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Efficacy Study of an Interactive Robot for the Rehabilitation of the Upper Limb in Children With Cerebral Palsy

Primary Purpose

Cerebral Palsy

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Robotic-assisted therapy
Classical therapy
Sponsored by
Cliniques universitaires Saint-Luc- 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 Robotic-assisted therapy, cerebral palsy, ICF

Eligibility Criteria

4 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cerebral palsy (hemi, quadri or di-plegia)
  • MACS > 1/5 (moderate to severe impairments)

Exclusion Criteria:

  • Botulinum toxin injection in the upper limb muscles
  • Intrathecal Baclofen for the upper limb spasticity
  • an unstable clinical condition contraindicating the upper limb rehabilitation treatments
  • cognitive disorders preventing the understanding of the instructions
  • other neurological or orthopedic pathology affecting the upper limb.

Sites / Locations

  • Institut royal de l'accueil du handicap moteur

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental: Robotic-assisted therapy

Classical therapy

Arm Description

All patients will receive a similar classical rehabilitation as a basis. the 10 patients of this group will receive a supplement of robotic-assisted therapy.

All patients will receive a similar classical rehabilitation as a basis. the 10 patients of this group will receive a supplement of classical rehabilitation.

Outcomes

Primary Outcome Measures

Kinematic

Secondary Outcome Measures

Manual Ability Classification System
Quality of Upper Extremity Skills Test
Box and Block test
strength
Abilhand-Kids scale
Pediatric Evaluation of Disability Inventory
MHAVIE

Full Information

First Posted
September 26, 2012
Last Updated
May 6, 2013
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
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1. Study Identification

Unique Protocol Identification Number
NCT01700153
Brief Title
Efficacy Study of an Interactive Robot for the Rehabilitation of the Upper Limb in Children With Cerebral Palsy
Official Title
Study of the Effectiveness of an Interactive Robot for the Rehabilitation of the Upper Limb in Children With Cerebral Palsy by Evaluating the 3 Fields of the ICF: A Prospective, Randomized, Controlled, Simple Blind Study.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Cerebral Palsy (CP) is a major cause of impairments in child population. This disease justifies an intensive and prolonged multidisciplinary rehabilitation which can be optimised by robotics. Our team has developed a robot designed to rehabilitate the child's upper limb. This robot allows the patient to perform active, passive, or assisted exercises. This therapy is designed to promote motor development in children with CP. Its finality is to improve patients' quality of life and participation. Several pilot studies evaluated the efficacy of robotic assisted therapy in children with CP but none RCT has been done. Then, the aim of the study is to evaluate the efficacy of robotic-assisted therapy in children with cerebral palsy by evaluating the 3 fields of the ICF (International Classification of Functioning, Disability and Health) and performing a prospective randomized controlled single blind trial. Therefore, all patients will benefit from a classical rehabilitation as a basis. Furthermore, patients of the control and experimental groups will receive a supplement of classical rehabilitation and robotic-assisted therapy, respectively.
Detailed Description
INTRODUCTION Cerebral Palsy (CP) is a major cause of impairments in child population. Indeed, CP affects two births per thousand (1). The brain damage is expressed by different neurological impairments and functional disabilities. These disabilities justify intensive and sustained multidisciplinary rehabilitation to reduce neurological impairments, to improve the activities and participation of patients, and, ultimately, their quality of life (2, 3, 4). Robotics interest has already been shown for lower limb rehabilitation (5). The development of the upper limb rehabilitation robotic devices started later. To better stimulate brain plasticity, these tools meet the actual recommendations existing in CP's rehabilitation (4). Indeed, the robots allow the execution of a large number of movements whose quality is controlled (6). A visual interface gives the patient a feedback of its movements (7), and offers exercises oriented functional tasks that have meaning for him (8) and the possibly dive into a virtual reality. All these elements justify the clinical development of robots to assist the therapists. In children with CP, several pilot studies have verified the clinical applicability of these tools (9-11). However, no randomized controlled study has been performed to evaluate the effectiveness of robotic-assisted therapy in children with CP (12). Moreover, no study evaluated the effect of these therapies on the three areas of the ICF : Many studies focus on impairments (e.g. muscle) without assessing the functional capacity of the patient: what about their ability in every day life? OBJECTIVES To perform a prospective, randomized, controlled, single blind trial to assess the efficacy of robotic-assisted therapy in children with cerebral palsy by evaluating the three fields of the ICF. METHODS Twenty patients enrolled at the "Institut Royal de l'Accueil du Handicap Moteur" (IRAHM) (1200 Brussels) will be included according to the following criteria: CP, whose location is unilateral (hemiplegia) or bilateral (diplegia, quadriplegia), with a MACS (Manual Ability Classification System) score > 1 (moderate to severe motor impairments) (13). The exclusion criteria are the following: injection in the upper member of botulinum toxin within 6 months or intrathecal baclofen used for the upper limb, an unstable clinical condition contraindicating the upper limb rehabilitation treatments, cognitive disorders preventing the understanding of the instructions or other neurological or orthopedic pathology affecting the upper limb. A randomisation of patients in two groups (control and experimental) will be performed, using a stratified randomization method to ensure the equivalence of the two groups for age, the location of the symptoms (diplegia, quadriplegia, left or right hemiplegia) and motor neurological impairments (MACS score). At IRAHM, each child benefits of 3 physiotherapy sessions and 2 occupational therapy sessions per week. Each session lasts 45 minutes. The children in the control group will see no change in their treatment. In the experimental group, 1 physiotherapy session and 1 occupational therapy session will be replaced by two sessions of intensive rehabilitation of the arm with the robot. In total for each group, each child will benefit from 40 sessions of 45 minutes over 8 weeks therapy Patients will be evaluated three times in the study: before the start of treatments, at the end of treatments, and 3 months after the end of treatments. Functional assessments will be carried out according to a protocol exploring the three fields of the ICF. Impairments will be evaluated by the score of Quality of Upper Extremity Skills Test (14), MACS (13), and the Box and Block test (15). Then, spasticity (with two scales), kinematics and strength of the paretic arm will be evaluated using the modified Ashworth and Tardieu scales, the ReaPLAN robot and a dynamometer, respectively (9, 16, 17). Disability will be evaluated via Abilhand-kids (18) and Pediatric Evaluation of Disability Inventory (19). Participation restrictions will be evaluated via the MHAVIE questionnaire (20). All assessments will be carried out by a occupational therapist, which will be not informed the group that the child is assigned (single-blind). All rehabilitation and assessment sessions will be conducted at the IRAHM. PERSPECTIVES From this study, we hope to demonstrate the efficacy of robotic-assisted therapy in children with cerebral palsy by evaluating the three fields of the ICF. These results could prove that this tool can be a significant complement for the CP rehabilitation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
Robotic-assisted therapy, cerebral palsy, ICF

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental: Robotic-assisted therapy
Arm Type
Experimental
Arm Description
All patients will receive a similar classical rehabilitation as a basis. the 10 patients of this group will receive a supplement of robotic-assisted therapy.
Arm Title
Classical therapy
Arm Type
Active Comparator
Arm Description
All patients will receive a similar classical rehabilitation as a basis. the 10 patients of this group will receive a supplement of classical rehabilitation.
Intervention Type
Other
Intervention Name(s)
Robotic-assisted therapy
Intervention Description
This robotic device is designed to intensively rehabilitate the upper limb. Indeed, this robot allows the patient to perform a lot of active, passive, or assisted exercises. The level of assistance is determined and provided by the robot in function of the patient capacity.
Intervention Type
Other
Intervention Name(s)
Classical therapy
Intervention Description
conventional therapy will be performed by therapists specialized in neuro-pediatric rehabilitation
Primary Outcome Measure Information:
Title
Kinematic
Time Frame
Change from Baseline in Kinematic at an expected average of 3 months and 6 months
Secondary Outcome Measure Information:
Title
Manual Ability Classification System
Time Frame
Change from Baseline in manual ability at an expected average of 3 months and 6 months
Title
Quality of Upper Extremity Skills Test
Time Frame
Change from Baseline in quality of upper extremity skills at an expected average of 3 months and 6 months
Title
Box and Block test
Time Frame
Change from Baseline in dexterity at an expected average of 3 months and 6 months
Title
strength
Time Frame
Change from Baseline in strength at an expected average of 3 months and 6 months
Title
Abilhand-Kids scale
Time Frame
Change from Baseline in activity of daily living at an expected average of 3 months and 6 months
Title
Pediatric Evaluation of Disability Inventory
Time Frame
Change from Baseline in activity of daily living at an expected average of 3 months and 6 months
Title
MHAVIE
Time Frame
Change from Baseline in parents' satisfaction of children activity daily living at an expected average of 3 months and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cerebral palsy (hemi, quadri or di-plegia) MACS > 1/5 (moderate to severe impairments) Exclusion Criteria: Botulinum toxin injection in the upper limb muscles Intrathecal Baclofen for the upper limb spasticity an unstable clinical condition contraindicating the upper limb rehabilitation treatments cognitive disorders preventing the understanding of the instructions other neurological or orthopedic pathology affecting the upper limb.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maxime Gilliaux, PhD student
Organizational Affiliation
Université Catholique de Louvain
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut royal de l'accueil du handicap moteur
City
Brussel
ZIP/Postal Code
1200
Country
Belgium

12. IPD Sharing Statement

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Efficacy Study of an Interactive Robot for the Rehabilitation of the Upper Limb in Children With Cerebral Palsy

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