Safety and effect on shoulder joint of a novel shoulder rehabilitation device
Not Applicable
Recruiting
- Conditions
- Diseases of the nervous system
- Registration Number
- KCT0002696
- Lead Sponsor
- Wonkwang University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 36
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.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method visual analogue scale
- Secondary Outcome Measures
Name Time Method Passive range of motion of shoulder, PROM;Korean version of Shoulder disability questionnaire, K-SDQ;Ultrasonographic grading