on-invasive assessment of wrist flexion deformity in Cerebral Palsy and stroke
- Conditions
- Stroke10007963Cerebral PalsySpastic paresis
- Registration Number
- NL-OMON30960
- Lead Sponsor
- eids Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 40
Cerebral Palsy patients
Inclusion criteria
• Young patients with motor disorders resulting from Cerebral Palsy, that have an abnormal wrist posture, i.e. showing a spontaneous flexion deformity of more than 30°
• Age between 12 and 18 years ;Stroke patients
Inclusion criteria
• Patients in the subacute to chronic stage after stroke who have developed a wrist flexion deformity, i.e. showing a wrist flexion angle of more than 30° at rest.;Control subjects
Inclusion criteria
• Age- (within one year deviation per patient), sex-matched.
• Predominantly healthy.
Exclusion criteria CP
• A history of confounding morbidity around the wrist, e.g. fractures.
• Restricted vision (< 0.5)
• Loss of sensibility of the hand, preventing the patient from delivering the required task performance.
• Cognitive impairments preventing the patient from understanding the instructions required for the task that has to be performed.
• Other severe co- morbidity preventing patients from delivering the required task performance.
• Previous surgery on the wrist/ lower arm;Exclusion criteria stroke
• The same as for the CP patient group;Exclusion criteria control subjects
• History of previous or current neurological disorders of central origin or peripheral origin, e.g. Parkinson, Multiple Sclerosis, Stroke, nerve lesions, CRPS, plexus brachalis lesions etc.
• A history of confounding morbidity around the wrist, e.g. fractures..
• Restricted vision preventing subject from delivering the required task performance.
• Loss of sensibility of wrist, preventing from delivering the required task performance.
• Cognitive impairments preventing the subject from understanding the instructions required for the task that has to be performed.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Location of the optimal length and passive stiffness curve of the flexor<br /><br>muscles and passive stiffness under high frequency perturbations; location of<br /><br>the optimal length and passive stiffness curve of the extensor muscles; active<br /><br>stiffness during constant activity for both muscle groups; inertia of hand,<br /><br>viscosity of wrist joint under high frequency perturbations. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Passive and active range of motion of the wrist joint, neutral position of the<br /><br>wrist, maximum voluntary contraction, Zancolli score, Ashworth score, Tardieu<br /><br>score, selected tendon reflex tests</p><br>