To determine to what extent dynamic spasticity can be recognized and quantified in the gait pattern of children with spastic CP and to develop a meaningful and (clinically) applicable measure of dynamic spasticity
ID
Source
Brief title
Condition
- Congenital and peripartum neurological conditions
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary outcome measure is the difference in dynamic spasticity (*velocity
dependent muscle activation during gait*) between healthy children and children
with CP.
Secondary outcome
Not applicable
Background summary
Spasticity is defined as velocity dependent hypertonia (Lance, 1990), and is
apparent in 80% of children with Cerebral Palsy. In clinical practice,
spasticity is measured using passive muscle tests such as the (Modified)
Ashworth Scale or the (Modified) Tardieu Scale. However, it is difficult to
determine the precise effect of spasticity on gait. Crenna et al. (Crenna et
al., 1992; Crenna, 1998) introduced an interesting idea to look at spasticity
effects during gait, by looking at the relationship between muscle lengthening
velocity and muscle electromyographic (EMG) activity. They found that in
children with CP the coupling between muscle lengthening velocity and EMG
activity is often increased compared to normal. However, they did not translate
this idea into a workable algorithm, a measure that is (physiologically)
meaningful; that can be tested; and is clinically applicable. Therefore we will
set up a study to examine dynamic spasticity, i.e. the spasticity effects
during gait, in a group of children with spastic CP
Study objective
To determine to what extent dynamic spasticity can be recognized and quantified
in the gait pattern of children with spastic CP and to develop a meaningful and
(clinically) applicable measure of dynamic spasticity
Study design
(Pilot) study to compare groups: CP versus normal.
All subjects will be measured twice in the same way. They will get physical
examination to measure spasticity in a standard clinical way. Then instrumented
gait analysis will be performed. Subjects will walk on a 6m walkway at
comfortable walking speed, at a slow and a fast speed. 3D kinematics, kinetics
and electromyography will be measured.
Study burden and risks
The extensive data that will be collected are expected to give a better insight
and understanding of gait deviations than regular clinical examination will do.
In the (near) future, these additional data can lead to better diagnosis and
treatment.
The additional risks of the current study for the subjects are negligible and
the burdens minimal. The measurements are non-invasive. Subjects will have to
walk on a walkway with measurement tools (EMG electrodes and kinematic markers)
attached to their bodies. More markers and cables will be used than during
standard clinical practice, this may somewhat increase the burden of the
measurements compared to regular treatment. This is also the case because it
will take some more time to attach the markers, which will ask for patients of
the subjects. It should be noted that the current experimental set-up is
comparable to standard gait analysis as applied in many gait laboratories all
over the world for standard clinical practice.
We believe the benefits clearly outweigh the risks and burdens for the
subjects.
Postbus 7057
1007 MB Amsterdam
Nederland
Postbus 7057
1007 MB Amsterdam
Nederland
Listed location countries
Age
Inclusion criteria
Patients:
-Clinical diagnosis of Spastic Cerebral Palsy
-Diplegic or hemiplegic
-Age: between 6 and 12 years of age
-Male and female
-Independent walkers without walking aids (with or without AFO, GMFCS classification I or II (gross motor function classification system, (Wood and Rosenbaum, 2000)) ;Healthy controls
-Age-matched to CP
Exclusion criteria
Patients:
-Prior multilevel surgery, SDR or baclophen treatment.
-Prior BTX-A < 16 weeks
-Orthopaedic deformities that have major effect on gait
-The child*s movement pattern is mainly dyskinetic / ataxic
-Additional disorders (other than CP) that influence gait
-Parents or guardians and child do not understand the Dutch or English language well enough to take part in this project ;Healthy controls
-Any (known) deviation that may influence gait
-Parents or guardians and child do not understand the Dutch or English language well enough to take part in this project
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL11352.029.06 |