BridgeMD
New treatment option for Upper Limb Hemiparesis Following Stroke
Official title Transcutaneous Electrical Stimulation for Stroke Patients
ClinicalTrials.gov ID: NCT06950593
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- 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
You likely can't join if
- 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
- using a powered, implanted cardiac device for monitoring or support of heart function (i.e. pacemaker, defibrillator, or LVAD), or anti-spasticity...
- unhealed bone fractures
- severe contractures in the upper extremities
See the full eligibility criteria
- 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
- 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
- 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
- unhealed bone fractures
- severe contractures in the upper extremities
- active cancer or cancer remission less than 5 years
- orthopedic dysfunction, injury, or surgery that would impact the individual's ability to use the upper extremities
- recent procedure or operation of the spinal cord within the past year
- traumatic brain injury or neurological conditions that would impact the study
- skull fracture that has developed within the past 6 months
- non-English speakers
The study team makes the final eligibility decision.
Where it's taking place
- Chicago, Illinois, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Chicago, Illinois, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.