A Closed Loop Neural Activity Triggered Stroke Rehabilitation Device
University of Wisconsin, Madison · with American Heart Association · NCT02098265
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+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 288
- US sites recruiting
- 1
- Study start
- June 2010
- Record last updated
- September 17, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this research is to determine if two non-invasive brain stimulation techniques, muscle stimulation of the arm and neuro-stimulation through the tongue, can increase the extent of stroke recovery.
Being studied: Functional Electric Stimulation (FES); Behavioral Assessments; Magnetic Resonance Imaging; EEG; RecoveriX; Delay; BCI-FES
Conditions: Stroke
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria (Experimental Group):
- Stroke patients with persistent upper extremity (UE) deficits
Inclusion Criteria (Control Group 1)
- Stroke patients without UE impairments
- Participants with risk factors for stroke
- healthy controls
- No known neurologic, psychiatric or developmental disability
Inclusion Criteria (Control Group 2)
- Stroke patients with persistent upper extremity (UE) deficits
- Moderate upper extremity (dominant right hand affected) impairment (score of 1 or 2 on the motor sub-component of the NIH stroke scale (NIHSS) and ARAT score 20-45)
- No upper extremity injury or conditions that limited use prior to the stroke
- Pre-stroke independence with a Modified Rankin Score of 0 or 1, for the standard FES only intervention.
Exclusion Criteria (for all participants):
- Allergic to electrode gel, surgical tape and metals
- Participants under treatment for infectious diseases or having apparent oral lesions or inflammation will be excluded from the study
- Women who are pregnant or may become pregnant during the course of the study will be excluded
- Participants with contraindications for MRI will be offered the opportunity to participate in the interventions study only (e.g. EEG-BCI-FES and behavioral testing)
Exclusion Criteria (for healthy controls)
- Contraindications for MRI
- Allergic to electrode gel, surgical tape, and metals.
Recruiting US locations
University of Wisconsin
Madison, WI 53706
Site contact: Veena Nair, PhD · 608-265-5269 · vnair@uwhealth.org
Study contacts (from the official record)
- Radiology Studies · 608-282-8349 · Radstudy@uwhealth.org
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