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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04362800
Other study ID # MOOV (29BRC20.0046)
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 19, 2021
Est. completion date September 17, 2021

Study information

Verified date December 2021
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

One of the urgent priorities in the field of pediatric neuro-rehabilitation is the development of efficient early motor interventions for children with cerebral palsy (CP). Animal studies suggest that early intensive interventions are likely to have a significant impact on the organization of the brain and corticospinal tracts, reducing motor impairments and their medium and long-term consequences in children with cerebral palsy. Although most of the growth, development and cortical organization takes place in the time course of the first 2 years of life, most studies investigating the effectiveness of intensive rehabilitation and associated neurophysiological mechanisms have been conducted in school-aged children (> 6 years). In addition, the vast majority of these studies were conducted in children with unilateral CP, while the bilateral form of the pathology has the highest prevalence. It is therefore a priority to investigate the effectiveness of early interventions on the overall motor function of children with CP, especially in children with bilateral form of CP. Hand and Arm Bimanual Intensive Therapy Including Lower Extremities (HABIT-ILE) makes it possible to apply the concepts of structured motor learning and intensive treatment to both the upper limbs and the lower limbs and demonstrated improvements at both levels in school-aged children with unilateral CP and bilateral and then at all three International Classification of Functioning and Disability levels. The principles and content of HABIT-ILE can be applied to pre-school children and this method is promising for early neuro-rehabilitation.


Description:

The main objective of this study is to evaluate the effect of 10 days (i.e. 50 hours) of early HABIT-ILE (HABIT-ILE) on the overall motor function of children aged 1 to 4 with bilateral cerebral palsy in comparison to 10 days (50h) of spontaneous overall motor activity including usual rehabilitation (control group).


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date September 17, 2021
Est. primary completion date September 17, 2021
Accepts healthy volunteers No
Gender All
Age group 12 Months to 59 Months
Eligibility Inclusion Criteria: - Child with bilateral cerebral palsy proven to be spastic or dyskinetic - 1 to 4 years old inclusive (12 to 59 months) (age corrected if premature) able to follow instructions and to be able to carry out all the assessments, in accordance with his age - Being matched to a child according to age, etiology of CP / classification of motor function (GMFCS) - Signature of consent by the two holders of parental authority Exclusion Criteria: - Exceed 4 years and 11 months (59 months) during the internship evaluation period. - Uncontrolled epilepsy. - History of toxin injection or surgery in the 6 months preceding the study period or scheduled within 3 months (during the study period). - Visual or cognitive deficit preventing the child from seeing the games and interacting - Usual contraindications to magnetic resonance imaging (MRI) such as metal implants.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MRI
MRI at baseline and J90
Electro-Encephalography-High Density
Electro-Encephalography-High Density (children with unilateral PC only) at baseline and J90
3D and EMG analysis
3D and EMG analysis at baseline and J90
care and classic activities
physiotherapy and psychomotility. As needed weekly sessions of speech therapist or orthoptist and daily activities of the child.

Locations

Country Name City State
France Les Capucins Angers
France Fondation ILDYS - Site de Ty Yann Brest

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gross Motor Function Measure (GMFM) Measures change in gross motor function over time in children with cerebral palsy. The score range from 0 to 100 as a percentage. 100 is the best outcome. 1 hour
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