Spatial-Motor Stroke-Rehab Study
Emory University · with National Institute of Neurological Disorders and Stroke (NINDS) · NCT06053320
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–90 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 65
- US sites recruiting
- 3
- Study start
- April 11, 2023
- Record last updated
- May 20, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is 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.
Being studied: Prism adaptation therapy (PAT) + Electrical stimulation (E-stim); Prism adaptation therapy (PAT) + Sham Stimulator; Gait Training
Conditions: Spatial Neglect; Stroke
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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 the 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, and unexplained dizziness in the past 6 months
Individuals with right hemisphere stroke (40-90 years)
- History 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
- 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.
Recruiting US locations
Emory Rehabilitation Hospital
Atlanta, GA 30322
Site contact: Fisayo Aloba, PT, DPT · olufisayo.aloba@emory.edu
Emory University Hospital (EUH)
Atlanta, GA 30322
Site contact: Fisayo Aloba, PT, DPT · olufisayo.aloba@emory.edu
Executive Park
Atlanta, GA 30329
Site contact: Fisayo Aloba, PT, DPT · olufisayo.aloba@emory.edu
Study contacts (from the official record)
- Fisayo Aloba, PT, DPT · 404-712-5803 · olufisayo.aloba@emory.edu
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