Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT03317860

Improving Measurement and Treatment of Post-stroke Neglect

Led by VA Office of Research and Development · Updated on 2025-09-17

17

Participants Needed

1

Research Sites

430 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study examines how to best assess and treat post-stroke neglect. This study will examine the preliminary effects of an innovative intervention (repetitive task-specific practice + transcranial direct current stimulation) for individuals with neglect. This study will also determine whether items from various neglect assessments can be combined to establish a more comprehensive neglect measure.

CONDITIONS

Official Title

Improving Measurement and Treatment of Post-stroke Neglect

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ischemic or hemorrhagic stroke at least 3 months ago
  • Fugl-Meyer Upper Extremity score between 20 and 56 out of 60
  • Inducible motor evoked potential of the abductor pollicis brevis on the affected side
  • Presence of unilateral neglect confirmed by Virtual Reality Lateralized Attention Test score below 18
Not Eligible

You will not qualify if you...

  • History of cortical hemorrhagic stroke
  • History of seizures
  • History of brain tumor
  • Presence of hardware in the skull or spine such as coils or clips
  • Having an implantable medical device like a pacemaker
  • Presence of metal in the body that is not compatible with MRI
  • Pregnancy
  • Severe spasticity with Modified Ashworth Scale score of 3
  • Severe aphasia or cognitive impairment affecting comprehension
  • Unable to travel to the Upper Extremity Motor Function Laboratory for study participation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA

Pittsburgh, Pennsylvania, United States, 15240

Actively Recruiting

Loading map...

Research Team

E

Emily S Grattan, PhD MS BS

CONTACT

G

George F Wittenberg, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

OTHER

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here