Cerebral Palsy Clinical Trial
Official title:
A Randomized Cross-over Design Evaluating the Effects of Using a Rehabilitation-specific Gaming Software Platform for the Achievement of Individual Physiotherapy Goals of Children With Severe Spastic Cerebral Palsy.
The aim of this project is to evaluate the effectiveness of using rehabilitation-specific
gaming in physical therapy of children with cerebral palsy.
The primary goal of this project is to evaluate the effectiveness of integrating 15 to 20
minutes of gaming using a rehabilitation-specific gaming platform into standard physiotherapy
sessions on the achievement of individual goals of children with bilateral spastic cerebral
palsy with GMFCS level III-IV.
The secondary goal of this project is to evaluate the effectiveness of integrating 15 to 20
minutes of gaming using a rehabilitation-specific gaming platform into standard physiotherapy
sessions on trunk control and gross motor function of children with bilateral spastic
cerebral palsy with GMFCS level III-IV.
Forty children are recruited via the Cerebral Palsy Reference Centre (University Hospital
Leuven, Pellenberg). Children are recruited when they have been diagnosed with bilateral
spastic CP, Gross Motor Function Classification (GMFCS) level III-IV, aged between 6 and 15y
and standardly receive physiotherapy at an intensity of minimally 2 times per week, 45
minutes per session.
Children are randomized into the intervention group (conventional, usual therapy including
the use of rehabilitation-specific gaming) or the control group (PT, usual physiotherapy not
including gaming), followed by a cross-over. After the intervention period of 3 months,
wash-out period will be organized to evaluate follow-up effects.
During the intervention period, the usual individual physiotherapy program of the child will
be continued as performed before the study and will be executed by the child's usual,
familiar physiotherapist. The therapist will be asked to use the rehabilitation-specific
gaming software every therapy session, for at least 15 to 20 minutes. The therapist will
receive an extensive introduction and demonstration of the software and the researchers will
participate in at least one therapy session.
During the control period, the usual, conventional physiotherapy of the child will be
continued and the therapist will be asked not to use any gaming activities. Also during the
control period, the frequency and duration of the therapy sessions will not be influenced by
the researchers.
A wash-out period in between both programs, assumes that therapy effects are still present
for a certain period after the intervention and therefore aims to wash-out these effects.
Therefore, this period is considered after each intervention period. As during the control
period, therapy will be continued as usual during the washout-period but no gaming is allowed
during therapy.
All intervention and control periods will have the same duration of 3 months. During all
periods, therapists will receive a diary to register the exact amount of therapy performed.
The diary that will be provided during the intervention, will also question the specific
games played and will register the therapy goals strived for.
Children will be evaluated before and after each intervention or control period using a
multidimensional assessment protocol. In addition, children will also receive a follow-up
evaluation 3 months after the last intervention period. This will result in 4 evaluation
moments for each child. The evaluation exist of the Goal Attainment Scale, the Gross Motor
Function Measure, the Pediatric Balance Scale, the Trunk Control Measurement Scale and the
Dimensions of Mastery Motivation Questionnaire (DMQ).
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