first-time, unilateral ischemic stroke in the middle cerebral artery area confirmed by clinical exam and imaging
  • Be 7 plus or minus 6 days post-stroke
  • Have upper limb impairment
  • Be older than 18 years
  • Have a Fugl-Meyer upper extremity score between 30 and 57
  • Have corrected vision better than 20/50
  • Be able to follow three-step task commands
  • Control Participants must be older than 18 years
  • Control Participants must be in good health
Not Eligible

You will not qualify if you...

  • Stroke Participants with past undiagnosed stroke seen on imaging
  • Stroke Participants with neglect as screened by the Behavioral Inattention Test
  • Stroke Participants with apraxia
  • Stroke Participants with upper extremity orthopedic or muscular issues
  • Stroke Participants with secondary neurologic injury or disease such as Parkinson's
  • Stroke Participants with contraindications to MRI
  • Stroke Participants with medical or neuropsychiatric conditions interfering with study outcomes or posing risk
  • Stroke Participants enrolled in interventional trials supplementing standard therapy
  • Control Participants with significant upper limb neurologic or orthopedic conditions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Carewest Dr. Vernon Fanning Centre

Calgary, Alberta, Canada, T2E 6V7

Actively Recruiting

2

University of Calgary - Kinesiology Building

Calgary, Alberta, Canada, T2N 1N4

Actively Recruiting

3

Foothills Hospital - Main Building

Calgary, Alberta, Canada, T2N2T9

Actively Recruiting

4

University of Calgary - Teaching Research and Wellness (TRW) Building

Calgary, Alberta, Canada, T2N2T9

Actively Recruiting

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Research Team

R

Rachel Stone, BA

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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