Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06226493

EEG Changes and DNA Markers Related to taVNS in Stroke Patients: a Preliminary Study

Led by Casa Colina Hospital and Centers for Healthcare · Updated on 2026-03-31

44

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

Sponsors

C

Casa Colina Hospital and Centers for Healthcare

Lead Sponsor

F

Foundation for Physical Medicine and Rehabilitation

Collaborating Sponsor

AI-Summary

What this Trial Is About

In the United States, more than 795,000 people have a stroke every year. Motor impairment after a stroke is common and can be debilitating. To date, there remain few treatments available to help improve motor recovery after a stroke, making this an important area of research. Novel use of neuromodulation such as Invasive Vagus Nerve Stimulation (VNS) has been shown to improve motor recovery in stroke patients. Vagus nerve stimulation (VNS), in which the nerve is stimulated with electrical pulses, has demonstrated success for a variety of conditions, including inflammation, depression, cognitive dysfunction, chronic fatigue, headaches/migraines, pain, insomnia, and cardiovascular issues. Very recently, non-invasive options have been developed and might be a promising alternative. The research in this area is still very limited and much more research is needed to investigate non-invasive/trancutaneous auricular vagus nerve stimulation (taVNS) related biomechanisms and to further support its efficacy in acute patients. The purpose of this study is to build upon the current research to investigate changes in electrical brain activity (using electrophysiology) and genetic markers related to improvements in both motor and cognitive recovery following the use of taVNS vs. sham in acute stroke patients.

CONDITIONS

Official Title

EEG Changes and DNA Markers Related to taVNS in Stroke Patients: a Preliminary Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • First-time Cerebrovascular Accident (Ischemic or Hemorrhagic)
  • Within a month post-injury
  • Presence of motor impairments (FMA-U�3c=62)
Not Eligible

You will not qualify if you...

  • Advanced cardiac, pulmonary, liver, or kidney disease
  • Bradycardia (Resting HR < 60)
  • Presence of Apraxia, Aphasia or confusion
  • Other musculoskeletal or neurologic diseases that could interfere with the outcome measures
  • Previous surgical intervention on the vagus nerve
  • Participation in other clinical trials
  • Alcohol or drug abuse

AI-Screening

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Trial Site Locations

Total: 1 location

1

Casa Colina Hospital and Centers for Healthcare

Pomona, California, United States, 91769

Actively Recruiting

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Research Team

C

Caroline Schnakers, PhD

CONTACT

N

Niko Fullmer, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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