Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06987682

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

Led by University Health Network, Toronto · Updated on 2026-03-23

16

Participants Needed

1

Research Sites

132 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or greater
  • Diagnosed with a middle cerebral artery stroke more than 1 year ago
  • Living in the community (not in long-term care or inpatient setting)
  • Able to stand independently for 60 seconds
  • Able to understand spoken English
Not Eligible

You will not qualify if you...

  • Any condition other than stroke that significantly affects postural control (e.g., vestibular disorder, vision loss)
  • Prior lower extremity fragility fracture
  • Planned injection of botulinum toxin to the legs during the intervention period
  • Peripheral nerve damage in the legs
  • Contraindications for electrical stimulation (implanted electronic device, active cancer or radiation in past six months, uncontrolled epilepsy, skin rash or wound at electrode site, pregnancy, active deep vein thrombosis)
  • Contraindications for transcranial magnetic stimulation (seizures, metal in the head)
  • Previous participation in transcutaneous spinal cord stimulation within past 2 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

KITE Research Institute, Toronto Rehabilitation Institute - University Health Network

Toronto, Ontario, Canada, M4G 3V9

Actively Recruiting

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Research Team

K

Kristin E Musselman, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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