Quantifying spasticity using a robotic device: the QUASAR study
Not Applicable
- Conditions
- StrokeStroke - HaemorrhagicStroke - Ischaemic
- Registration Number
- ACTRN12619001123134
- Lead Sponsor
- Melbourne Health
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 35
Inclusion Criteria
Hemiparesis due to a unilateral single clinical stroke
Spasticity in the elbow flexors
Able to give informed consent
Exclusion Criteria
Co-morbid neurological conditions
Recent <6 months pharmacological treatment for spasticity including botulinum toxin and baclofen
Painful shoulder
Significant upper limb pathology e.g. osteoarthritis
Inability to follow a single-stage command
Presence of contractures in the affected upper limb
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method