This study is in progress, not accepting new patients

Determinants of the Effectiveness of Robot-assisted Hand Movement Training

a study on Ischemic Stroke Cerebrovascular Accident Stroke

Summary

Eligibility
for people ages 18-85 (full criteria)
Location
at Irvine, California
Dates
study started
completion around
Principal Investigator
by David Reinkensmeyer, Ph.D

Description

Summary

The investigators would like to investigate the effectiveness of somatosensory training for robot-assisted hand motor rehabilitation after stroke.

Details

From previous studies, the investigators learned that stroke survivors with impaired finger proprioception did not achieve as large a functional benefit from robotic finger training. For this study, the investigators would like to determine if and the extent of finger proprioception can be improved through targeted robotic proprioceptive training combined with robotic finger movement training. The investigators would also include imagining studies via Electroencephalogram (EEG) and other baseline predictors to provide insight to determine who responds best to proprioceptive training.

Keywords

Stroke, Ischemic, Cerebrovascular Accident (CVA), Rehabilitation, Stroke, Ischemic Stroke, New FINGER

Eligibility

You can join if…

Open to people ages 18-85

  • Age 18 to 85 years
  • Suffered from a single ischemic stroke (radiologically confirmed) at least 6-months prior to enrollment
  • An ability to score at least 3 blocks on the Box and Block Test

You CAN'T join if...

  • A substantial decrease in alertness, language reception or attention
  • Pregnant or lactating
  • Advanced liver, kidney, cardiac or pulmonary disease
  • Plan to alter any current participation in other rehabilitation therapy in the time period of the study
  • A terminal medical diagnosis consistent with survival < 1 year
  • Coexistent major neurological disease
  • Coexistent major psychiatric disease
  • A history of significant alcohol or drug abuse in the prior 3 years
  • Current enrollment in another study related to stroke or stroke recovery
  • Any other medical contraindication to participation in this study evaluated by our team physician.

Location

  • University of California Irvine
    Irvine California 92697 United States

Lead Scientist at UC Irvine

Details

Status
in progress, not accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
University of California, Irvine
ID
NCT04818073
Study Type
Interventional
Participants
Expecting 60 study participants
Last Updated