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Action Selection and Arm Rehabilitation After Stroke

Not Applicable
Completed
Conditions
Stroke
Interventions
Behavioral: Arm Training with Action Selection
Registration Number
NCT02785419
Lead Sponsor
University of South Carolina
Brief Summary

After stroke, individuals often have persistent difficulty using the arm and hand in everyday functional tasks that reduces quality of life. Currently available rehabilitation techniques are not adequate and new protocols are needed that are based on an understanding of how brain regions work together to produce skilled movement. This research project aims to improve our understanding of how the brain controls movement after stroke and determine whether a period of motor practice that targets specific brain regions through the addition of action selection demands leads to improved arm function. We hypothesize that arm motor function and the ability to efficiently activate the action selection motor circuit during movement will improve after training.

Detailed Description

Rehabilitation of arm impairment after stroke includes the repetitive practice of functional tasks. In healthy adults, planning plays a vital role in the control of skilled movement, however, the behavioral and neural correlates of planning have largely been unexplored in individuals recovering from stroke. Action selection is an important motor planning process that engages dorsal premotor cortex (PMd) in controls. While PMd activation is a commonly reported neural correlate of motor recovery after stroke, the role of PMd in action selection and motor training are not known. Therefore, the purpose of this study is to determine the effect of training that includes action selection demands on the behavioral and neural correlates of movement after stroke. Thirty-eight individuals in the chronic phase of stroke will be recruited. After completion of clinical measures of impairment and function, all participants with stroke will complete a motor action selection task and functional MRI followed by arm training. Arm training will consist of three weeks (15 sessions) of arm motor training (1.5 hours per session) that includes action selection demands on movement. Follow-up clinical testing will occur at the end of treatment and three weeks later.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • At least 18 years old
  • Had stroke at least 6 months ago
  • Right-hand dominant prior to stroke
  • Some continued arm and hand weakness
  • Some ability to move the arm and hand that is weaker from the stroke
Exclusion Criteria
  • Acute medical issues that would interfere with participation
  • Another neurologic diagnosis that may impact movement (e.g. Parkinson's Disease)
  • Cannot undergo MRI scanning
  • Severe apraxia or hemispatial neglect
  • Pain in the arm that interferes with movement
  • Difficulty maintaining attention or following directions

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Arm Training with Action SelectionArm Training with Action SelectionTask-oriented, functional arm training with the addition of action selection cues to practice. All participants receive the same arm training intervention.
Primary Outcome Measures
NameTimeMethod
Brain connectivity during functional MRIChange from baseline to end of treatment (3 weeks)

Brain activation during movement will be captured with functional MRI. Analyses will investigate changes in connectivity between brain regions.

Action Research Arm TestChange from baseline to end of treatment (3 weeks)

Behavioral assessment of arm function. Scores range from 0 to 57 with a higher score equating to better function.

Brain activation during functional MRIChange from baseline to end of treatment (3 weeks)

Brain activation during movement will be captured with functional MRI. Analyses will investigate changes in magnitude of activation.

Secondary Outcome Measures
NameTimeMethod
Box & Blocks TestChange from baseline to end of treatment (3 weeks)
Grip StrengthChange from baseline to end of treatment (3 weeks)
Confidence in Arm and Hand Movements QuestionnaireChange from baseline to end of treatment (3 weeks)
Upper Extremity Fugl-Meyer Motor AssessmentChange from baseline to end of treatment (3 weeks)
Stroke Impact Scale Hand DomainChange from baseline to end of treatment (3 weeks)
9-Hole Peg TestChange from baseline to end of treatment (3 weeks)

Trial Locations

Locations (1)

University of South Carolina

🇺🇸

Columbia, South Carolina, United States

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