Validity, reliability and reactivity of the sensory measurements in post stroke patients.
Not Applicable
- Conditions
- stroke
- Registration Number
- JPRN-UMIN000029009
- Lead Sponsor
- Keio university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Those with severe heart disease: unstable angina, accute myocardial infarction, decompensated congestive heart failure, acute pulmonary heart, arrhythmia with poor control, severe aortic valve stenosis, active Myocarditis, endocarditis etc. Persons with severe cognitive impairment, severe mental illness Persons judged inappropriate by a doctor for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method light touch and pressure sensation of paretic upper extrimity.
- Secondary Outcome Measures
Name Time Method motor function set of Stroke Impairment Assessment Set, SEP, Fugl-Mayer Assessment, ROM, modified Ashworth Scale.