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Clinical Trials/NCT05131724
NCT05131724
Not yet recruiting
Not Applicable

Effectiveness of Virtual Reality on Functional Mobility During Treadmill Training in Children With Cerebral Palsy: a Randomized Clinical Trial (VirtWalkCP Project)

University of Vic - Central University of Catalonia1 site in 1 country30 target enrollmentSeptember 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy, Spastic
Sponsor
University of Vic - Central University of Catalonia
Enrollment
30
Locations
1
Primary Endpoint
Functional mobility change
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

Cerebral palsy (CP), which occurs as a consequence of brain damage, has multiple deficits such as a global reduction of motor cortical activity during movement execution and inadequate processing of corticospinal and somatosensory circuits. Global registers estimate that it occurs in two to three of 1.000 live births, and spasticity is the most common disorder, occurring in 80% of children with CP. Spasticity might affect both upper and lower limbs, resulting in other deficits in joint mobility, postural reactions, selective motor control, balance, and gait. This set of impairments and deficits may lead to limitations in functional ability and autonomy in the performance of daily living activities, physical fitness, quality of life, and/or ability to participate in games and sports activities compared to neurotypical peers of the same age.

Walking is considered one of the most important activities in daily life, as it is essential for activities of daily living and social participation. Children with Gross Motor Function Classification System (GMFCS) levels I, II, and III show potential for walking, and around 75% of CP children are ambulatory. However, abnormalities in neural control and muscle weakness contribute to several gait characteristics such as slow velocity, decreased stride length, increased stance phase percentage, and increased peak ankle dorsiflexion and knee flexion, and peak hip extension moments. Consequently, this gait pattern contributes to postural instability and increased fall risk in children with CP, among others.

Detailed Description

The main objective of the present study is to evaluate the effectiveness of treadmill gait training and virtual reality comparing to treadmill gait training on functional mobility in infants with spastic cerebral palsy. The study design is a two-arm randomized clinical trial, single-center and single-blind (evaluators). The sample will be recruited at the Hospital General de Vic, and the study will be conducted at the Universitat de Vic - Universitat Central de Catalunya (UVic-UCC).

Registry
clinicaltrials.gov
Start Date
September 2022
End Date
September 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University of Vic - Central University of Catalonia
Responsible Party
Principal Investigator
Principal Investigator

Mirari Ochandorena Acha

Associate professor

University of Vic - Central University of Catalonia

Eligibility Criteria

Inclusion Criteria

  • Medical diagnosis of spastic cerebral palsy
  • Motor function levels I to III according to the Gross Motor Function Classification System
  • Independent walking was acquired for more than 12 months.
  • Able to ambulate for at least 10 meters with or without aids.

Exclusion Criteria

  • Orthopaedic surgery on the lower limbs in the past 12 months.
  • Scheduled surgery during the period of the study.
  • Orthopaedic deformities with surgery indication.
  • Uncontrolled seizure disorder.
  • Metallic implant in the skull.
  • Hearing aid.
  • Have received toxic botulin injections in the past 6 months.
  • Significant cognitive or visual impairment.

Outcomes

Primary Outcomes

Functional mobility change

Time Frame: Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks).

The 6-Minute Walk Test (6MWT) will be performed according to the recommendations. The test will be performed once in a 10m course layout. Participants will receive standardized instructions and encouragement. The test-retest interclass correlation coefficient of this test is 0.98. The estimated time to perform the test is 10 minutes.

Secondary Outcomes

  • Static balance(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Walking speed(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Dynamic balance(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Gross motor function(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Functional independence(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Health-related quality of life(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))
  • Occupational participation(Basal assessment, at the end of the intervention (an average of 3 weeks), 1 month after the end of the intervention (an average of 8 weeks))

Study Sites (1)

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