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Clinical Trials/KCT0009693
KCT0009693
Completed
未知

The effect of action observation training combined with upper extremity robot therapy on upper extremity function, activity daily living, electromyography in subacute stroke patients

Cheongju University0 sites24 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Cheongju University
Enrollment
24
Status
Completed
Last Updated
last year

Overview

Brief Summary

Both groups demonstrated significant improvements in upper extremity function, qualitative movement level, activities of daily living, and muscle activity post-intervention compared to pre-intervention. In the between-group comparison of changes after the intervention, the investigational group exhibited significantly greater improvements in upper extremity function, activities of daily living, and muscle activity than the control group. Coordination correlation ratios (CCR) showed negative values for all measured movements in the investigational group, whereas in the control group, only shoulder flexion movement showed a negative value.

Registry
who.int
Start Date
TBD
End Date
October 12, 2023
Last Updated
last year
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Cheongju University

Eligibility Criteria

Inclusion Criteria

  • Participant inclusion criteria
  • \- Patients with subacute stroke with stroke onset between 2 and 6 months ago
  • \- Patients with a Korean Version of Montreal Cognitive (K\-MoCA) score \=23
  • \- Patients judged to have no visual abnormalities using the Motor\-Free Visual Perception Test\-3 (MVPT\-3\)
  • \- Patients judged not to have unilateral neglect based on the Line Bisection Test (LBT)
  • \- Patients showing Brunnstrom Recovery Stage (BRS) \=3 in the upper limb on the affected side

Exclusion Criteria

  • Participant exclusion criteria
  • \- Patients diagnosed with a neurological deficit or surgical disease other than stroke, based on medical records
  • \- Patients judged to have lost proprioception based on findings by the attending physician
  • \- Patients judged to have difficulty participating in the study because of a pain score \=4 in the affected upper limb based on the Numeric Rating Scale (NRS)
  • \- Patients already participating in other research

Outcomes

Primary Outcomes

Not specified

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