Improving Neck Control in Children With Cerebral Palsy Using Robotics

This study is looking for children and young adults aged 11 to 21 with Cerebral Palsy (CP) to test a new robotic neck brace device. The device, made at Columbia University, measures head movement and muscle activity, and uses springs and motors to support and assist head movement. The goal is to understand how children with CP move their head and neck, and to see if this robotic device can help improve their head and neck control. Researchers will measure your seated posture and ability to reach to see if the device is successful. The study is currently unclear on its recruitment status and plans to enroll 30 participants.

Study design
This study is interventional and plans to enroll 30 participants. It includes a cross-sectional study and a prospective cohort quasi-experimental study.
What's involved
You would participate in a single session for the first part of the study, and then in 12 intervention sessions for the second part.
Compensation
Not stated in the trial record.
Follow-up
Your progress will be checked immediately after the intervention, one week later, and then again three months after the intervention.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06533293

Improving Neck Control in Children With Cerebral Palsy Using Robotics

Recruiting
NAAges 11–21InterventionalTreatment
Columbia University
~30 participants
Updated 2025-09-09 on ClinicalTrials.gov
What's tested:Neck Brace Device

At a glance

Recruiting sites
1 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Seated Postural and Reaching Control (SP&R-co)
Measured over Data will be collected at baseline, immediately after post-intervention, 1 week post-intervention, and 3 months follow-up.
Cerebral Palsy
Neck Disorder
2 sites across 1 states
New York2
  • Sunil Agrawal · PRINCIPAL_INVESTIGATOR · Columbia University

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

CP, as medical diagnosis
GMFCS IV-V classification

Exclusion

severe cognitive deficits
uncontrolled epilepsy
severe dyskinesia
spinal cord malformations
severe vertebral column deformities (scoliosis \>40° and/or kyphosis \>45º)
blindness
chemo-denervation 3 months before study
  • Seated Postural and Reaching Control (SP&R-co)Data will be collected at baseline, immediately after post-intervention, 1 week post-intervention, and 3 months follow-up.

    Measurement of head-trunk and reaching control of children and young adults with CP while sitting static, active, proactive, and reactive postural dimensions while providing support at different regions of the torso.