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Changes Induced by Early HABIT-ILE in Pre-school Children With Uni- and Bilateral Cerebral Palsy

Functional, Neuroplastic and Biomechanical Changes Induced by Early Hand and Arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) in Pre-school Children With Uni- and Bilateral Cerebral Palsy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04020354
Acronym
EarlyHABIT-ILE
Enrollment
100
Registered
2019-07-16
Start date
2018-11-27
Completion date
2022-06-30
Last updated
2022-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy

Keywords

motor skill learning, functional changes, neuroplastic changes, biomechanical changes

Brief summary

Studying in two randomized controlled trials (RCT) the changes induced by early HABIT-ILE in functional, neuroplastic and biomechanical assessment in children with unilateral and bilateral CP.

Detailed description

This study aims to evaluate the effect of two weeks of early Hand-arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) on bimanual performance in pre-school children with unilateral cerebral palsy (CP) and on gross motor function in those with bilateral CP, compared with two weeks of usual motor activity including usual rehabilitation (control group). We will assess further changes in unilateral performance tests, daily life activities questionnaires and executive function tests. Neuroplastic changes will be assessed using brain imaging (magnetic resonance imaging, MRI) and biomechanical changes will be assessed by using optoelectronic motion capture system with electromyography (EMG), to determine the effect of HABIT-ILE on movement pattern and quality.

Interventions

BEHAVIORALHABIT-ILE

Early Hand and arm bimanual intensive therapy including lower extremities

BEHAVIORALUsual Care

Usual customary care

Sponsors

University Hospital, Brest
CollaboratorOTHER
University of Pisa
CollaboratorOTHER
University Hospital, Angers
CollaboratorOTHER_GOV
University of Lausanne Hospitals
CollaboratorOTHER
University of the Balearic Islands
CollaboratorOTHER
Fondation Paralysie Cérébrale
CollaboratorOTHER
Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
12 Months to 59 Months
Healthy volunteers
No

Inclusion criteria

* children with unilateral or bilateral cerebral palsy (spastic or dyskinetic) * age 1 to 4 years 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 3months after the intervention time * severe visual impairments * severe cognitive impairments * contraindications to perform MRI assessments (Metal implants, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Change on Gross Motor Function (GMFM-66)pre-camp, two weeks post-camp, 3 months follow-up.Developed to assess the changes in gross motor function of children with cerebral palsy (scored in percentage), observed over time or after intervention for the second randomized controlled trial (RCT2)
Change on Manual Ability (Assisting Hand Assessment (AHA))pre-camp, two weeks post-camp, 3 months follow-upDeveloped to observe the efficacy of the assisting hand use, in children with unilateral cerebral palsy (scored in percentage), during bimanual activities for the first randomized controlled trial (RCT1)

Secondary

MeasureTime frameDescription
Working memory taskpre-camp, two weeks post-camp, 3 months follow-upMeasures the capacity to retain visual information in use, in a short period of time. It's assessed by hiding a toy in front of the child and asking him/her to find it from 4 possibilities.
Visuo-spatial attention assessmentpre-camp, two weeks post-camp, 3 months follow-upThrough different simple tasks, measures the visual field, the visuo-motor coordination, the orientation of attention in the space and the eye pursuit.
Semmes-Weinstein monofilamentspre-camp, two weeks post-camp, 3 months follow-upEvaluates the pressure threshold or the response to a touching sensation of the filament. It is quantified using a numerical grading ranging from high pression/clear touching sensation to a slight pression/slight touching sensation.
Pressure Thresholdpre-camp, two weeks post-camp, 3 months follow-upThe superior pressure threshold will be determined at the moment of any visible change in the child's reaction to the pression made by the algometer.
Activlim-CP questionnairepre-camp, two weeks post-camp, 3 months follow-upThis parent's filled questionnaire measures a patient's ability to perform daily activities requiring the use of the upper and/or the lower extremities through 43 items specific to patients with cerebral palsy. It ranges from - 7 to +7 logits (higher score means better performance).
Pediatric Evaluation of Disability Inventory questionnaire (PEDI)pre-camp, two weeks post-camp, 3 months follow-upThis parent's filled questionnaire measures the performance of the child in the daily life activities and movement domains, focusing on the capacity of upper extremities and lower extremities during this activities. It ranges from 0 to 100% (higher score means better performance).
Young children's participation and environment measure (YC-PEM)pre-camp, two weeks post-camp, 3 months follow-upBased 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 (higher score means better performance).
Measure of Processes of Care (MPOC-20)pre-camp, two weeks post-camp, 3 months follow-upAssesses the parents' perceptions of the care they and their children receive from children's rehabilitation treatment centres. Using a 8-point response scale, parents answer to 20 questions, indicating to what extent they have experienced the events or the situations described. A score of 7 means that they have experienced this aspect to a very great extent, or most of the time. A score of 1 means that they have not experienced this aspect at all. A score of 0 means that the question does not apply to them. There is no total score. However, because the statements are positively worded, higher total scores indicates that needs of the parents are being met to a great extent.
Canadian Occupational Performance Measure (COPM)pre-camp, two weeks post-camp, 3 months follow-upThis is an interview-setting designed to capture a patient's self-perception of performance and satisfaction of it in everyday activities, observed over time. During the 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; higher score means better performance/satisfaction)
3D T1-weighted structural imaging (T1)pre-camp, 3 months follow-upThis sequence allows to measure changes in gray matter (cortical thickness)
Changes on the Fractional Anisotropy (Diffusion tensor imaging (DTI))pre-camp, 3 months follow-upThis sequence allows to measure changes in the fractional anisotropy (FA) on the white matter tracts. FA is a scalar value (no unit) between zero and one that describes the degree of anisotropy of white matter water molecules.
Changes on the Mean Diffusivity (Diffusion tensor imaging (DTI))pre-camp, 3 months follow-upThis sequence allows to measure the mean changes in the diffusivity (MD). MD is a scalar value (no unit) between zero and one that describes the degree of molecular diffusion.
Melbourne 2 Assessment (MA2)pre-camp, two weeks post-camp, 3 months follow-upassess the unilateral performance of the upper extremities, quantifying the dexterity, fluency, accuracy and range of movement during several tasks of reaching and manipulation
Changes on spatial parameters of the gait (Kinematics assessments)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the stride length (meters), step length (meters) and step width (meters).
Changes on temporal parameters of the gait (Cycle time)pre-camp, 3 months follow-upThrough a 3D motion system, we measure cycle of gait time (seconds).
Changes on temporal parameters of the gait (Stance time)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the stance time (percentage of total gait cycle).
Changes on temporal parameters of the gait (Swing time)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the swing time (percentage of total gait cycle).
Changes on temporal parameters of the gait (Stride)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the gait cadence (stride per minute).
Changes on temporal parameters of the gait (Velocity)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the gait velocity (meter/second)
Changes on temporal parameters of the gait (Acceleration)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the gait acceleration (meters/second\^2)
Changes on spatial parameters of the upper extremity (Straightness)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the straightness (percentage of upper extremity trajectory during a reaching task).
Changes on spatial parameters of the upper extremity (Smoothness)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the smoothness (variability of the movement during a reaching task)
Changes on temporal parameters of the upper extremity (Kinematics assessments)pre-camp, 3 months follow-upThrough a 3D motion system, we measure the time from onset to end of the task (seconds). the task consist in a reaching task.
Quantification of physical activity5 hours during 5 consecutive daysWith 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/s\^2). These measurements will be performed during therapy in 5 consecutive days for the HABIT-ILE group and during a regular week for the Usual Care group.
Changes on resting state functional connectivity (RS)pre-camp, 3 months follow-upResting-state functional magnetic resonane imaging (rs-fMRI) evaluates the regional interactions that occur during the resting or task-negative state. The magnitud of the brain activation during rs-fMRI will be assessed
Inhibitory control taskpre-camp, two weeks post-camp, 3 months follow-upMeasures the inhibition of a motor answer. It's assessed by asking the child not to reach for a toy previously showed to play with. The maximum waiting time is 30 seconds.

Countries

Belgium, France, Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026