Electrical spinal stimulation with arm training for stroke arm weakness
Tests spinal electrical stimulation with arm training in adults with stroke-related arm weakness.
Plain-language title generated from the registry record
Registry title: Transcutaneous Electrical Stimulation for Stroke Patients
Key facts
- Where
- Chicago, United StatesSee the site
Where in United States
- Shirley Ryan AbilityLabChicago, United StatesTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Shirley Ryan AbilityLab
- Trial code
- NCT06950593
- Record updated
- 12 August 2025
- Original description
This study aims to evaluate the feasibility and impact of transcutaneous electrical stimulation of the spinal cord (TESS) on the recovery of post-stroke individuals who have upper limb hemiparesis. It will compare outcomes measures between individuals who receive upper limb task specific training with TESS and individuals who receive task specific training of the upper limb with Sham, or fake, TESS.Read full original descriptionShow less
Upper Limb Function Following Transcutaneous Electrical Spinal Cord Stimulation in Individuals With Hemiplegic Stroke
This study aims to evaluate the feasibility and impact of transcutaneous electrical stimulation of the spinal cord (TESS) on the recovery of post-stroke individuals who have upper limb hemiparesis. It will compare outcomes measures between individuals who receive upper limb task specific training with TESS and individuals who receive task specific training of the upper limb with Sham, or fake, TESS.
Inclusion: 18 years or older; able and willing to give written consent and comply with study procedures; at least 6 months post-stroke; hemiplegia secondary to stroke; UE Fugle Meyer Assessment <35; not currently receiving regular occupational therapy services; participant has received clearance from physician to participate in study; participant has at least a rudimentary comprehension of English.
Exclusion: orthopedic dysfunction, injury, or surgery that would impact the individual's ability to use the upper extremities; using a powered, implanted cardiac device for monitoring or support of heart function (i.e. pacemaker, defibrillator, or LVAD), or anti-spasticity implantable pumps, or cochlear implants; active cancer or cancer remission less than 5 years; traumatic brain injury or neurological conditions that would impact the study; botox injection in upper extremity within the last 4 months; modified ashworth score of 4 in any joint of the affected limb; pregnant or nursing; unhealed bone fractures; severe contractures in the upper extremities; recent procedure or operation of the spinal cord within the past year; skull fracture that has developed within the past 6 months; non-English speakers.