- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04403464
Effect of a New Interactive Device on the Motor and Functional Abilities of Children With Bilateral Cerebral Palsy
The Effect of Using a New Interactive Device Based on Motor Skill Learning Principles on the Motor and Functional Abilities of Children With Bilateral Cerebral Palsy
Recent research has shown that interventions with assistive technologies lead to an improvement in the motor and functional abilities of children with cerebral palsy (CP). REAtouch® is a new interactive interface based on motor skill learning principles. Its efficiency during intensive motor skill learning interventions has never been tested in children with bilateral cerebral palsy.
Therefore, the study aims to investigate the efficiency of using a virtual reality tool to provide a motor skill learning intervention in a randomized trial.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Recent research has shown that interventions with assistive technologies could lead to an improvement in the motor and functional abilities of children with cerebral palsy (CP). However they usually miss the functional motor skill learning qualities to match the changes observed in high intensity motor skill learning based interventions.REAtouch® is a new interactive interface based on motor skill learning principles that could be implemented in intensive interventions.
Therefore, the study aims to investigate the effects of intensive interventions with or without the interface on the motor and functional abilities of children with bilateral CP.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Yannick Bleyenheuft, Professor
- Phone Number: +32 2 764 93 49
- Email: yannick.bleyenheuft@uclouvain.be
Study Contact Backup
- Name: Seyma Kilcioglu, PhD Student
- Email: seyma.kilcioglu@student.uclouvain.be
Study Locations
-
-
-
Brussels, Belgium, 1200
- Recruiting
- Institute of Neuroscience, UCLouvain
-
Contact:
- Seyma Kilcioglu, PhD Student
- Email: seyma.kilcioglu@student.uclouvain.be
-
Contact:
- Yannick Bleyenheuft, PT, PhD
- Email: yannick.bleyenheuft@uclouvain.be
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosed bilateral cerebral palsy,
- MACS levels from I to III,
- GMFCS levels from I to III,
- Ability to follow instructions and complete testing.
Exclusion Criteria:
- Orthopedic surgery, botulinum toxin injections or another unusual intervention less than 6 months before or within the study period.
- Unstable seizure
- Severe visual or cognitive impairments likely to interfere with intervention or testing session completion
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HABIT-ILE with REAtouch®
Hand and Arm Bimanual Intensive Therapy Including Lower Extremities with an interactive device
|
65h HABIT-ILE including 30h REAtouch®
|
|
Active Comparator: HABIT-ILE without REAtouch®
Hand and Arm Bimanual Intensive Therapy Including Lower Extremities
|
65h HABIT-ILE
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Gross Motor Function Measure (GMFM-66):
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The GMFM has been developed to measure the change in gross motor function over time in children with cerebral palsy.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in ABILHAND-Kids Questionnaire
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
This ABILHAND-Kids Questionnaire has been developed to assess a child's unimanual and bimanual upper limb activities.
It ranges from - 6 to +6 logits (higher score means better performance).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Executive Functions
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Cognitive functions of the children will be assessed by Stroop task and Flanker task.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in spatial parameters of the gait (Kinematics assessments)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the stride length (meters), step length (meters) and step width (meters).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the gait (Cycle time)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the cycle of gait time (seconds).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the gait (Stance time)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the stance time (percentage of the total gait cycle).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the gait (Swing time)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the swing time (percentage of the total gait cycle).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the gait (Stride)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the gait cadence (stride per minute).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the gait (Velocity)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the gait velocity (meter/second).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in spatial parameters of the upper extremity (Straightness)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the straightness (percentage of upper extremity trajectory during a reaching task).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in spatial parameters of the upper extremity (Smoothness)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the smoothness (variability of the movement during a reaching task)
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in Test of Arm Selective Control (TASC)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The TASC is an upper limb selective motor control evaluation tool including eight motions in each arm and up to three attempts are allowed for each motion.
After completion of the best attempt, points ranging from 0 (absent), 1 (impaired) to 2 (normal) are recorded for each joint depending on the movement properties and descriptors of the test.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Selective Control Assessment of the Lower Extremity (SCALE)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The SCALE was designed to evaluate lower limb selective motor control of children with cerebral palsy.
The SCALE includes testing of five reciprocal lower extremity movements.
SVMC is graded at each joint as 'Normal' (2 points), 'Impaired' (1 point), or 'Unable' (0 points).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in 6 Minutes Walking Test (6MWT)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The 6 Minutes Walking Test measures the distance that the patient walk as much as possible within a period of 6-minutes in a 30 meters long corridor.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Box and Blocks test (BBT)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The BBT is a test of gross manual dexterity.
Each hand is tested individually and the BBT is scored through the number of blocks carried over the partition from one part to another part of a box during the one-minute trial period.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Jebsen-Taylor Test
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The Jebsen-Taylor Test assesses uni-manual hand function, through 7 subtests simulating daily life activities.
The test assesses speed, not quality of performance and time to complete each activity is reported using a stopwatch.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Modified Cooper test
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The Modified Cooper test is a modified version of The Manual Form Perception Test, which evaluates stereognosis through 16 objects.
Both hands are tested separately and time to recognise the objects is reported using a stopwatch.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in ACTIVLIM-CP Questionnaire
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The ACTIVLIM-CP Questionnaire measures a patient's ability to perform daily activities requiring the use of the upper and/or the lower limbs through 42 items specific to patients with cerebral palsy.
It ranges from - 5 to +5 logits (higher score means better performance).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in ABILOCO-Kids Questionnaire
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The ABILOCO-Kids Questionnaire measures a patient's ability to perform daily activities requiring the use of the lower limbs through 10 items specific to patients with cerebral palsy.
It ranges from - 4 to +4 logits (higher score means better performance).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Pediatric Evaluation of Disability Inventory Computer Adaptive Test (PEDI-CAT)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The PEDI-CAT is the new version of the Pediatric Evaluation of Disability Inventory (PEDI).
The PEDI-CAT is comprised of 276 functional activities acquired throughout infancy, childhood and young adulthood.
Based on the nternational Classification of Functioning, Disability and Health for Children and Youth (ICF-CY) model, the PEDI-CAT contents provide information about the activities and participation component.
It ranges from 0 to 100% (higher score means better performance).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Canadian Occupational Performance Measure (COPM)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The COPM measures the patient's self-perception of occupational performance and satisfaction of it in daily activities over time.
It ranges from 1 to 10 (higher score means better performance).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in Both Hands Assessment (BoHA)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
The BoHA is a videotaped tool measuring how effectively children with bilateral CP use both hands in bimanual activities.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow- up
|
|
Changes in temporal parameters of the gait (Acceleration)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the gait acceleration (meters/second^2).
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
|
Changes in temporal parameters of the upper extremity (Kinematics assessments)
Time Frame: pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Through a 3D motion system, we measure the time from onset to end of the task (seconds).
the task consists in a reaching task.
|
pre-camp (1 week before), post-camp (1 week after), 3 months follow-up
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Yannick Bleyenheuft, Professor, Institute of Neuroscience, UCLouvain
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- B403201316810e
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Cerebral Palsy
-
Ankara City Hospital BilkentRecruitingCerebral Palsy (CP) | Cerebral Palsy, Spastic, Diplegic | Diplegic Cerebral Palsy With Spasticity | Transcranial Magnetic StimilationTurkey (Türkiye)
-
Lahore University of Biological and Applied SciencesRecruiting
-
Suleyman Demirel UniversityCompletedCerebral Palsy | Hemiplegic Cerebral Palsy | Spastic Diplegia Cerebral PalsyTurkey (Türkiye)
-
Holland Bloorview Kids Rehabilitation HospitalCanadian Institutes of Health Research (CIHR)RecruitingCerebral Palsy (CP) | Hemiplegic Cerebral PalsyCanada
-
Cairo UniversityCompletedCerebral Palsy (CP) | Unilateral Cerebral PalsyEgypt
-
University of California, San FranciscoNot yet recruitingCerebral Palsy | Cerebral Palsy (CP) | Infant | Cerebral Palsy InfantileUnited States
-
Lahore University of Biological and Applied SciencesNot yet recruitingSpastic Diplegia Cerebral PalsyPakistan
-
IRCCS Fondazione Stella MarisNot yet recruitingCerebral Palsy (CP) | EEG | Unilateral Cerebral Palsy | Action ObservationItaly
-
IRCCS Fondazione Stella MarisUniversity of Siena, ItalyRecruitingCerebral Palsy (CP) | Motor Imagery | CP (Cerebral Palsy) | Action ObservationItaly
-
Gazi UniversityCompletedCerebral Palsy | Cerebral Palsy, Spastic | Cerebral Palsy Spastic Diplegia | Cerebral Palsy Quadriplegic | Cerebral Palsy, MonoplegicTurkey
Clinical Trials on HABIT-ILE with REAtouch®
-
Université Catholique de LouvainCompletedCerebral PalsyBelgium
-
Université Catholique de LouvainNot yet recruiting
-
Universidad Europea de MadridNot yet recruiting
-
Shriners Hospitals for ChildrenTeachers College, Columbia UniversityCompletedCerebral PalsyUnited States
-
Université Catholique de LouvainCompletedCerebral PalsyBelgium
-
University Hospital of Mont-GodinneUniversité Catholique de LouvainUnknownBimanual Training in Children With Hemiplegia With Lower Limb and Postural Stimulation (HABIT & Leg)Congenital HemiplegiaBelgium
-
Université Catholique de LouvainRecruitingCerebral PalsyBelgium
-
Université Catholique de LouvainRecruitingAcquired Brain InjuryBelgium
-
Université Catholique de LouvainUniversity of Pisa; University Hospital, Angers; University of the Balearic Islands and other collaboratorsActive, not recruitingCerebral PalsyFrance, Belgium, Italy
-
Université Catholique de LouvainRecruiting