Status:

COMPLETED

Functional Magnetic Resonance Imaging (fMRI) and Robot-Assisted Practice of Activities of Daily Living

Lead Sponsor:

Medical College of Wisconsin

Collaborating Sponsors:

National Institutes of Health (NIH)

National Institute of Neurological Disorders and Stroke (NINDS)

Conditions:

Hemiparesis

Ischemic Stroke

Eligibility:

All Genders

30-85 years

Phase:

PHASE1

Brief Summary

The investigators will study motor recovery after robot-assisted therapy after stroke. A small clinical trial will be conducted to quantify the central nervous system changes associated with robotic o...

Detailed Description

Robot-assisted therapy is on the cutting edge of stroke rehabilitation and is a therapy method that promises to improve the lives of persons with disabilities due to stroke. Preliminary studies using ...

Eligibility Criteria

Inclusion

  • Stroke:
  • 30 to 85 years
  • Right-handed (evaluated with handedness survey)
  • suffered a unilateral ischemic stroke in the motor control area, which resulted in hemiparesis of the arm (confirmed by medical data),
  • at least 6-months post-stroke
  • residual movement at least (a) 15 degree shoulder flexion or adduction, (b) 15 degree active elbow flexion and extension
  • not claustrophobic
  • not depressed (as measured depression survey)
  • able to use the scanner, i.e., passes the fMRI screening survey
  • able to understand the instructions and complete the tracking tasks Control
  • older than 20 years
  • Right-handed (evaluated with survey)
  • not claustrophobic
  • able to use the scanner, i.e., passes the fMRI screening survey
  • able to understand the instructions and complete the tracking tasks
  • no history of neurological disorders --not depressed (as measured depression survey)

Exclusion

  • Stroke:
  • brain stem, stroke
  • pre-existing neurological or psychiatric disorders
  • Spasticity \>3 at elbow or fingers on Ashworth
  • demonstrated visuospatial, language or attention deficits of a severity that prevents understanding the task
  • shoulder pain or joint pain during movements
  • synkinetic movements or mirror movements
  • decline to participate
  • will not comply with full protocol
  • pregnant
  • allergic to goretex and conductivity gel
  • Control
  • decline to participate
  • will not comply with full protocol
  • pregnant
  • allergic to goretex and conductivity gel

Key Trial Info

Start Date :

November 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2013

Estimated Enrollment :

61 Patients enrolled

Trial Details

Trial ID

NCT00878085

Start Date

November 1 2008

End Date

June 1 2013

Last Update

February 4 2014

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Medical College of Wisconsin

Milwaukee, Wisconsin, United States, 53226

2

Clement J Zablocki VA

Milwaukee, Wisconsin, United States, 53295