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Effect of functional power training on the walking ability of children with spastic cerebral palsy in the age of 4 to 10 years

Completed
Conditions
10042258
'Spastic Cerebral Palsy'
'spastic child'
Registration Number
NL-OMON40459
Lead Sponsor
Amsterdam Rehabilitation Research Center | Reade
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Children with diagnosis of predominantly spastic type of Cerebral Palsy, aged 4-10 years, being ambulant without assistive devices (GMFCS level I and II).
Parents and/or the children want to improve the walking ability of the child.
The children are able to follow instructions to perform the exercises and tests.

Exclusion Criteria

Treatment with botulinum toxin A in lower limb or serial casting of lower limb less than 6 months before the MegaPower training starts.
Treatment of selective dorsal rhizotomie less than 12 months before the MegaPower training starts.
Walking is not (yet) the preferred way to move around.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Primary study parameters;<br /><br>The objective primary outcome to measure the effect of the MegaPower training<br /><br>is the Muscle Power Sprint Test (MPST). The Goal Attainment Scaling (GAS) is<br /><br>the subjective, reported by the parents, primary outcome.<br /><br>The MPST is a 6 times 15 meter sprint test. Between the 6 sprints is a 10 sec<br /><br>break in which the child can turn and be ready for the next sprint. The time<br /><br>used for each sprint is measured with 0.01 second precision. Together with body<br /><br>height and weight power will be calculated and expressed in Watts. The MPST<br /><br>measures the anaerobic capacity of the child expressed in mean power and peak<br /><br>power. The reliability of the test is good (ICC=0.97).<br /><br>With GAS the extent of reaching the treatment goal will be measured. GAS is a<br /><br>sensitive, individual, evaluative measurement which describes the change of<br /><br>individuals or groups after treatment (ICC = 0.86).</p><br>
Secondary Outcome Measures
NameTimeMethod
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