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

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
United States
Illinois
Shirley Ryan AbilityLab
RECRUITING
Chicago
Contact Information
Primary
Mary Ellen Stoykov, PhD, OT
mstoykov@sralab.org
773-704-2422
Time Frame
Start Date: 2025-08-18
Estimated Completion Date: 2027-01-01
Participants
Target number of participants: 14
Treatments
Active_comparator: Experimental Group
This group receives task specific training and transcutaneous spinal cord stimulation (TESS) during treatment sessions. TESS is applied via electrodes placed vertically over the spinous processes of C5-C6. The stimulation will be adjusted within a range of 10mA to 100mA based on participant tolerance and will be delivered for 30 minutes per training session.
Active_comparator: Comparator Group
This group receives task specific training without real TESS during treatment sessions. Instead, they receive Sham TESS, which is a placebo version in which the electrodes are applied and the stimulation is turned on so that the patient can feel it, and then ramped down to zero for the duration of the session.
Related Therapeutic Areas
Sponsors
Leads: Shirley Ryan AbilityLab

This content was sourced from clinicaltrials.gov

Similar Clinical Trials