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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT00356343
Other study ID # R01HD043859
Secondary ID
Status Active, not recruiting
Phase Phase 1
First received July 25, 2006
Last updated January 9, 2011
Start date July 2004

Study information

Verified date January 2011
Source Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if using high-intensity, short-duration, intermittent neuromuscular electrical stimulation (NMES) is better than volitional exercise in increasing quadriceps femoris and triceps surae force-generating potential and gross motor function in children with cerebral palsy.


Description:

The overall goal of this study is to determine if using high-intensity, short-duration, intermittent neuromuscular electrical stimulation (NMES) is better than volitional exercise in increasing quadriceps femoris and triceps surae force-generating potential and gross motor function in children with cerebral palsy. This study consists of a randomized controlled trial in which the effects of NMES applied to the quadriceps femoris and triceps surae are compared to the effects of volitional isometric exercise and a non-exercising control group. This project assesses the ability of NMES to increase muscle force generating ability, the mechanisms behind changes in force generating ability, and the effects of training on spatiotemporal parameters of gait and gross motor function in children with cerebral palsy.

Subjects is the NMES group will be implanted with percutaneous electrodes in the medial and lateral heads of the gastrocnemius and the quadriceps (3 electrodes in each lower extremity, implanted bilaterally). During the intervention phase, these subjects will undergo 15 electrically-elicited contractions in each of the implanted muscle groups three times/week (at home), while positioned on an exercise board to maintain good alignment and facilitate isometric contractions. Subjects in the volitional group will perform 15 isometric contractions in each muscle group (quadriceps, triceps surae), while positioned on an exercise board. The non-exercise control group will continue with typical activities, but no intervention will be administered. Subjects are assessed at baseline, 6 weeks into the intervention, 12 weeks into the intervention (at which point the intervention is withdrawn), and at a follow-up assessment 12 weeks after the withdrawal of the intervention.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 45
Est. completion date
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 7 Years to 12 Years
Eligibility Inclusion Criteria:

- Children ages 7-12 years old

- Diagnosis of spastic diplegic cerebral palsy

- GMFCS level of II or III (able to walk indoors and outdoors with or without an assistive device)

- PROM requirements (<10 degree hip flexion contracture, >20 degrees of hip abduction, < 5 degrees of knee flexion contracture, > 45 degree popliteal angle, ankle dorsiflexion to neutral with knee extension)

- Sufficient cognitive/communication skills to perform volitional muscle contractions and complete data collection procedures

Exclusion Criteria:

- Significant orthopedic impairments (hip MIGR > 40%, significant scoliosis)

- Must be at least one year post orthopedic surgery

- Must be at least 6 months post botulinum toxin injections

- Uncontrolled seizure activity

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
NMES Strength Training
Subjects will complete 12 weeks of NMES isometric strength training using implanted electrodes in bilateral quadriceps and triceps surae muscles.
Other:
Volitional Strength Training
Subjects will complete 12 weeks of volitional isometric strength training of bilateral quadriceps and triceps surae muscles.

Locations

Country Name City State
United States Shriners Hospitals for Children, Philadelphia Philadelphia Pennsylvania

Sponsors (3)

Lead Sponsor Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Shriners Hospitals for Children, University of Delaware

Country where clinical trial is conducted

United States, 

References & Publications (1)

Stackhouse SK, Binder-Macleod SA, Lee SC. Voluntary muscle activation, contractile properties, and fatigability in children with and without cerebral palsy. Muscle Nerve. 2005 May;31(5):594-601. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Force generating ability of quadriceps femoris and triceps surae (MVIC) Pre, Mid, Post, Washout No
Primary Voluntary muscle activation during a Maximal Volitional Isometric Contraction (MVIC) Pre, Mid, Post, Washout No
Primary Antagonist coactivation during an agonist MVIC Pre, Mid, Post, Washout No
Primary Contractile properties as assessed via electrically-elicited tests Pre, Mid, Post, Washout No
Primary Fatiguability of muscle as assessed via electrically-elicited tests Pre, Mid, Post, Washout No
Primary Muscle cross-sectional area of quadriceps femoris and triceps surae (via MRI with fat suppression) Pre, Mid, Post, Washout No
Primary Spatiotemporal parameters of gait Pre, Mid, Post, Washout No
Primary Gross Motor Function Measure Pre, Mid, Post, Washout No
Primary Timed Up and Go Pre, Mid, Post, Washout No
Primary Parent and child report via questionnaires (PODCI, COPM) Pre, Mid, Post, Washout No
See also
  Status Clinical Trial Phase
Completed NCT00401154 - Study of a Stationary Cycling Intervention for Children With Spastic Diplegic Cerebral Palsy N/A
Enrolling by invitation NCT06218316 - Repetitive Transcranial Magnetic Stimulation Versus Botulinum Injection on Spasticity on Children With Diplegic Cerebral Palsy N/A
Not yet recruiting NCT04177186 - Strength Training in Children With Spastic Diplegic and Hemiplegic Cerebral Palsy Receiving Botulinum Toxin N/A
Completed NCT00261131 - Efficacy and Functional Outcomes of Botulinum Toxin A Injections to Hamstrings in Flexed Knee Gait in Cerebral Palsy Phase 3
Completed NCT00255073 - Does Reducing Spasticity Permit an Increase in Strength? Phase 2
Recruiting NCT05504798 - A New Multimodal Treatment Approach for Children With Spastic Diplegic Cerebral Palsy N/A

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