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Clinical Trials/NCT05540990
NCT05540990
Completed
Not Applicable

The Effectiveness of Robot Assisted Gait Training In Children With Cerebral Palsy: Randomized Comparative Trial

Ankara University1 site in 1 country57 target enrollmentSeptember 15, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy
Sponsor
Ankara University
Enrollment
57
Locations
1
Primary Endpoint
Change in GMFM-88 D Item
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Cerebral Palsy (CP) is considered a neurological disorder caused by a non-progressive brain injury or malformation that occurs while the child's brain is under development. CP primarily affects body movement and muscle coordination. Robot assisted gait training (RAGT) is considered to be a promising approach for improving gait related gross motor function of children and youth with CP.

There is weak and inconsistent evidence regarding the use of RAGT for children with gait disorders. Further research is required with increased numbers and with relevant outcome measures to both confirm the effectiveness and clarify training schedules.

The aim of this research project is to investigate the effectiveness of robot assisted gait training on improvements of functional gait parameters in children with cerebral palsy.

Detailed Description

Cerebral Palsy (CP) is a disorder of posture and movement due to a defect in the immature brain. There is evidence that locomotor therapy for regaining walking capacity using the principle of enhancing neuroplasticity by task-specific training is effective in the rehabilitation process of patients with central gait disorders. The use of a robotic device assists in achieving and maintaining physiological walking pattern for extended periods of therapy. The use of robotic devices as an alternative treatment to improve the gait function in patients with CP has increased. This is a prospective, randomized comparative trial (RCT). This study is designed to compare the effectiveness of conventional physical therapy (CPt) and robot assisted gait training (RAGT) on gait related motor skills of children with cerebral palsy. Children aged 5 to 18 years with GMFCS Level 2-4, bilateral or unilateral spastic CP are accepted into this study. Participants are randomly assigned to receive CPt or RAGT + CPt. All two intervention groups will receive 2-3 sessions of CPt per week over 6-8 weeks. CPt sessions are individually customized to the needs of the child. The participants of RAGT + CPt group also receive 15 sessions of RAGT (2-3 times per week with a maximum of 45 minute each).

Registry
clinicaltrials.gov
Start Date
September 15, 2022
End Date
July 26, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Birkan Sonel Tur

Clinical Professor

Ankara University

Eligibility Criteria

Inclusion Criteria

  • GMFCS Level 2-4
  • Bilateral or unilateral spastic CP
  • Able to follow instructions and communicate pain or discomfort
  • Have a passive range of motion (ROM) of hips and knees within minimum range requirement for robotic assisted training (hip and knee flexion contracture ≤10°, and knee valgus ≤40°)
  • Not having participated in another robotic assisted training regime within the previous 6 months
  • Able to participate in a minimum of 30 minutes robotic assisted training session
  • Able to commit to attendance of two to three times weekly for 15 sessions (to support the primary efficacy analysis)

Exclusion Criteria

  • Botulinum toxin type A injection within 3 months
  • Orthopedic surgery on the lower extremity (muscle surgery within the last 9 months, bone surgery within 12 months)
  • Bone fractures, open skin lesions, or circulatory problems
  • Vision and hearing impairments that affect participation in robotic assisted training
  • Epilepsy resistant to medication
  • Cardiopulmonary instability
  • Use of a baclofen pump

Outcomes

Primary Outcomes

Change in GMFM-88 D Item

Time Frame: baseline, 8 weeks, 14 weeks and 20 weeks

The Gross Motor Function Measure (GMFM) is an assessment tool designed and evaluated to measure changes in gross motor function over time or with intervention in children with cerebral palsy. GMFM-88 is a measure developed to evaluate the gross motor function changes in CP children. It has five components: lying and rolling, sitting, kneeling and crawling, standing, and walking. D dimension is for Standing abilities. The score of each dimension is expressed as a percentage of the maximum score. There is a scoring system with each item scored as 0, 1, 2, 3, or "not tested". A scoring key of 0 - does not initiate, 1 - initiates, 2 - partially completes, and 3 - completed, is used. It takes between 20-25 minutes to be completed.

Change in GMFM-88 E Item

Time Frame: baseline, 8 weeks, 14 weeks and 20 weeks

The Gross Motor Function Measure (GMFM) is an assessment tool designed and evaluated to measure changes in gross motor function over time or with intervention in children with cerebral palsy. GMFM-88 is a measure developed to evaluate the gross motor function changes in CP children. It has five components: lying and rolling, sitting, kneeling and crawling, standing, and walking. E dimension is for Walking, Running \& Jumping abilities. The score of each dimension is expressed as a percentage of the maximum score. There is a scoring system with each item scored as 0, 1, 2, 3, or "not tested". A scoring key of 0 - does not initiate, 1 - initiates, 2 - partially completes, and 3 - completed, is used. It takes between 20-25 minutes to be completed.

Secondary Outcomes

  • Change in Pediatric Quality of Life Inventory (PedsQL) 3.0 Cerebral Palsy Module (Parent Form)(baseline, 8 weeks, 14 weeks and 20 weeks)
  • Change in 6 Minute Walk Test(baseline, 8 weeks, 14 weeks and 20 weeks)
  • Change in 10 Meter Walk Test(baseline, 8 weeks, 14 weeks and 20 weeks)
  • Change in Modified Ashworth Scale(baseline, 8 weeks, 14 weeks and 20 weeks)
  • Change in Goal Attainment Scale (GAS)(baseline, 8 weeks, 14 weeks and 20 weeks)

Study Sites (1)

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