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Spatial-Motor Stroke-Rehab Study

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Emory University

Status

Enrolling

Conditions

Spatial Neglect
Stroke

Treatments

Device: Prism adaptation therapy (PAT) + Sham Stimulator
Device: Prism adaptation therapy (PAT) + Electrical stimulation (E-stim)
Other: Gait Training

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06053320
STUDY00005012
1F31NS131020-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to understand how prism adaptation training with and without electrical stimulation changes visuospatial behavior, motor system neurophysiology, and walking dysfunction.

Full description

Spatial Neglect (SN) is defined as pathological asymmetric spatial behavior causing functional disability and occurs in greater than 50% of individuals with right hemisphere stroke. SN post-stroke is associated with increased fall risk, increased hospital length of stay, poorer rehabilitation outcomes, and severe long-term disability. Prism adaptation therapy (PAT) is an evidence-based treatment for SN after stroke, however, the effects of SN on gait are not well known. Neuromuscular electrical stimulation delivered via surface electrodes is a common therapeutic adjunct in stroke rehabilitation, including for SN and gait training. However, the additive therapeutic effects of combining electrical stimulation and PAT, as well as the effects of motor training on gait deficits associated with SN are poorly understood. Furthermore, although there is limited literature examining the effects of electrical stimulation on corticospinal tract output (CST), there is an inadequate understanding of the neural mechanisms of PAT and the combinatorial effects of PAT with electrical stimulation. To parse out the neural mechanisms of PAT and electrical stimulation on the visuospatial system, researchers will first examine the effects of PAT with or without electrical stimulation in neurologically unimpaired adults, researchers will then compare results to individuals with stroke with spatial neglect.

The primary objective is to study the effects of PAT on visuospatial behavior and motor cortical excitability in able-bodied individuals (young and older), and on spatial neglect, motor cortical neurophysiology, and walking function in individuals post-stroke.

The long-term goal of this project is to develop novel, effective, and personalized rehabilitation protocols targeting SN deficits and gait dysfunction to reduce disability in stroke survivors. The rationale of this project is to explore and generate data regarding future novel combinatorial motor-spatial retraining approaches that will enhance the rehabilitation approach of SN and gait performance in individuals post-stroke.

Enrollment

65 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Young Adults Able Bodied (YAB) Individuals

  • 18-30 years
  • Able-Bodied (healthy without any physical disability or neurological disorder)

Older Adults Able-Bodied Individuals (OAB)

  • 45-90 years
  • Able-Bodied (healthy without any physical disability or neurological disorder)

Individuals with right hemisphere stroke (40-90 years)

  • >3 months following stroke.
  • Presence of Aiming SN
  • Ability to walk >10m with or without assistive devices.
  • Unilateral left-sided hemiparesis with gross arm strength of ≤ grade 4/5 on the Medical Research Council Scale
  • Ability to follow 3-stage commands and provide informed consent.

Exclusion criteria

Young Adults Able Bodied (YAB) Individuals and Older Adults Able-Bodied Individuals (OAB)

  • History or evidence of orthopedic or physical disability
  • History or evidence of neurological pathology
  • Pregnancy (female)
  • Uncontrolled hypertension
  • Cardiac pacemaker or other implanted electronic system
  • Presence of skin conditions preventing electrical stimulation setup
  • Impaired sensation in the left upper limb.
  • Bruises or cuts at the stimulation electrode placement site
  • Concurrent enrollment in rehabilitation or another investigational study.
  • History or evidence of orthopedic or physical disability interfering with study procedures
  • History or evidence of neurological pathology or disorder
  • Severe uncontrolled medical problems (e.g., hypertension, cardiovascular disease, rheumatoid arthritis, active cancer or renal disease, epilepsy) that may interfere with study procedures
  • Contraindications to TMS such as metal implants, medications that can increase cortical excitability, unexplained dizziness in the past 6 months

Individuals with right hemisphere stroke (40-90 years)

  • History of multiple strokes or brainstem strokes
  • Cerebellar disorders
  • Impaired sensation in the left upper limb.
  • History of other neurological disorders
  • Uncontrolled hypertension
  • Cardiac pacemaker or other implanted electronic system
  • Pregnancy (female)
  • Presence of skin condition
  • Bruises at the electrode placement site
  • Concurrent enrollment in rehabilitation or another investigational study
  • Severe uncontrolled medical problems (e.g., hypertension, cardiovascular disease, rheumatoid arthritis, active cancer or renal disease, epilepsy) or other medical conditions that can interfere with study procedures
  • Contraindications to TMS such as metal implants in the brain, medications that will increase cortical excitability, etc.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

65 participants in 3 patient groups

Young Able-Bodied individuals
Active Comparator group
Description:
18-30 years old able-bodied individuals (healthy without any physical disability or neurological disorder).
Treatment:
Device: Prism adaptation therapy (PAT) + Electrical stimulation (E-stim)
Device: Prism adaptation therapy (PAT) + Sham Stimulator
Old Able-Bodied individuals
Active Comparator group
Description:
45-90 years old able-bodied individuals (healthy without any physical disability or neurological disorder).
Treatment:
Device: Prism adaptation therapy (PAT) + Electrical stimulation (E-stim)
Device: Prism adaptation therapy (PAT) + Sham Stimulator
Stroke with Spatial Neglect (SN) individuals
Experimental group
Description:
40-90 years individuals with more than 3 months following right hemisphere stroke.
Treatment:
Other: Gait Training
Device: Prism adaptation therapy (PAT) + Electrical stimulation (E-stim)
Device: Prism adaptation therapy (PAT) + Sham Stimulator

Trial contacts and locations

3

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Central trial contact

Fisayo Aloba, PT, DPT

Data sourced from clinicaltrials.gov

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