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

Launched by UNIVERSITY HEALTH NETWORK, TORONTO · May 15, 2025

Trial Information

Current as of July 21, 2025

Recruiting

Keywords

Functional Electrical Stimulation Transcutaneous Spinal Cord Stimulation Postural Control

ClinConnect Summary

The SPARC trial is a research study looking into ways to help people who have had a stroke improve their balance and reduce the risk of falling. After a stroke, many individuals become more mobile, but unfortunately, this also increases their chances of falling. The study is exploring whether using electrical stimulation combined with balance training can help with this problem. The main goal is to see if enough people are interested in joining a larger study and if they are comfortable with the procedures involved.

To be eligible for this trial, participants need to be at least 18 years old and have had a specific type of stroke more than a year ago. They should be living at home and able to stand independently for at least 60 seconds. Participants will not be accepted if they have other conditions that affect balance or certain medical issues that could interfere with the study's procedures. Those who join can expect to engage in exercises and receive electrical stimulation to help improve their balance, with the hope that this will lead to better recovery and fewer falls after a stroke.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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 Criteria:
  • Any condition other than stroke that significantly affects their postural control (e.g. vestibular disorder, vision loss)
  • A prior lower extremity fragility fracture
  • A planned injection of botulinum toxin to the legs during the intervention period
  • Peripheral nerve damage in the legs
  • Contraindications for FES (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)
  • Previous participation in FES or tSCS within the past 2 years (May affect blinding integrity. Likely uncommon; FES is rarely used in Canada post-stroke.)

About University Health Network, Toronto

University Health Network (UHN), based in Toronto, is a leading academic health sciences center dedicated to advancing patient care through innovative research and education. As a prominent sponsor of clinical trials, UHN integrates cutting-edge scientific discoveries with clinical practice, facilitating the development of new therapies and treatment modalities. With a commitment to improving health outcomes, UHN collaborates with a diverse network of researchers, healthcare professionals, and industry partners, fostering an environment that prioritizes patient safety and ethical standards in clinical research. Through its extensive resources and expertise, UHN plays a pivotal role in transforming healthcare and enhancing the quality of life for patients both locally and globally.

Locations

Toronto, Ontario, Canada

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported