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Clinical Trial Summary

The investigators will conduct a single-blind, randomized controlled trial of 60 patients with subacute stroke. Patients will be randomly assigned into a control group and an intervention group. The intervention group will participate in immersion VR training for 3 weeks. The control group will receive for traditional rehabilitation training for 3 weeks. Then, the patients will be reevaluated to determine changes in upper extremity function, cognitive function, cortical and subcortical activation patterns, and performance of activities of daily living after the baseline assessment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Immersion Virtual Reality Training ,Stroke, Upper Extremity, Randomized Controlled Trial
  • Stroke

NCT number NCT03086889
Study type Interventional
Source Second Affiliated Hospital of Wenzhou Medical University
Contact
Status Terminated
Phase N/A
Start date April 20, 2017
Completion date January 1, 2023