Authors
Christina Soong, Daniel D Veith, Megan L Gill, Lisa A Beck, Julie B Block, Anders J Asp, K A Fernandez, Margaux B Linde, Candee J Mills, Tyson L Scrabeck, Omid Jahanian, Peter J Grahn, Kristin D Zhao, Ryan Solinsky
Published in
The journal of spinal cord medicine. Pages 1-12. Aug 20, 2026. Epub Aug 20, 2026.
Abstract
This study aimed to evaluate the off-target effects of motor-optimized SCS-enabled task-specific training (SCS-TST) on lower urinary tract function through self-reported data from individuals with chronic spinal cord injury (SCI), using the Neurogenic Bladder Symptom Score (NBSS). A secondary objective was to explore whether participant characteristics or bladder treatments were associated with changes in NBSS outcomes.
Datasets from two prospective pilot trials using percutaneous spinal cord stimulation (SCS) to enable motor function were analyzed and reported.
Department of Physical Medicine and Rehabilitation, Mayo Clinic, Rochester, Minnesota.
Adults ≥ 1-year post traumatic SCI.
Participants received either 12 days of epidural stimulation (ES) or 10 days of ES and dorsal root ganglion stimulation (ESDRS), each coupled with 6-8 SCS-TST sessions.
NBSS was administered pre- and post-intervention.
Analysis of 23 participants (ES, n = 3; ESDRS, n = 20) showed no significant group-level changes in total NBSS (p = 0.49) or functional domains (p = 0.56-0.85). Individually, 83% demonstrated no clinically meaningful change, while 9% improved and 9% worsened. Exploratory analyses identified that symptom change was associated with neurological level of injury (p = 0.017), age (p = 0.026), and marginally associated with injury severity (p = 0.055). Oxybutynin use was associated with lower symptom variability, without statistical significance (p = 0.074).
Motor-optimized SCS-TST did not lead to significant group-level changes in patient-reported urinary symptoms. However, a subset of individuals experienced improvement or worsening, suggesting that injury characteristics and medication use may influence urinary outcomes. These preliminary findings warrant confirmation in larger, adequately powered trials.Trial Registration: ClinicalTrials.gov identifiers: NCT05095454, NCT04736849.
PMID:
42622482
Bibliographic data and abstract were imported from PubMed on 20 Aug 2026.
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