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Clinical Trials/NCT01298583
NCT01298583
Completed
Phase 1

Ankle Tracking Training in Stroke

University of Minnesota1 site in 1 country16 target enrollmentJanuary 2007
ConditionsStroke

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Stroke
Sponsor
University of Minnesota
Enrollment
16
Locations
1
Primary Endpoint
ankle range of motion
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to compare the improvement in ankle control and brain activation in subjects with stroke resulting from two different forms of telerehabilitation: tracking training, emphasizing accurate movements, versus movement training, involving simple movements.

Hypotheses:

  1. The Track group will show greater improvement in ankle range of motion compared to the Move group.
  2. The Track group will show greater improvement in ankle tracking accuracy and greater changes in fMRI (increase in relative volume of activation for ipsilesional sensorimotor cortex, increase in laterality index, and decrease in blood-oxygen-level-dependent (BOLD) signal intensity index) compared to Move group.
  3. The Track group will show greater improvement in tracking accuracy at an untrained joint (knee) compared to the Move group.
  4. The Track group will show greater improvement in standing balance.
  5. The Track group will show greater improvement in walking speed and ankle dorsiflexion during gait compared to the Move group.
Registry
clinicaltrials.gov
Start Date
January 2007
End Date
December 2010
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Single stroke with an ischemic infarct.
  • Between 18 and 85 years of age.
  • Time since stroke onset must be \>6 months.
  • Cannot be receiving any rehabilitation therapy.
  • Impaired ankle dorsiflexion/plantarflexion but at least 10 degrees of active motion.
  • Cognition level must be at least 24 out of 30 on the Mini-Mental Examination
  • Able to ambulate at least 100 feet independently. training.

Exclusion Criteria

  • Cannot have any neuromuscular disorder other than stroke that impairs ankle motion.
  • Cannot have an executive function score on Stroop Interference Test of \<
  • Cannot have a score on the Beck Depression Inventory of \>
  • Cannot have ataxia, apraxia, receptive aphasia, hemi-neglect, or severe visual field cut .
  • Cannot be pregnant nor have indwelling metal or medical devices incompatible with fMRI.

Outcomes

Primary Outcomes

ankle range of motion

Time Frame: Measurement at pretest, posttest and followup

Study Sites (1)

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