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Balance Control in Children With Cerebral Palsy

Sensor Fusion for Balance Control in Children With Cerebral Palsy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02456376
Enrollment
20
Registered
2015-05-28
Start date
2014-05-31
Completion date
2016-12-31
Last updated
2015-05-28

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

Conditions

Cerebral Palsy

Keywords

Sensor Fusion, Stochastic Resonance Stimulation, Sensory deficits, Postural Control

Brief summary

The purpose of this study is to investigate how sensory information processing affects balance ability in children with cerebral palsy (CP). An additional goal is to determine if a subsensory electrical stimulation called Stochastic Resonance (SR) Stimulation, can improve balance in children with CP. Children with CP and children with typical development will participate and complete a series of clinical and balance assessments. They will also be tested in a sensor fusion paradigm to investigate potential deficits in the dynamic integration of visual, vestibular and proprioceptive information during upright stance. SR stimulation will then be used to potentially improve these deficits and subsequently their balance ability.

Interventions

PROCEDURESensory Integration Testing

Investigate how sensory information are integrated during upright stance when visual and body senses are challenged in a virtual reality environment

PROCEDURESR stimulation & Sensory integration testing

Use SR stimulation to improve sensory integration when visual and body senses are challenged in a virtual reality environment

Sponsors

Shriners Hospitals for Children
CollaboratorOTHER
University of Delaware
CollaboratorOTHER
Temple University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of spastic diplegia CP (GMFCS I- III)\* * Ability to stand independently for approximately 2 min

Exclusion criteria

* Lower extremity surgery or fractures in the year prior testing * Joint instability or dislocation in the lower extremities * Botulinum toxin injections in the lower extremities within the past 6 months\* * Marked visual or hearing deficits * Uncontrolled seizure disorder * Implanted medical device that may be contraindicated with application of SR stimulation * Asterisk indicates the eligibility criteria that should be met only by children with CP

Design outcomes

Primary

MeasureTime frameDescription
Gain response1 dayFor both the sensory reweighting testing, the visual signal will be displayed as a visual flow with translation in anterior-posterior (AP) direction (i.e., sagittal plane) and presented at different amplitudes (0.25 and 0.5 cm) at 0.2 Hz to measure: the change in gain (weighting) to vision (intramodal effect); and a change in gain to vibration and galvanic stimulation (intermodal effects). Gain for each modality relative to both the leg segment AP translation and trunk segment AP translation will be measured.

Secondary

MeasureTime frameDescription
Gain response1 dayFor the sensory reweighting with the addition of SR stimulation testing, the visual signal will be displayed as a visual flow with translation in anterior-posterior (AP) direction (i.e., sagittal plane) and presented at different amplitudes (0.25 and 0.5 cm) at 0.2 Hz to measure: the change in gain (weighting) to vision (intramodal effect); and a change in gain to vibration and galvanic stimulation (intermodal effects). Gain for each modality relative to both the leg segment AP translation and trunk segment AP translation will be measured.

Countries

United States

Contacts

Primary ContactAnastasia Zarkou, PT, MS
azarkou@udel.edu
Backup ContactSamuel CK Lee, PT, PhD
slee@udel.edu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026