Kimel Family Centre for Brain Health and Wellness (NCT06933667)
🩺 Plain-English Summary (8th-Grade Level)
Participants (n=450; aged 50+; without a diagnosis of dementia; sufficiently fluent in English to complete the assessments and engage in programming) receive a comprehensive dementia risk assessment, including nonmodifiable and modifiable risk factors, from which they receive a Personalized Dementia Risk Report and Program Strategy, indicating their health conditions increasing and their risk level in five modifiable risk domains: physical activity, brain- healthy eating, cognitive engagement, social connections, and mental wellbeing. Equipped with this information, participants enroll in programs within the Centre to address their risk factors. Changes to their dementia risk, cognition, and Personalized Program Strategy are communicated through re-assessments of risk factors every six months (risk and cognition) and every year (comprehensive assessment).
Who can join: Review the eligibility criteria below.
Location: Baycrest — Toronto, Ontario
Age range: 50 Years
🧪 Interventions in This Study
- Physical Activity (BEHAVIORAL)
- Brain-healthy Eating (BEHAVIORAL)
- Cognitive Engagement (BEHAVIORAL)
- Social Connections (BEHAVIORAL)
- Mental Wellbeing (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Baycrest — Toronto, Ontario
📞 Contact the Study Coordinator
Phone: (416) 785-2500
Email: nanderson@research.baycrest.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 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 § 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.
More studies in Prevention
- Apple Heart & Movement Study — Boston, Massachusetts
- Developing Biomarker-Supported Schizophrenia Spectrum Disorder (SSD) Prevention — Houston, Texas
- Enhancing an Existing Prevention Strategy to Reduce Intentional Firearm Injuries Among High-risk Youth (Phase 1) — Richmond, Virginia
- Optimizing PrEP Uptake and Adherence Among Male Sex Workers — Los Angeles, California
- A Randomized Controlled Trial Testing the Effect of the Youth Mindful Awareness Program on Negative Affect (YMAP2). — Los Angeles, California
Explore by condition: All Prevention clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.