Cerebral Palsy
Conditions
Brief summary
Using a randomized controlled trial design, the possible changes induced by the intensive treatment programme Hand-arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) in functional, everyday life activities and neuroplastic assessment will be studied in infants and toddlers with cerebral palsy.
Detailed description
Using a randomized controlled trial design, the possible changes in neuroimaging, motor function and everyday life activities of infants and toddlers at risk of or with a diagnosis of cerebral palsy after participating of the intensive treatment programme Hand-arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) will be studied . Changes, scored by parents in case of questionnaires and by experts in the case of tests, will be observed comparing infants/toddlers after their regular care and after receiving HABIT-ILE. Motor function and daily life activities will be correlated with neuroplastic changes. Moreover, possible therapy onset outcomes differences will be observed.
Interventions
motor learning-based, intensive therapy for children with cerebral palsy
BEHAVIORALRegular care
customary or usual care given to any infant/toddler with cerebral palsy
Sponsors
University Hospital of Mont-Godinne
Université Catholique de Louvain
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)
Intervention model description
Allocation
Eligibility
Sex/Gender
ALL
Age
8 Months to 18 Months
Healthy volunteers
No
Inclusion criteria
* children with diagnosed unilateral cerebral palsy or at risk of developing unilateral cerebral palsy or with signs of unilateral cerebral palsy * age 8 to 18 months inclusive (corrected age if preterm birth) * ability to follow instructions and complete testing according to the age.
Exclusion criteria
* active seizure * programmed botulinum toxin or orthopedic surgery in the 6 months previous to the intervention, during intervention period or 6 months after the intervention time. * severe visual impairments * severe cognitive impairments * contraindications to perform magnetic image resonance (MRI) assessments (metal implants, etc.)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes on the Mini-Assisting Hand Assessment (Mini-AHA) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Measures how well infants (8-18 months) with signs of unilateral or hemiplegic cerebral palsy use their more affected hand, when using both hands together to play (scored in percentage). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in Bayley Scales of Infant and Toddler Development - Third Edition (BSID-III) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Assess the development of infants and toddlers (1-42 months); three subitems will be considered, the Cognitive Scale, including assessments of attention (familiar and unfamiliar objects, looking for a fallen object, and pretend play), the Language Scale, including understanding and expression of language (recognition of objects and people, following directions, and naming objects and pictures), and the Motor Scale, assessing gross and fine motor skills (including grasping, sitting, stacking blocks, and climbing stairs). Raw scores of the items are converted to scale scores and composite scores (Mean 100, SD 15) ranging from 40 to 160 (higher scores indicates better performance). |
| Changes in Gross Motor Function Measure - 66 (GMFM-66) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Assess gross motor function of children with cerebral palsy (scored in percentage) |
| Changes in Visuo-spatial attention assessment with the Batterie d'évaluation du Jeune Enfant (BAJE) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Through different simple tasks, measures the visual field, the visuo-motor coordination, the orientation of attention in the space and the eye pursuit. |
| State of visual impairment of peripheral origin assessed with the standard Battery of Ophthalmological test for infants | baseline | Clinical assessment will be performed to describe the baseline of the ophthalmological condition. The ophthalmologist search for any abnormal signs of the eyes denoting the presence (or not) of visual impairments. |
| Changes in Pediatric Evaluation of Disability Inventory-Computer Adaptive Test (PEDI-CAT) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Parent's filled questionnaire measuring the performance of the child in the daily activities and mobility domains, focusing on the capacity of upper and lower extremities during these activities, computed through the PEDI-CAT software (scores reported in scaled scores). |
| Changes in Young children's participation and environment measure (YC-PEM) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Based in different children's activities, this parent's filled questionnaire evaluates the level of participation and the quality of the environment in which these activities take place. For each type of activity, caregivers assess 3 dimensions of the child's participation: frequency (8-point scale; 0-7), level of involvement (5-point scale; 1-5), caregiver's percent desire for change (2-points level (y/n) transformed in percentage; 0-100) and perceived impact of environmental support (3-point scale transformed in percentage; 0-100). A software calculates the total score with a maximum of 212 |
| Changes in Canadian Occupational Performance Measure (COPM) | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | In this interview, parents set up 5 activities considered difficult in daily life. These are then assessed, in a 1 to 10 scale, regarding the child's self-perception of performance and satisfaction of it. The total score is the average of the scores for perception and satisfaction separately (score from 1 to 10) |
| Changes in smoothness on kinematics of the upper extremity | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Through a 3D motion system, we measure the variability of the movement during a reaching task. |
| Changes in straightness on kinematics of the upper extremity | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Through a 3D motion system, we measure the percentage of upper extremity trajectory during a reaching task. |
| Changes in the quantification of physical activity | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | With a movement sensor on each wrist, the percentage of total time spent in movement (i.e. crawling, walking and running) is measured. Calculated in terms of the changes in the acceleration (m/s2). |
| Changes in cortical thickness of the brain's gray matter | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Regional brain cortical thickness is acquired from high resolution 3D T1-weighted structural imaging data. For each investigated region, mean cortical metrics (in millimeters) are assessed between the pial surface and the white/grey boundary. |
| Changes in Fractional Anisotropy (FA) of the corticospinal tract from the motor cortex to the cerebellar peduncle | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | FA is a scalar value (no unit) between 0 and 1 that describes the degree of anisotropy of white matter water molecules. It is measured non-invasively via brain MRI using diffusion tensor imaging (DTI), a modality of Diffusion-Weighted Imaging (DWI). Increased values indicate a higher directionality of the tissue structure. |
| Changes on the Axial, Radial and Mean Diffusivity (AD, RD, MD) of the corticospinal tract from the motor cortex to the cerebellar peduncle | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | AD, RD and MD are values ranging from 0 to 3.10-3 \[mm2/s\] that describe the degree of axial, radial and mean molecular diffusion of white matter water molecules. It is measured non-invasively via brain MRI using diffusion tensor imaging (DTI), a modality of Diffusion-Weighted Imaging (DWI). An increased MD can be considered to be an indicator of white matter damage. |
| Changes on the metrics of the corticospinal tract from the motor cortex to the cerebellar peduncle using the NODDI model | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | The orientation dispersion index (ODI), intracellular volume fraction (ICVF) and the fraction of the isotropic compartment (ISOF) are scalar values ranging from 0 to 1 (no units) that describe the orientation of neural fibers, and the volume fraction of the intracellular and isotropic compartment. It is measured non-invasively via brain MRI using the Neurite Orientation Dispersion and Density Imaging (NODDI) model combined with a Diffusion-Weighted Imaging (DWI) sequence. The results reflects the overall coherence of the fibers, with zero representing highly coherent structures, hence less dispersion of the fibers. |
| Changes of the fraction and heterogeneity in the neural fibers or isotropic compartments of the corticospinal tract from the motor cortex to the cerebellar peduncle using the DIAMOND model | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | By representing each voxel of the brain as the sum of multiple compartments (representing either a neural fiber population or an isotropic diffusion), the volume fraction (frac, ranging from 0 to 1, no unit) and heterogeneity (HEI, ranging from 0 to 1, no unit) of each compartment can be estimated. These metrics are measured non-invasively via brain MRI using the DIstribution of 3D Anisotropic MicrOstructural eNvironments in Diffusion-compartment imaging (DIAMOND) model combined with a Diffusion-Weighted Imaging (DWI) sequence. |
| Changes in resting-state functional connectivity | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Resting-state functional magnetic resonance imaging (rs-fMRI) evaluates the regional interactions that occur during the resting or task-negative state. The magnitude of the brain activation during rs-fMRI will be assessed |
| Changes in brain white matter microstructure (WM-μs) using the Microstructure Fingerprinting model | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Using a multiple-compartment approach, the signal obtained from a voxel can be estimated as the sum of multiple fiber populations, each presenting a specific fraction ('frac', ranging from 0 to 1, no unit), fiber volume fraction ('fvf', ranging from 0 to 1, no unit) and diffusivity ('diff', in \[mm2/s\]). On top of those fiber populations, isotropic compartments can also be represented with a specific fraction (frac) and diffusivity (diff). These metrics are measured non-invasively via brain MRI using the Microstructure Fingerprinting model combined with a Diffusion-Weighted Imaging (DWI) sequence. |
| Changes in time of activity on kinematics of the upper extremity | baseline, 3 weeks, 13 weeks and 26 weeks after baseline | Through a 3D motion system, we measure the time from onset to end of the task (in seconds) during a reaching task. |
Countries
Belgium
Contacts
Primary ContactYannick Bleyenheuft, PhD
Backup ContactDaniela Ebner, PhD
Outcome results
None listed