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Clinical Trial Summary

The investigators have developed the kinect-based upper extremity rehabilitation program and designed this protocol to prove the efficacy of this program.

In brief, subacute stroke patients allocated to intervention group will receive the kinect based-rehabilitation program plus conventional occupational therapy and patients allocated to control group will receive the sham virtual rehabilitation plus conventional occupational therapy, for 10 days.

20 patients with subacute stroke will be allocated into each group and after completing the 10 days intervention, they will be assessed by using objective assessment tools for upper extremity function.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02066116
Study type Interventional
Source Seoul National University Bundang Hospital
Contact
Status Terminated
Phase N/A
Start date November 2014
Completion date November 2017

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