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Stimulating Postural Control to Augment Rehabilitation After Cerebral Stroke (SPARC): a Pilot Trial

Key facts

Where
Toronto, CanadaSee the site

Where in Canada

  • KITE Research Institute, Toronto Rehabilitation Institute - University Health NetworkToronto, CanadaTaking people

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  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University Health Network, Toronto
Trial code
NCT06987682
Record updated
23 March 2026
Original description
People living with stroke have a high risk of falling and this risk increases as mobility improves over the first year post-stroke. Despite the high number of falls, there is a lack of interventions to prevent falls after stroke. One possible solution is to alter nerve activity through delivery of a stimulus, such as electrical stimulation. The purpose of this study is to describe and compare clinical, biomechanical and nerve-related outcomes between individuals with stroke who receive RBT with tSCS and those who receive RBT with sham tSCS.Read full original descriptionShow less

People living with stroke have a high risk of falling and this risk increases as mobility improves over the first year post-stroke. Despite the high number of falls, there is a lack of interventions to prevent falls after stroke. One possible solution is to alter nerve activity through delivery of a stimulus, such as electrical stimulation. The purpose of this study is to describe and compare clinical, biomechanical and nerve-related outcomes between individuals with stroke who receive RBT with tSCS and those who receive RBT with sham tSCS.

Inclusion: Aged 18 years or greater; Diagnosed with a middle cerebral artery stroke >1 year ago; Community-dwelling (i.e. not living in long-term care or other inpatient setting); Able to stand independently for 60 seconds; Able to understand spoken English.

Exclusion: A prior lower extremity fragility fracture; Previous participation in tSCS within the past 2 years (May affect blinding integrity. Likely uncommon; FES is rarely used in Canada post-stroke.); Any condition other than stroke that significantly affects their postural control (e.g. vestibular disorder, vision loss); Contraindications for electrical stimulation (i.e. implanted electronic device, active cancer or radiation in past six months, uncontrolled epilepsy, skin rash/wound at an electrode site, pregnancy, active deep vein thrombosis); Contraindications for TMS (i.e. seizures, metal in the head); A planned injection of botulinum toxin to the legs during the intervention period; Peripheral nerve damage in the legs.

ClinicalTrials.gov NCT06987682