- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05740605
Implementation of a HABIT-ILE Intervention at Home for Children With Bilateral Cerebral Palsy (HABITILEhome)
Implementation of a HABIT-ILE at Home Intervention for Children With Bilateral Cerebral Palsy: a Non-inferiority Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Cerebral Palsy (CP) is the most common cause of physical disability in children: it occurs in 1 to nearly 4 children in 1000 newborns worldwide. This major public health issue caused by abnormal brain development or damage during brain development result in different symptoms that vary from one patient to another. Even if all children with CP will develop motor symptoms (abnormal movement patterns and posture) some of them will also develop non-motor symptoms such as pain (75%), intellectual deficits (50%), language disorders (25%), epilepsy (25%), behavioral and sleep disorders (20-25%). The consequences of these symptoms are very variable and result in long-term functional deficits in the activities of daily living, such as dressing, eating, going to the bathroom, etc. To improve these patients' autonomy, intensive therapies based on motor skill learning (MSL) have been shown to be especially effective. Among these therapies, Hand-Arm Bimanual Intensive Therapy including Lower Extremities (HABIT-ILE) has been developed over the last decade in the MSL-IN laboratory of UCLouvain and has shown impressive improvements in children with CP. It is based on an intensive training of bimanual activities, with a systematic inclusion of lower limbs and trunk motor control. This therapy is given in the form of a rehabilitation camp of at least 50 hours on site. Therefore, the implementation of a classic HABIT-ILE, in day-camp requires a great commitment from the families who must travel to the camp location for two weeks of therapy. In addition, for patients living far from big cities or unable to travel, access to these therapies can be really complex. Moreover, these camps are applied in a group of 8-12 children. Each participant is accompanied by at least one therapist (physiotherapist or occupational therapist and sometimes student) trained in HABIT-ILE therapy. This implies that a HABIT-ILE camp requires minimum 12 trained therapists. Nonetheless, there is a lack of therapists that makes the implementation of these camps still challenging. In addition, the health requirements related to COVID-19 make it difficult to implement any kind of therapy and to assess patients' progress. Therefore, this health crisis has highlighted the importance of being able to offer home-based therapy. To answer the problematics of pandemic, accessibility and of lack of HABIT-ILE therapists, the idea of implementing HABIT-ILE at home was born. How could we implement MSL principles at home? Some of the key components of MSL are intensity, shaping of the task (with part- task and increasing difficulty), goal-oriented therapy, positive reinforcement and hands-off (voluntary movements by the patients, not guided by the therapist). To incorporate those principles and ensure the validity of the therapy, guidance by a trained HABIT-ILE supervisor is necessary. This supervision will be provided through remote telerehabilitation sessions. Virtual reality is well suited to implement MSL-IN principles and allows for remote communication with patients. Tele-reeducation devices are numerous: from classic commercials video game found in stores to devices made for rehabilitation. Alone these devices do not allow the implementation of all the principles of motor skill learning but with the supervision of therapists trained in HABIT-ILE supervision, this objective could be achieved. With the help of new technologies, will the HABIT-ILE supervisors be able to implement HABIT-ILE at home in a reliable and standardized way for children with CP aged 6 to 18 ? This RCT aims to assess if HABIT-ILE at home is not inferior to HABIT-ILE in camp regarding physical abilities, functional activities and participation of the participants.
Moreover, if the maintenance of skills during HABT-ILE camp at 3- and 6-months post-therapy has been proven, the question of improving them has not been investigated yet. Indeed, we know that in order to maintain the skills learned during the HABIT-ILE therapy, it is necessary to practice them on a daily basis. If a skill is not used it will lead to a cortical reorganization of the motor cortex at the expense of this skill. Thus, there is a persistent cycle of decreased utilization that leads to unfavorable cortical reorganization that leads to decreased utilization, etc. It is called "learned non-use". In order to reduce this phenomenon and thus improve the transfer of the HABIT-ILE skills into the daily life of the children, we wonder about the benefit of a post-therapy follow-up. Once again, the use of tele-rehabilitation can provide us a solution of daily delocalized therapy directly implemented at the patient's home and supervised remotely. Could the transfer of learned skills be improved with a follow-up at home post therapy? In order to answer this question, after the two weeks of both HABIT-IL modality, we will set up a HABIT-ILE telerehabilitation follow-up for 9 weeks. This study therefore also aims to assess if the patient's abilities could be potentialize with a follow-up than without a follow-up after two weeks of HABIT-ILE therapy.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Zélie Rosselli, Phd student
- Phone Number: +33 6 82 59 79 38
- Email: zelie.rosselli@uclouvain.be
Study Locations
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-
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Brussels, Belgium
- Recruiting
- MSL-IN Lab, Institue of Neurosciences, UCLouvain
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Contact:
- Zélie Rosselli, PT
- Phone Number: +32 2 764 54 46
- Email: contact-mslin@uclouvain.be
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Children with confirmed diagnosis of bilateral Cerebral Palsy
- Age 5 to 18 years old
- Ability to interact and understand simple instructions in order to complete assessments and therapy
- Availability of a caregiver for 6h30 per day during two weeks of therapy
Exclusion Criteria:
- Uncontrolled seizure
- Botulinum toxin injection in the last 6 months before the first assessment or during the therapy
- Intensive therapy in the last 6 months before the first assessment or during the therapy
- Surgery that could affect the assessments or therapy in the last 6 months before the first assessment or during the therapy
- Severe visual or cognitive impairments interfering with treatment and or assessments
- Any typical contraindication for MRI
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HABIT-ILE therapy at home without a HABIT-ILE follow-up at home
2 weeks of HABIT-ILE (Hand-Arm Bimanual Intensive Therapy Including Lower Extremities) therapy at home followed by 9 weeks of usual care
|
The HABIT-ILE therapy at home will follow the same principles as the classic HABIT-ILE.
The therapy will take place in the patient's home and a close person (caregiver) will accompany the patient during the therapy.
A device will be used to facilitate the implementation of home therapy.
Supervision of the therapeutic process will be done remotely by a team of trained supervisors.
One hour of remote supervision per day will be scheduled within 6.5 hours of therapy.
Other Names:
Usual care is all the weekly physiotherapy and occupational therapy sessions that the patient usually receives.
Other Names:
|
|
Experimental: HABIT-ILE therapy at home with a HABIT-ILE follow-up at home
2 weeks of HABIT-ILE (Hand-Arm Bimanual Intensive Therapy Including Lower Extremities) therapy at home followed by 9 weeks of HABIT-ILE follow-up at home
|
The HABIT-ILE therapy at home will follow the same principles as the classic HABIT-ILE.
The therapy will take place in the patient's home and a close person (caregiver) will accompany the patient during the therapy.
A device will be used to facilitate the implementation of home therapy.
Supervision of the therapeutic process will be done remotely by a team of trained supervisors.
One hour of remote supervision per day will be scheduled within 6.5 hours of therapy.
Other Names:
HABIT-ILE follow-up at home follow the same principles as classic HABIT-ILE but is delivered at the patient home with 4 hours per week in autonomy and 1 hour per week under supervision.
Other Names:
|
|
Active Comparator: Classic HABIT-ILE therapy without follow-up HABIT-ILE at home
2 weeks of classic HABIT-ILE (Hand-Arm Bimanual Intensive Therapy Including Lower Extremities) therapy on site followed by 9 weeks of usual care
|
Usual care is all the weekly physiotherapy and occupational therapy sessions that the patient usually receives.
Other Names:
HABIT-ILE ("Hand-Arm Bimanual Intensive Therapy including Lower Extremities") is an intensive therapy that continuously incorporates postural control and LE function.
This motor learning-based approach include specificity of the practice, motivation, shaping of the task, intensive blocks of training and Hands-Off.
Moreover, the therapy is goal-oriented to increase functional independence during daily living.
This therapy has shown impressive improvements in children with PC.
|
|
Active Comparator: Classic HABIT-ILE therapy with follow-up HABIT-ILE at home
2 weeks of classic HABIT-ILE (Hand-Arm Bimanual Intensive Therapy Including Lower Extremities) therapy on site followed by 9 weeks of HABIT-ILE follow-up at home
|
HABIT-ILE follow-up at home follow the same principles as classic HABIT-ILE but is delivered at the patient home with 4 hours per week in autonomy and 1 hour per week under supervision.
Other Names:
HABIT-ILE ("Hand-Arm Bimanual Intensive Therapy including Lower Extremities") is an intensive therapy that continuously incorporates postural control and LE function.
This motor learning-based approach include specificity of the practice, motivation, shaping of the task, intensive blocks of training and Hands-Off.
Moreover, the therapy is goal-oriented to increase functional independence during daily living.
This therapy has shown impressive improvements in children with PC.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change on Gross Motor Function (GMFM-66)
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
Developed to assess the changes in gross motor function of children with cerebral palsy (scored in percentage)
|
baseline, 2 weeks and 12 weeks after baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in the Both Hand Assessment (BOHA)
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The BoHA aims to measure the effective use of both hands in bimanual activity performance, as well as to quantify the possible side difference between hands.
(score in percentage)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in gross unimanual dexterity by the Box and block test (BBT)
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The BBT assess unimanual dexterity by quantifying the maximum of wooden blocks transferred from one space to the other during 1 minute (Higher scores indicate better performance)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in the Six Minutes' Walk Test (6MWT)
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The 6MWT assess endurance while walking 6 minutes without pause.
More distance walked (in meters) indicate better performance
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in activities of daily living assessed by ABILHAND-Kids questionnaires.
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
ABILHAND-Kids is a questionnaire that measures manual ability for children with upper limb impairments.
The scale measures a person's ability to manage daily activities that require the use of the upper limbs, whatever the strategies involved.
ABILHAND-Kids has been validated in cerebral palsy children (age 6-15).
21 manual activities perceived by the children parents.
Each item is answered on a 3-level scale (impossible, difficult, easy).
The item difficulty increases with bimanual involvement: higher score means better performance
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in activities of daily living assessed by PEDI questionnaire
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
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 these activities.
It ranges from 0 to 100% (higher score means better performance)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in activities of daily living assessed by ACTIVLIM-CP Questionnaire
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
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)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in activities of locomotion assessed by ABILOCO-Kids Questionnaire
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The ABILOCO-Kids questionnaire is a measure of locomotion ability for children with lower limb impairments.
The scale has been calibrated in children with cerebral palsy (age 6-15).
The Parent is asked to fill in the questionnaire by estimating their child's ease or difficulty in performing each activity.
During the evaluation, the 3-level response scale is presented to the parent.
The parent is asked to rate his/her perception on the response scale as 'Impossible', 'Difficult' or 'Easy'.
The activities not attempted by the child within the last 3 months are not scored and are entered as not applicable (check the question mark '?' on the scoring sheet).
The activities that the child does not perform because they are too difficult must be scored as 'Impossible'.
(higher score means better performance)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in the fine motor skills and functional activities of the hand assessed by the Jebsen Hand Fuction Test
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The Jebsen Hand Function Test (JHFT) assesses fine motor skills, weighted and non-weighted hand function activities during performance of activities of daily living. The JHFT consists of 6 items that measure: (a) fine motor skills; (b) weighted functional tasks; and (c) non-weighted functional tasks: Turning over a 3×5-inch card Picking up small common objects Simulated feeding Stacking checkers Picking up large light cans Picking up large heavy cans |
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in self-esteem assessed by the ESTIMILL-CP questionnaire
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The ESTIMILL-CP is self-completed by the children.
It consists of 26 illustrated items where the child must choose between "I identify with the situation" or "I don't identify with the situation" and then whether it's "a lot of similarity" or "not much".
The lower the score, the worse the self-esteem.
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in the PILS-CP questionnaire.
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
The PILS-CP questionnaire self-administrated (patients do not realize the life situation).
Patients are asked to estimate the involvement in performing each life situation.
During the evaluation, a 3-level response scale is presented to the patients.
Patients are asked to rate their participation on the response scale as either "I am not involved", "I am a little bit involved", "I am fully involved".
Life situations that the patients do not want to be involve are rated with "?"
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in lower limbs physical activity
Time Frame: During the 2 weeks of therapy
|
With a movement sensor on each wrist and on the leg, the percentage of total time spent in movement (Standing, walking or sitting) is measured.
Calculated in terms of the changes in the acceleration (m/s²).
|
During the 2 weeks of therapy
|
|
Changes in upper limbs physical activity
Time Frame: During the 2 weeks of therapy
|
With a movement sensor on each wrist and on the leg, the activities of both hand is quantified.
Calculated in terms of the changes in the acceleration (m/s²).
|
During the 2 weeks of therapy
|
|
Changes in the functional goals assessed by the Canadian Occupational Performance Measure (COPM) questionnaire.
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
In this interview, patients set up 5 activities considered difficult in daily life.
These are then assessed, in a 1 to 10 scale, regarding the patient'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)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes in 3D T1-weighted structural imaging.
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
This sequence allows to measure changes in gray matter (cortical thickness)
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes on the Fractional Anisotropy (Diffusion tensor imaging (DTI))
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
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.
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes on RS-fMRI
Time Frame: baseline, 2 weeks and 12 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
|
baseline, 2 weeks and 12 weeks after baseline
|
|
Changes on the Mean Diffusivity (Diffusion tensor imaging (DTI))
Time Frame: baseline, 2 weeks and 12 weeks after baseline
|
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.
|
baseline, 2 weeks and 12 weeks after baseline
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Novak I, Morgan C, Fahey M, Finch-Edmondson M, Galea C, Hines A, Langdon K, Namara MM, Paton MC, Popat H, Shore B, Khamis A, Stanton E, Finemore OP, Tricks A, Te Velde A, Dark L, Morton N, Badawi N. State of the Evidence Traffic Lights 2019: Systematic Review of Interventions for Preventing and Treating Children with Cerebral Palsy. Curr Neurol Neurosci Rep. 2020 Feb 21;20(2):3. doi: 10.1007/s11910-020-1022-z.
- Demers M, Fung K, Subramanian SK, Lemay M, Robert MT. Integration of Motor Learning Principles Into Virtual Reality Interventions for Individuals With Cerebral Palsy: Systematic Review. JMIR Serious Games. 2021 Apr 7;9(2):e23822. doi: 10.2196/23822.
- Sakzewski L, Bleyenheuft Y, Boyd RN, Novak I, Elliott C, Reedman S, Morgan C, Pannek K, Fripp J, Golland P, Rowell D, Chatfield M, Ware RS. Protocol for a multisite randomised trial of Hand-Arm Bimanual Intensive Training Including Lower Extremity training for children with bilateral cerebral palsy: HABIT-ILE Australia. BMJ Open. 2019 Sep 8;9(9):e032194. doi: 10.1136/bmjopen-2019-032194.
- Bleyenheuft Y, Gordon AM. Hand-arm bimanual intensive therapy including lower extremities (HABIT-ILE) for children with cerebral palsy. Phys Occup Ther Pediatr. 2014 Nov;34(4):390-403. doi: 10.3109/01942638.2014.932884. Epub 2014 Oct 1.
- Bleyenheuft Y, Dricot L, Gilis N, Kuo HC, Grandin C, Bleyenheuft C, Gordon AM, Friel KM. Capturing neuroplastic changes after bimanual intensive rehabilitation in children with unilateral spastic cerebral palsy: A combined DTI, TMS and fMRI pilot study. Res Dev Disabil. 2015 Aug-Sep;43-44:136-49. doi: 10.1016/j.ridd.2015.06.014. Epub 2015 Jul 13.
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 (Estimate)
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
- B4032022000142a
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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