πŸ›οΈ Verified NIH Record β€’ Updated 2026-07-02

Protecting the Brain From Post-Stroke Cognitive Impairment and Dementia With Multimodal Exercise Training (NCT07445841)

Protecting the Brain From Post-Stroke Cognitive Impairment and Dementia With Multimodal Exercise Training: A Bayesian Adaptive Trial (PROTECT)

🟒 Recruiting Observational / Diagnostic πŸ“‹ Clinical Research Protocol Sponsor: McGill University

🩺 Plain-English Summary (8th-Grade Level)

The rates of cognitive decline and dementia after stroke are disproportionately high. Strategies that can protect the brain early after the stroke event could reduce the future risk of cognitive decline and dementia in these patients. Although physical exercise is usually recommended after stroke, there is very little information about the protective effect of exercise implemented in early stages of recovery as a potential protective measure against cognitive decline and dementia risk in these patients. This study will investigate the effect of a multimodal exercise intervention implemented early after the stroke event on cognition and on a selected group of markers that can predict cognitive decline and dementia risk.

Who can join: Review the eligibility criteria below.

Location: McMaster University β€” Hamilton, Ontario

Age range: 40 Years to 80 Years

πŸ§ͺ Interventions in This Study

  • Multimodal Training (OTHER)
  • Balance, Toning and Stretching (OTHER)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (2 Sites)

  • McMaster University β€” Hamilton, Ontario
  • Jewish Rehabilitation Hospital β€” Laval, Quebec

πŸ“ž Contact the Study Coordinator

Phone: (514) 398-4400

Email: marc.roigpull@mcgill.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Stroke clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—