๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2024-10-25

SYNERGIC-2 Trial (SYNchronizing, Exercises and Remedies to GaIn Cognition@home) (NCT05375513)

A Home-based Personalized Multidomain RCT from the Canadian Therapeutic Platform for Multidomain Interventions to Prevent Dementia (CAN-THUMBS UP)

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿ“‹ Clinical Research Protocol Sponsor: London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

In Canada, 1,700,000 adults are at risk of dementia, half of them with MCI,representing one of the largest groups at risk for an incurable disease. Epidemiological evidence suggests up to 40% of dementia cases might be preventable by targeting modifiable lifestyle and cardiovascular factors. Given that current treatments cannot modify the disease, prevention is critical. SYNERGIC-2 offers a "personalized multidomain intervention" that combines physical and cognitive training, sleep, diet, and vascular-metabolic interventions in individuals with MCI to synergistically enhance their overall brain health including cognition and contributes to maintaining their independence. Importantly, interventions will be provided at home using an existing virtual platform reducing delivery complexity and expanding the accessibility to a wider population, thus decreasing potential inequities. Improving older adults' brain health and achieving even a modest two-year dementia incidence delay will have a projected saving of $218 Billion in Canada's healthcare system over 30 years.

Who can join: Review the eligibility criteria below.

Location: University of Alberta โ€” Edmonton, Alberta

Age range: 60 Years to 85 Years

๐Ÿงช Interventions in This Study

  • PMI@Home (OTHER)
  • Brain Health Pro (OTHER)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

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

๐Ÿ“ All Participating Trial Locations (8 Sites)

  • University of Alberta โ€” Edmonton, Alberta
  • University of British Columbia โ€” Vancouver, British Columbia
  • University of New Brunswick โ€” Fredericton, New Brunswick
  • St. Joseph's Health Care London, Parkwood Hospital โ€” London, Ontario
  • University of Ottawa โ€” Ottawa, Ontario
  • Baycrest Academy for Research and Education โ€” Toronto, Ontario
  • University of Waterloo โ€” Waterloo, Ontario
  • Concordia University โ€” Montreal, Quebec

๐Ÿ“ž Contact the Study Coordinator

Phone: (519) 646-6100

Email: Diana.Amaris@sjhc.london.on.ca

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

๐Ÿ’ฐ 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 ยง 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.

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—