The Effectiveness of Robotic Assisted Gait Training as an Adjunct to Traditional Physiotherapy in Cerebral Palsy (RAGT)
Primary Purpose
Cerebral Palsy
Status
Completed
Phase
Not Applicable
Locations
United Arab Emirates
Study Type
Interventional
Intervention
Lokomat training
Sponsored by
About this trial
This is an interventional treatment trial for Cerebral Palsy focused on measuring Children, Lokomat
Eligibility Criteria
Inclusion Criteria:
Cerebral palsy with spastic and mix form
- Gross Motor Function Classification System (GMFCS from level II to IV)
- Age 4 to 18
- No contraindications for the training in the Lokomat
- Able to follow simple instructions
Exclusion Criteria:
On botox injection within the last 6 months (as the effect of botox wear out in 6 months)
- Surgery within the last one year
- Fixed contractures and/or with bone instability
- Baclofen infusion pumps in situ
- Seizure disorder that is not controlled by medication (if on medication, must not have had a seizure in the last 12 months);
- Open skin lesions or vascular disorder of lower extremities;
- Having participated in another Lokomat training regime within the previous 3months as well as a change in concomitant treatment within the last 4 weeks before or during the study period
Sites / Locations
- Fatima College of Health Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Robotic -assisted gait training group using Lokomat device
Traditional therapy group
Arm Description
5 sessions of 40 minutes of conventional therapy and 5 sessions of 40 minutes on Lokomat per week
• 5 sessions of 40 minutes of conventional therapy
Outcomes
Primary Outcome Measures
Gross Motor Function Measure ( GMFM- 88) - dimension D & dimension E
This is the validated test designed to measure change in gross motor function over time in children with cerebral palsy. Dimension D consist of 13 items for standing ability and dimension E has 24 items to assess walking, jumping and running in cerebral palsy children. Its a four point scoring system. Specific descriptors for each score is given in the Manual of GMFM-88.
6 minute Walk test
The test has been selected as a measure of gait endurance. This is validated test requiring individuals to walk 6 minutes on flat hard floor. Scoring is walking distance.
10 meters Walk test
The test has been selected as a measure of gait speed. This is validated test requiring individuals to walk on flat hard floor at their comfortable speed for 10 meters.
Pediatric Balance Scale
14 items valid scale is used to assess functional balance skills in children with spastic cerebral palsy.
Cerebral Palsy Quality of Life questionnaire for child (CP QOL-child) and Cerebral Palsy Quality of Life questionnaire for adolescent (CP QOL- teen)
This Arabic validated CP QOL- child for age 4-12 and CP QOL- teen for age 13-18 questionnaires are used in the parent version. Its assesses 7 domains on a 9 level point Likert scale.
Secondary Outcome Measures
Range of motion
Measuring range of motion in hip, knee, ankle joint using the reliable tool called goniometer.
The Oxford scale
The most commonly used scale for testing muscle strength.
Modified Ashworth Scale
It is a muscle tone assessment.
Full Information
NCT ID
NCT04960683
First Posted
January 13, 2021
Last Updated
March 24, 2022
Sponsor
Fatima College of Health Sciences
1. Study Identification
Unique Protocol Identification Number
NCT04960683
Brief Title
The Effectiveness of Robotic Assisted Gait Training as an Adjunct to Traditional Physiotherapy in Cerebral Palsy
Acronym
RAGT
Official Title
The Effectiveness of Robotic Assisted Gait Training as an Adjunct to Traditional Physiotherapy in Cerebral Palsy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
November 8, 2020 (Actual)
Primary Completion Date
July 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fatima College of Health Sciences
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
Need for study
There are a few studies published on this topic from various parts of the globe and the results are mixed. Hence further research is required in this area and none of the studies have included samples from the Middle East.
Some studies done in this area focus on biomechanical aspects of gait (Cherni, 2018) and our study mainly focuses on functional aspects of gait and quality of life.
Studies done on this area focus highly on gait components and very little is available on the literature on improving balance. Since balance and stability are crucial for walking, it was decided to exclusively assess balance.
Due to a wide range of therapeutic benefits, it is paramount to evaluate the effectiveness of different therapies provided to improve gait.
Aim of the study:
The aim of the proposed research is to investigate the effectiveness of robotic assisted gait training using Lokomat device as an adjunct in improving gait, balance and quality of life in children with cerebral palsy.
Detailed Description
Background: Gait and balance have been a major issue faced by cerebral palsy children. Cerebral Palsy is the most common condition affecting around 2-2.5 children of 1000 live births (1 in every 400 children) over the last 20 years in the Western world (Levit, 2019). Cerebral Palsy causes complex issues related to physical, psychological and social functions. Active participation and the highest level of independence during daily living are primary goals for cerebral palsy children (Aurich, 2015). One of the major problems that limits activities of daily living is relate to gait and balance in cerebral palsy. From the past one-decade, the popularity of robotic assisted gait training devices have been increasing. There are a studies published on this topic from various parts of the globe and the results are mixed. Recent publications have demonstrated robotic assisted gait training benefits people with cerebral palsy, specifically in increasing walking speed and endurance (Carvalho, 2017). However, the efficacy of robotic assisted gait training in improving gait and balance is not well researched. This study will be the first one in the United Arab Emirates studying the local population and mainly focusing on functional aspects of gait, balance and quality of life.
Aims: The main aim is to investigate the effectiveness of robotic -assisted gait training as an adjunct to traditional physiotherapy to improve gait, balance and quality of life in children with cerebral palsy.
Research hypothesis: Robotic -assisted gait training applied as adjunct to traditional therapy could improve balance, walking and quality of life in children with cerebral palsy.
Methodology: The participants attending the outpatient clinic at Zayed Higher Organization for People of Determination, Abu Dhabi will be invited to take part in the study. They will be randomly allocated to two groups. This study proposes to have 50 participants with at least 25 in each group. The participants will all have spastic form of cerebral palsy as possible with the age of 4-18 years. All the participants will have to have be at Gross Motor Function Classification Level (GMFCS) level I- IV. The robotic -assisted gait training include 5 sessions per week, of 40 min long session during one-month period. The conventional physiotherapy includes 5 sessions per week of 40 min long session during one-month period. The primary analysis will be the pre to post-test differences of the Gross Motor Function Measure (GMFM-88),dimension D & E, 10 meters walk test, 6 minute walk test, Pediatric Balance Scale, Cerebral palsy Quality of Life questionnaire between experimental and control group.
Data analysis: Data will be statistically analysed using one-way anova. Descriptive statistics and graphic displays will be present for all outcomes for interventions comparing robotic -assisted gait training with traditional physiotherapy training.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
Children, Lokomat
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
41 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Robotic -assisted gait training group using Lokomat device
Arm Type
Experimental
Arm Description
5 sessions of 40 minutes of conventional therapy and
5 sessions of 40 minutes on Lokomat per week
Arm Title
Traditional therapy group
Arm Type
Active Comparator
Arm Description
• 5 sessions of 40 minutes of conventional therapy
Intervention Type
Device
Intervention Name(s)
Lokomat training
Other Intervention Name(s)
Conventional therapy
Intervention Description
Control group will receive the routine conventional physiotherapy treatment and the treatment for this group consists of the following:
Conventional therapy protocol:
5 sessions of 45 minutes a week, each session includes:
5 minutes of stretching exercise
20 minutes of strengthening exercise
10 minutes of balance exercise
10 minutes of gait training
Experimental group will receive 45 min of Lokomat in addition to the conventional approach (as explained above). Since Lokomat appointments can be only 8 per day, it is planned to have two groups of 8 participants for 4 weeks each. The Lokomat training include the following:
5 sessions of 45 minutes of conventional therapy (same as above) per week
5 sessions of 45 minutes on Lokomat per week
Primary Outcome Measure Information:
Title
Gross Motor Function Measure ( GMFM- 88) - dimension D & dimension E
Description
This is the validated test designed to measure change in gross motor function over time in children with cerebral palsy. Dimension D consist of 13 items for standing ability and dimension E has 24 items to assess walking, jumping and running in cerebral palsy children. Its a four point scoring system. Specific descriptors for each score is given in the Manual of GMFM-88.
Time Frame
Baseline time 0 and up to 8 weeks
Title
6 minute Walk test
Description
The test has been selected as a measure of gait endurance. This is validated test requiring individuals to walk 6 minutes on flat hard floor. Scoring is walking distance.
Time Frame
Baseline time 0 and up to 8 weeks
Title
10 meters Walk test
Description
The test has been selected as a measure of gait speed. This is validated test requiring individuals to walk on flat hard floor at their comfortable speed for 10 meters.
Time Frame
Baseline time 0 and up to 8 weeks
Title
Pediatric Balance Scale
Description
14 items valid scale is used to assess functional balance skills in children with spastic cerebral palsy.
Time Frame
Baseline time 0 and up to 8 weeks
Title
Cerebral Palsy Quality of Life questionnaire for child (CP QOL-child) and Cerebral Palsy Quality of Life questionnaire for adolescent (CP QOL- teen)
Description
This Arabic validated CP QOL- child for age 4-12 and CP QOL- teen for age 13-18 questionnaires are used in the parent version. Its assesses 7 domains on a 9 level point Likert scale.
Time Frame
Baseline time 0 and up to 8 weeks
Secondary Outcome Measure Information:
Title
Range of motion
Description
Measuring range of motion in hip, knee, ankle joint using the reliable tool called goniometer.
Time Frame
Baseline time 0 and up to 8 weeks
Title
The Oxford scale
Description
The most commonly used scale for testing muscle strength.
Time Frame
Baseline time 0 and up to 8 weeks
Title
Modified Ashworth Scale
Description
It is a muscle tone assessment.
Time Frame
Baseline time 0 and up to 8 weeks
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 with spastic and mix form
Gross Motor Function Classification System (GMFCS from level II to IV)
Age 4 to 18
No contraindications for the training in the Lokomat
Able to follow simple instructions
Exclusion Criteria:
On botox injection within the last 6 months (as the effect of botox wear out in 6 months)
Surgery within the last one year
Fixed contractures and/or with bone instability
Baclofen infusion pumps in situ
Seizure disorder that is not controlled by medication (if on medication, must not have had a seizure in the last 12 months);
Open skin lesions or vascular disorder of lower extremities;
Having participated in another Lokomat training regime within the previous 3months as well as a change in concomitant treatment within the last 4 weeks before or during the study period
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dragana Djuric
Organizational Affiliation
FCHS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fatima College of Health Sciences
City
Abu Dhabi
ZIP/Postal Code
3758
Country
United Arab Emirates
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Effectiveness of Robotic Assisted Gait Training as an Adjunct to Traditional Physiotherapy in Cerebral Palsy
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