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Deficit Fields for Stroke Recovery

Not Applicable
Completed
Conditions
Stroke
Interventions
Behavioral: Deficit-fields to reduce error
Behavioral: Deficit-fields to improve function
Behavioral: Deficit-fields to expand range of motion
Registration Number
NCT02570256
Lead Sponsor
Shirley Ryan AbilityLab
Brief Summary

This study investigates the potential of customized robotic and visual feedback interaction to improve recovery of movements in stroke survivors. While therapists widely recognize that customization is critical to recovery, little is understood about how take advantage of statistical analysis tools to aid in the process of designing individualized training. Our approach first creates a model of a person's own unique movement deficits, and then creates a practice environment to correct these problems. Experiments will determine how the deficit-field approach can improve (1) reaching accuracy, (2) range of motion, and (3) activities of daily living. The findings will not only shed light on how to improve therapy for stroke survivors, it will test hypotheses about fundamental processes of practice and learning. This study will help us move closer to our long-term goal of clinically effective treatments using interactive devices.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
45
Inclusion Criteria

STROKE SURVIVORS:

  • adult (age >18)
  • Chronic stage stroke recovery (8+ months post)
  • available medical records and radiographic information about lesion locations
  • strokes caused by an ischemic infarct in the middle cerebral artery
  • primary motor cortex involvement
  • a Fugl-Meyer score (between 15-50) to evaluate arm motor impairment level

HEALTHY CONTROL PARTICIPANTS:

  • adult (age >18)
  • healthy individuals with no history of stroke or neural injury
Exclusion Criteria
  • bilateral paresis;
  • severe sensory deficits in the limb
  • severe spasticity (Modified Ashworth of 4) preventing movement
  • aphasia, cognitive impairment or affective dysfunction that would influence the ability to perform the experiment
  • inability to provide an informed consent
  • severe current medical problems
  • diffuse/multiple lesion sites or multiple stroke events
  • hemispatial neglect or visual field cut that would prevent subjects from seeing the targets.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Deficit-fields to reduce errorDeficit-fields to reduce errorWe hypothesize that a deficit-field design, using the statistics of a patient's errors to customize training, will provide optimal augmentation that varies during motion as needed. We will compare the training effects of error deficit-fields with previous methods of error augmentation to improve reaching ability.
Deficit-fields to improve functionDeficit-fields to improve functionHere we present visual distortion of whole body movement during manual tasks during standing, including reaching, grasping, and object manipulation. We compare the training effects of feedback based on deficit-fields versus practice with normal vision.
Deficit-fields to expand range of motionDeficit-fields to expand range of motionAmplifying augmentation can expand motor exploration and improve skill retention in patients. Using motor exploration patterns from each patient, we will form customized deficit-fields to recover normal joint workspace. We will compare augmentation training that either amplifies or diminishes the observed deficits (Expt-1). We also compare deficit-fields with our prior augmentation methods to determine the added value of increased customization (Expt-2).
Primary Outcome Measures
NameTimeMethod
Arm motor recovery scores on the Fugl-MeyerBaseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change from baseline in arm motor recovery as measured by Fugl-Meyer

Secondary Outcome Measures
NameTimeMethod
Modified Ashworth Scale (MAS)Baseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change from baseline in amount of spasticity in elbow flexors and extensors

Time and completion score for Action Research Arm Test (ARAT)Baseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change in baseline score and time for completion of functional measures as part of ARAT

Number of blocks transferred in Box and Blocks TestBaseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change from baseline in number of blocks transferred during Box and Blocks Test

Elbow active range of motion (ROM)Baseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change from baseline measured in degrees for elbow flexion and extension

Chedoke McMaster Stroke Assessment for HandBaseline at beginning of week 1 and 3 prior to intervention; post-evaluation at end of week 4; follow-up evaluation at end of week 5

Change in baseline in amount of hand motor recovery as measured by Chedoke scale

Trial Locations

Locations (1)

Rehabilitation Institute of Chicago

🇺🇸

Chicago, Illinois, United States

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