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Effectiveness of a Treatment With the Robot - Assisted Gait Training System Walkbot in Patients With Cerebral Palsy

Effectiveness of a Treatment With the Robot - Assisted Gait Training System Walkbot in Patients With Cerebral Palsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04329793
Enrollment
23
Registered
2020-04-01
Start date
2019-04-08
Completion date
2021-03-14
Last updated
2021-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy

Brief summary

The improvement of walking capacity is a key objective of the rehabilitation of children with PC. There are different approaches from physiotherapy to address this need, including walking on the ground and on treadmill with partial weight support. Currently, there are robotic technologies adapted to the functional rehabilitation of patients. Assisted gait training with robotic devices such as the Walkbot allows a longer duration of training, at more variable speeds, and with a constant gait pattern adapted to the patient. This training, based on the intensity and repetition of the movement, has beneficial effects on the recovery and improvement of the patient's postural and locomotor functions. There are some studies that evaluate walking interventions on treadmill with partial weight support, on the ground and in assisted walking robot in patients with PC. Currently, there are no studies conducted that report the effectiveness of interventions performed with robotic walking training device Walkbot K on PC. However, studies in adults with Walkbot S, affected with neurological injury, have reported good results. Assisted gait training with robotic devices such as the Walkbot, based on the intensity and repetition of the movement, has beneficial effects on the recovery and improvement of the patient's postural and locomotor functions. However, due to the little evidence that exists, it is necessary to know the effectiveness of the Walkbot assisted walking robot in these patients by means of a clinical trial that allows to firmly establish the scope of its benefits.

Interventions

DEVICEAssisted gait training with Walkbot System

The experimental group will receive at least 3 treatment sessions per week consisting of 40 minutes in robot-assisted gait training with Walkbot System in addition to their usual Physical therapy sessions. In total, the number of Walkbot sessions will be 20, in uninterrupted weeks.

OTHERPhysical Therapy

The control group will receive their usual Physical therapy sessions during 6 weeks.

Sponsors

Universidad de Murcia
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* Cerebral palsy diagnosis (diplegia or tetraplegia) * Ability to communicate even if not verbal (yes/not; gestures; pictograms; sounds) * Levels II, III and IV in GMFCS * Unsupported seating capacity * Go on standing with or without help * Not receiving therapy with a walking robot and not having received it in at least one year

Exclusion criteria

* Serious psychiatric problems * Serious heart problems * Active tumors * Severe joint degenerative problems * Degenerative diseases of the nervous system * Mitochondrial diseases * Recent surgeries * Unbound fractures * Severe osteoporosis * Uncontrolled seizures * Open wounds in the lower half of the body * Extreme fear of being placed in robotic devices * Anthropomorphic measures are below the minimum required to use the device

Design outcomes

Primary

MeasureTime frameDescription
Ability and quality of walking.Baseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionChanges in Gross Motor Function Measure-88 (dimensions IV y V)

Secondary

MeasureTime frameDescription
Muscle strengthBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionDifferences in muscle strength of lower limbs, measured with dynamometer.
Range of motionBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionAnalyze if the range of joint mobility is increased in those joints that are more limited, measured with goniometer.
Functionality and autonomyBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionDifferences in the basic activities of daily life, measured with the PedsQL- Cerebral Palsy Module
Quality of walking: Edinburgh Visual Gait ScaleBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionChanges in Edinburgh Visual Gait Scale values. Higher scores mean worse outcome. Minimum value is 0. Maximum value is 34.
Gait enduranceBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionChanges in 6 minutes walk test
SpasticityBaseline, immediately after the intervention, 1 month after the intervention, 3 months after the interventionChanges in spasticity values, measured with the modified Ashworth Scale. Higher scores mean worse outcome. Minimum value is 0. Maximum value is 4.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026