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NCT06950593Recruiting

Transcutaneous Electrical Stimulation for Stroke Patients

Upper Limb Function Following Transcutaneous Electrical Spinal Cord Stimulation in Individuals With Hemiplegic Stroke

Source: ClinicalTrials.gov · Last updated 12 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
14 (estimated)
First submitted
20 Mar 2025
Start date
18 Aug 2025
Primary completion date
1 Jun 2026
Lead sponsor
Shirley Ryan AbilityLab
Diseases
Stroke
NCT number
NCT06950593

What you commit to

  • Study type: Interventional
  • Planned participants: 14
  • From 18 Aug 2025 to the primary completion date, 1 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • orthopedic dysfunction, injury, or surgery that would impact the individual's ability to use the upper extremities

Other illness

  • 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

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Shirley Ryan AbilityLab
Coordinator of this site? Confirm its status
ChicagoUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.