Actively Recruiting

Phase Not Applicable
Age: 8Years - 17Years
All Genders
NCT07390760

Remote Ischemic Conditioning and Spinal Reflex Modulation in Children With Cerebral Palsy

Led by East Carolina University · Updated on 2026-03-24

16

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Remote ischemic conditioning (RIC) is a clinically feasible intervention involving brief, sublethal periods of ischemia followed by reperfusion that has been shown to enhance motor performance, strength, and balance when combined with training in healthy adults and individuals with neurological conditions. Although RIC is thought to influence neuroplasticity through neural, metabolic, and humoral pathways, its effects on spinal-level mechanisms remain poorly understood. Emerging evidence indicates that neuroplastic adaptations occur not only at the cortical level but also within the spinal cord. Moreover, altered spinal reflex excitability is associated with spasticity, balance impairments, and functional limitations in children with cerebral palsy (CP), yet the role of spinal reflex modulations in response to RIC and balance training remains under expplored in this population. Therefore, this study aims to investigate the effects of RIC combined with balance training on spinal reflex modulation in children with CP.

CONDITIONS

Official Title

Remote Ischemic Conditioning and Spinal Reflex Modulation in Children With Cerebral Palsy

Who Can Participate

Age: 8Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children diagnosed with cerebral palsy between 8 and 17 years old
  • Gross motor function classification system levels I to III
  • Enrolled in mainstream school with sufficient cognition to follow study instructions
Not Eligible

You will not qualify if you...

  • Other developmental disabilities such as autism or developmental coordination disorders
  • Significant cognitive deficits affecting understanding or communication
  • Balance disorders including vestibular disorders or posterior fossa tumor
  • Known cardiorespiratory dysfunctions
  • Sickle cell disease
  • Receiving other adjunct therapies like transcranial magnetic stimulation or vagal nerve stimulation
  • Lower extremity condition, injury, or surgery within the last three months
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

East Carolina University

Greenville, North Carolina, United States, 27834

Actively Recruiting

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Research Team

S

Swati M Surkar, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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