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NCT07153536Recruiting

Spinal Cord Stimulation Combined With Physical Therapy in Post-Stroke Upper-Limb Motor Hemiparesis

Source: ClinicalTrials.gov · Last updated 22 Jun 2026

Brief summary (registry, in English)

This study plans to use systems that have been developed by Medtronic to investigate the use of cervical spinal cord stimulation to treat adults with upper limb hemiparesis resulting from a stroke. The spinal cord stimulation (SCS) will be combined with physical training to improve arm and hand motor control. The study is divided into three phases. In the first phase, after baseline assessments, participants will undergo a Physical Training Protocol (PTP) for 6 weeks including 3 sessions of 90 mins/session per week. After receiving the Medtronic implantable system, in Phase 2, they will then repeat the same PTP program in combination with spinal cord stimulation during the entirety of each of the rehabilitation sessions. Finally, in Phase 3, participants will go home, will not be able to use the stimulation at home but will participate in monthly assessments in the laboratory in which the functionality of the Medtronic system and their motor performances will be assessed for up to 6 months.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
20 Aug 2025
Start date
6 Jan 2026
Primary completion date
31 Aug 2027
Lead sponsor
Marco Capogrosso
Diseases
Stroke
NCT number
NCT07153536

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 6 Jan 2026 to the primary completion date, 31 Aug 2027
  • 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

  • Participants that cannot suspend their antiplatelets and/or anticoagulant therapy for two weeks around the time of surgery
  • Obstructed or restricted epidural spinal canal to the point of hindering or increasing the risk of implant of the spinal leads as judged by the study surgeon upon screening imaging
  • Taking anti-spasticity or anti-epileptic medications
  • T-score higher than 63 on the 18-question Brief Symptoms Inventory (BSI-18) who have undergone discussions with and been deemed unsuitable by the Principal Investigator and a study physician
    • Potential participants who may be excluded on initial screening may discuss possible medication changes with their physician.

Other illness

  • Presence of any serious disease or disorder (ex. Neurological conditions other than stroke, cancer, severe cardiac or respiratory disease, renal failure, etc.) that could affect their ability to participate in this study
  • Considered to be at high-risk of recurrent stroke as evident from their medical history or upon judgment of the study physician
  • Presence of post-stroke central pain, other forms of pain or other constraints such as joint contractures in the paretic arm that are serious enough to prevent or affect the correct execution of the physical training protocol as judged by the study therapist

Age

  • Female participants of child-bearing age who are pregnant or breastfeeding during the study

Other

  • A score on the Short Blessed Test assessment scale lower than 9
  • Existence of any implanted medical device that is not MRI safe and/or any active medical devices even if it is MRI safe
  • Implanted spinal fusion and stabilization devices such as plates and rods between the C2 and T3 spinal vertebra
  • Severe claustrophobia that prevents execution of the required MRI imaging sessions

Who the study is looking for

  • Experienced an ischemic or hemorrhagic stroke that resulted in arm and hand hemiparesis more than 6 months prior to the time of enrollment (Prior strokes that did not cause upper extremity motor deficits are not exclusionary.)
  • Age 22 to 70 years old
  • Upper extremity motor score higher than 20 and lower than or equal to 45 on the Fugl-Meyer Assessment (FMA) scale
  • FMA upper extremity sensory score higher than 6 points (out of 12 points)
  • The ability to communicate, understand, give appropriate consent and follow two-step commands

Age in the registry: 22 years to 70 years · 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
University of Pittsburgh
Coordinator of this site? Confirm its status
PittsburghUnited StatesRecruiting

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