Actively Recruiting

Phase Not Applicable
Age: 11Years - 21Years
All Genders
Healthy Volunteers
NCT06533293

Improving Neck Control in Children With Cerebral Palsy Using Robotics

Led by Columbia University · Updated on 2025-09-09

30

Participants Needed

2

Research Sites

94 weeks

Total Duration

On this page

Sponsors

C

Columbia University

Lead Sponsor

N

New York Medical College

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this study is to characterize the head-neck motion of children with cerebral palsy and investigate how robotics can be used to improve the head-neck coordination of these children. Aim 1 is a cross-sectional study. In this single-session, kinematic and muscle activity data will be collected during the postural static, active-proactive, and reactive postural head tasks. Gross Motor Functional Classification System (GMFCS) levels will also be collected to categorize the sample into subgroups. Aim 2 is a prospective cohort quasi-experimental study. The data will be collected at baseline, across 12 intervention sessions, 1 week post-intervention, and 3 months follow-up. Functional assessments will be used to compare across the pre, mid, and post training. Participants will be assessed in Gross Motor Functional Measures (GMFM), Seated Posture and Reaching Control (SP\&R-co), and Canadian Occupational and Performance Measure (COPM). The primary outcomes will be SP\&R-co test and COPM pre- and post-intervention.

CONDITIONS

Official Title

Improving Neck Control in Children With Cerebral Palsy Using Robotics

Who Can Participate

Age: 11Years - 21Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with cerebral palsy
  • Classified as GMFCS level IV or V
  • Aged between 11 and 21 years
Not Eligible

You will not qualify if you...

  • Severe cognitive deficits
  • Uncontrolled epilepsy
  • Severe dyskinesia
  • Spinal cord malformations
  • Severe vertebral column deformities (scoliosis >40° and/or kyphosis >45°)
  • Blindness
  • Received chemo-denervation within 3 months before the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

ROAR Lab, Mudd Hall

New York, New York, United States, 10027

Actively Recruiting

2

Columbia University Irving Medical Center

New York, New York, United States, 10032

Not Yet Recruiting

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Research Team

S

Sunil K Agrawal, PhD

CONTACT

V

Victor Santamaria

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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