Skip to main content
Clinical Trials/KCT0002696
KCT0002696
Recruiting
未知

Safety and effect on shoulder joint of a novel shoulder rehabilitation device

Wonkwang University Hospital0 sites36 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the nervous system
Sponsor
Wonkwang University Hospital
Enrollment
36
Status
Recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Subacute stroke patients who reported hemiplegic shoulder pain with a minimum visual analogue scale (VAS) of 3 points (0\-10 point scale) were recruited for 12 months consecutively from July, 2016\.

Exclusion Criteria

  • 1\) significant cognitive impairment (Korean version of Mini\-Mental State Examination, K\-MMSE \<15\) or language deficits that might affect the reliability of responses to outcome measure scales, 2\) pre\-existing shoulder pain prior to stroke, and 3\) definite shoulder dislocation of affected limb as seen on radiographs due to safety concern.

Outcomes

Primary Outcomes

Not specified

Similar Trials