RECRUITING

Improving Neck Control in Children With Cerebral Palsy Using Robotics

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Promoting Functional Neck Motion in Patients With Cerebral Palsy Using a Dynamic Neck Brace

Quick Facts

Study Start:2025-03-06
Study Completion:2026-12-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06533293

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:11 Years to 21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * CP, as medical diagnosis
  2. * GMFCS IV-V classification
  1. * severe cognitive deficits
  2. * uncontrolled epilepsy
  3. * severe dyskinesia
  4. * spinal cord malformations
  5. * severe vertebral column deformities (scoliosis \>40° and/or kyphosis \>45º)
  6. * blindness
  7. * chemo-denervation 3 months before study

Contacts and Locations

Study Contact

Sunil K Agrawal, PhD
CONTACT
2128542841
sunil.agrawal@columbia.edu
Victor Santamaria
CONTACT
vsantama@nymc.edu

Principal Investigator

Sunil Agrawal
PRINCIPAL_INVESTIGATOR
Columbia University

Study Locations (Sites)

ROAR Lab, Mudd Hall
New York, New York, 10027
United States
Columbia University Irving Medical Center
New York, New York, 10032
United States

Collaborators and Investigators

Sponsor: Columbia University

  • Sunil Agrawal, PRINCIPAL_INVESTIGATOR, Columbia University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-03-06
Study Completion Date2026-12-30

Study Record Updates

Study Start Date2025-03-06
Study Completion Date2026-12-30

Terms related to this study

Keywords Provided by Researchers

  • Motor training, Robotics

Additional Relevant MeSH Terms

  • Cerebral Palsy
  • Neck Disorder