Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders

Cerebral Palsy Clinical Trial

Official title: Evaluating an Extension Assist Knee Ankle Foot Orthosis to Improve Gait in Children With Movement Disorders

Status Recruiting

Clinical Trial Summary

Background:

• Cerebral palsy (CP) is the most common motor disorder in children. CP often causes crouch gait, an abnormal way of walking. Knee crouch has many causes, so no single device or approach works best for everybody. This study s adjustable brace provides many types of walking assistance. Researchers will evaluate brace options to find the best solution for each participant, and whether one solution works best for the group.

Objective:

• To evaluate a new brace to improve crouch gait in children with CP.

Eligibility:

• Children 5 17 years old with CP.

• Healthy volunteers 5 17 years old.

Design:

• All participants will be screened with medical history and physical exam.

• Healthy volunteers will have 1 visit. They will do motion analysis, EMG, and EEG described below.

• Participants with CP will have 6 visits.

• Visit 1:

<TAB>1. Motion analysis: Balls will be taped to participants skin. This helps cameras follow their movement.

<TAB>2. EMG: Metal discs will be taped to participants skin. They measure electrical muscle activity.

<TAB>3. Participants knee movement will be tested.

<TAB>4. Participants will walk 50 meters.

<TAB>5. Participants legs will be cast to make custom braces.

• Visit 2:

• Participants will wear their new braces and have them adjusted.

• Steps 1 3 will be repeated.

• EEG: Small metal discs will be placed on the participants scalp. They record brain waves.

• Participants will have electrical stimulation of their knees and practice extending them.

• Participants will take several walks with the braces in different settings.

• Visits 3 5: participants will repeat the walking and some other steps from visit 2.

• Visit 6 will repeat visit 2.

Clinical Trial Description

Objective

The purpose of this protocol is to evaluate several configurations of a prototype Extension Assist Knee-Ankle-Foot Orthosis (EA-KAFO) in patients with cerebral palsy (CP), muscular dystrophy (MD), spina bifida (SB), or incomplete spinal cord injury (iSCI) who have knee extension deficiency. Three forms of assistance will be provided at the knee joint including a passive-damper component, functional electrical stimulation (FES) to the quadriceps, and a motorized assist. One form will provide controllable resistance at the knee to strengthen muscles and promote knee extension after the resistance is removed. These will be compared to traditional bracing which typically improves crouch by blocking some or all motion at one or both joints. We hypothesize that all assistive configurations will improve gait alignment and performance compared to the non-assisted conditions. We further hypothesize that a best solution for each participant will exist, but may vary across subjects due to the heterogeneity of these movement disorders. Preliminary data on brain activation using EEG will be collected during all walking conditions.

Study population

Thirty (30) subjects, age 5 and above, diagnosed with crouch gait from diplegic CP, (30) subjects, age 5 and above, with knee extension deficiency from MD, SB, or iSCI (15 from each group) and 10 age-matched healthy volunteers will be recruited.

Design

This protocol will evaluate an EA-KAFO prototype consisting of a custom fabricated brace combined with a modular knee joint with three modes of operation: hinge (no assist), a passive spring-damper, and an active motorized assist. Since crouch can also be precipitated at the ankle, the orthotic ankle joint has an adjustable dynamic resistance (ADR) mechanism that can be locked (passive assist) to simulate a standard brace, free, or provide variable resistance to assist knee extension. Additionally, we will combine quadriceps FES with the hinge and the passive damper to create two hybrid configurations. The hinge and the passive damper (Ultraflex ) knee modules, and ADR ankle brace are FDA-approved (Class I), commercially available devices. This protocol for evaluation of the active motorized joint module, the two hybrid configurations, and the controllable resistance device (PowerWalk by Agilik Technologies) has been reviewed by the FDA as a medical device study and was determined by the FDA to be non-significant risk. Healthy controls will come for one visit, and participants with movement disorders will complete 6-10 visits: 1) initial assessment and casting for custom leg brace; 2) EA-KAFO configuration; 3) initial data collection and practice; 4-5) accommodation to brace configurations; 6) final data collection. Additional accommodation visits may be added if necessary, up to the maximum of 10 total visits. Participants with movement disorders will be permitted to re-enroll in the protocol is a minimum of 1 year has passed from their prior final visit. Motion capture, force plates, and electromyography (EMG) will be used for gait analysis while electroencephalography (EEG) will measure brain activity during walking.

Outcome measures

The primary outcome is the amount of knee flexion during gait. The optimal solution for each individual will be that which provides the greatest reduction in peak knee angle. Secondary outcomes will include gait speed, knee extensor moment, and EEG activation profiles. ;

Related Conditions & MeSH terms

• Cerebral Palsy
• Incomplete Spinal Cord Injury
• Movement Disorders
• Muscular Dystrophies
• Muscular Dystrophy
• Spina Bifida
• Spinal Cord Injuries
• Spinal Dysraphism

• NCT number: NCT01961557
• Study type: Interventional
• Source: National Institutes of Health Clinical Center (CC)
• Contact: Jesse H Matsubara
• Phone: (301) 451-7530
• Email: jesse.matsubara@nih.gov
• Status: Recruiting
• Phase: N/A
• Start date: July 2, 2015
• Completion date: December 31, 2025