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

Primary Purpose

Cerebral Palsy

Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
HABIT-ILE
Usual Care
Sponsored by
Université Catholique de Louvain
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Palsy focused on measuring motor skill learning, functional changes, neuroplastic changes, biomechanical changes

Eligibility Criteria

12 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

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.)

Sites / Locations

  • Institute of Neuroscience, Université catholique de Louvain
  • Fondation ILDYS - Site de Ty Yann
  • IRCCS Fondazione Stella Maris

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HABIT-ILE

Usual Care

Arm Description

Early HABIT-ILE (Hand and arm bimanual intensive therapy including lower extremities) will be applied over 2 weeks.

A two weeks period of usual customary care

Outcomes

Primary Outcome Measures

Change on Gross Motor Function (GMFM-66)
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))
Developed 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 Outcome Measures

Melbourne 2 Assessment (MA2)
assess the unilateral performance of the upper extremities, quantifying the dexterity, fluency, accuracy and range of movement during several tasks of reaching and manipulation
Inhibitory control task
Measures 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.
Working memory task
Measures 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 assessment
Through different simple tasks, measures the visual field, the visuo-motor coordination, the orientation of attention in the space and the eye pursuit.
Semmes-Weinstein monofilaments
Evaluates 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 Threshold
The 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 questionnaire
This 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)
This 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)
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 (higher score means better performance).
Measure of Processes of Care (MPOC-20)
Assesses 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)
This 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)
This sequence allows to measure changes in gray matter (cortical thickness)
Changes on the Fractional Anisotropy (Diffusion tensor imaging (DTI))
This 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))
This 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.
Changes on resting state functional connectivity (RS)
Resting-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
Changes on spatial parameters of the gait (Kinematics assessments)
Through 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)
Through a 3D motion system, we measure cycle of gait time (seconds).
Changes on temporal parameters of the gait (Stance time)
Through a 3D motion system, we measure the stance time (percentage of total gait cycle).
Changes on temporal parameters of the gait (Swing time)
Through a 3D motion system, we measure the swing time (percentage of total gait cycle).
Changes on temporal parameters of the gait (Stride)
Through a 3D motion system, we measure the gait cadence (stride per minute).
Changes on temporal parameters of the gait (Velocity)
Through a 3D motion system, we measure the gait velocity (meter/second)
Changes on temporal parameters of the gait (Acceleration)
Through a 3D motion system, we measure the gait acceleration (meters/second^2)
Changes on spatial parameters of the upper extremity (Straightness)
Through 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)
Through 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)
Through 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 activity
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/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.

Full Information

First Posted
November 20, 2018
Last Updated
May 24, 2022
Sponsor
Université Catholique de Louvain
Collaborators
University Hospital, Brest, University of Pisa, University Hospital, Angers, University of Lausanne Hospitals, University of the Balearic Islands, Fondation Paralysie Cérébrale
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1. Study Identification

Unique Protocol Identification Number
NCT04020354
Brief Title
Changes Induced by Early HABIT-ILE in Pre-school Children With Uni- and Bilateral Cerebral Palsy
Acronym
EarlyHABIT-ILE
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 27, 2018 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
June 30, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Université Catholique de Louvain
Collaborators
University Hospital, Brest, University of Pisa, University Hospital, Angers, University of Lausanne Hospitals, University of the Balearic Islands, Fondation Paralysie Cérébrale

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
motor skill learning, functional changes, neuroplastic changes, biomechanical changes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HABIT-ILE
Arm Type
Experimental
Arm Description
Early HABIT-ILE (Hand and arm bimanual intensive therapy including lower extremities) will be applied over 2 weeks.
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
A two weeks period of usual customary care
Intervention Type
Behavioral
Intervention Name(s)
HABIT-ILE
Intervention Description
Early Hand and arm bimanual intensive therapy including lower extremities
Intervention Type
Behavioral
Intervention Name(s)
Usual Care
Intervention Description
Usual customary care
Primary Outcome Measure Information:
Title
Change on Gross Motor Function (GMFM-66)
Description
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)
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up.
Title
Change on Manual Ability (Assisting Hand Assessment (AHA))
Description
Developed 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)
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Secondary Outcome Measure Information:
Title
Melbourne 2 Assessment (MA2)
Description
assess the unilateral performance of the upper extremities, quantifying the dexterity, fluency, accuracy and range of movement during several tasks of reaching and manipulation
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Inhibitory control task
Description
Measures 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.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Working memory task
Description
Measures 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.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Visuo-spatial attention assessment
Description
Through different simple tasks, measures the visual field, the visuo-motor coordination, the orientation of attention in the space and the eye pursuit.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Semmes-Weinstein monofilaments
Description
Evaluates 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.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Pressure Threshold
Description
The 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.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Activlim-CP questionnaire
Description
This 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).
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Pediatric Evaluation of Disability Inventory questionnaire (PEDI)
Description
This 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).
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Young children's participation and environment measure (YC-PEM)
Description
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 (higher score means better performance).
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Measure of Processes of Care (MPOC-20)
Description
Assesses 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.
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
Canadian Occupational Performance Measure (COPM)
Description
This 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)
Time Frame
pre-camp, two weeks post-camp, 3 months follow-up
Title
3D T1-weighted structural imaging (T1)
Description
This sequence allows to measure changes in gray matter (cortical thickness)
Time Frame
pre-camp, 3 months follow-up
Title
Changes on the Fractional Anisotropy (Diffusion tensor imaging (DTI))
Description
This 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.
Time Frame
pre-camp, 3 months follow-up
Title
Changes on the Mean Diffusivity (Diffusion tensor imaging (DTI))
Description
This 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.
Time Frame
pre-camp, 3 months follow-up
Title
Changes on resting state functional connectivity (RS)
Description
Resting-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
Time Frame
pre-camp, 3 months follow-up
Title
Changes on spatial parameters of the gait (Kinematics assessments)
Description
Through a 3D motion system, we measure the stride length (meters), step length (meters) and step width (meters).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Cycle time)
Description
Through a 3D motion system, we measure cycle of gait time (seconds).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Stance time)
Description
Through a 3D motion system, we measure the stance time (percentage of total gait cycle).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Swing time)
Description
Through a 3D motion system, we measure the swing time (percentage of total gait cycle).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Stride)
Description
Through a 3D motion system, we measure the gait cadence (stride per minute).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Velocity)
Description
Through a 3D motion system, we measure the gait velocity (meter/second)
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the gait (Acceleration)
Description
Through a 3D motion system, we measure the gait acceleration (meters/second^2)
Time Frame
pre-camp, 3 months follow-up
Title
Changes on spatial parameters of the upper extremity (Straightness)
Description
Through a 3D motion system, we measure the straightness (percentage of upper extremity trajectory during a reaching task).
Time Frame
pre-camp, 3 months follow-up
Title
Changes on spatial parameters of the upper extremity (Smoothness)
Description
Through a 3D motion system, we measure the smoothness (variability of the movement during a reaching task)
Time Frame
pre-camp, 3 months follow-up
Title
Changes on temporal parameters of the upper extremity (Kinematics assessments)
Description
Through a 3D motion system, we measure the time from onset to end of the task (seconds). the task consist in a reaching task.
Time Frame
pre-camp, 3 months follow-up
Title
Quantification of physical activity
Description
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/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.
Time Frame
5 hours during 5 consecutive days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
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.)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yannick Bleyenheuft, Pr
Organizational Affiliation
MSL-IN Lab, Institute of Neuroscience, Université catholique de Louvain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Neuroscience, Université catholique de Louvain
City
Brussels
ZIP/Postal Code
1200
Country
Belgium
Facility Name
Fondation ILDYS - Site de Ty Yann
City
Brest
Country
France
Facility Name
IRCCS Fondazione Stella Maris
City
Marina Di Pisa-Tirrenia-Calambrone
State/Province
Toscana
ZIP/Postal Code
56128
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32290815
Citation
Araneda R, Sizonenko SV, Newman CJ, Dinomais M, Le Gal G, Nowak E, Guzzetta A, Riquelme I, Brochard S, Bleyenheuft Y; Early HABIT-ILE group. Functional, neuroplastic and biomechanical changes induced by early Hand-Arm Bimanual Intensive Therapy Including Lower Extremities (e-HABIT-ILE) in pre-school children with unilateral cerebral palsy: study protocol of a randomized control trial. BMC Neurol. 2020 Apr 14;20(1):133. doi: 10.1186/s12883-020-01705-4.
Results Reference
derived
Links:
URL
https://uclouvain.be/en/research-institutes/ions/cosy/motor-skill-learning-and-intensive-neurorehabilitation-lab-msl-in.html
Description
Lab website

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

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