Brain Health PRO online program to reduce dementia risk
Official title: The Brain Health PRO Online Risk Factor Reduction Study for The Canadian Therapeutic Platform Trial for Multidomain Interventions to Prevent Dementia
Run by University of British Columbia · NCT07364019 · Data updated 2026-11-12
This online program tests whether a six‑month lifestyle education plan can help people aged 50–80 who are at risk for dementia reduce their risk factors.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 50 Years to 80 Years |
| Sex | All |
| Enrollment | 700 (estimated) |
| Sponsor | University of British Columbia Academic / other |
| Locations | 1 site (Vancouver, British Columbia) |
| Status | Recruiting |
| Started | May 7, 2026 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | May 19, 2026 |
| Trial ID | NCT07364019 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 50–80 with at least one dementia risk factor (e.g., family history, lower education, hypertension, high cholesterol, BMI > 30) who can participate in online assessments and education in English or French.
✕Probably not a fit
Individuals without access to reliable internet or who are not at increased dementia risk may derive little or no benefit from this program.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Adults 50–80 at increased dementia risk are randomly assigned to start the Brain Health PRO program immediately or after six months. The intervention uses online education about evidence-based lifestyle changes to lower dementia risk factors and engage participants in brain health actions. All participants have access to the material for 12 months following initial access, and assessments are conducted remotely. The trial aims to see if online education can be practically implemented across a diverse Canadian population to support dementia prevention. Results will inform whether scalable digital lifestyle interventions can contribute to reducing dementia risk.
Why it matters
Potential benefit: If successful, participants may improve modifiable risk factors and gain sustained access to brain health resources that could lower their dementia risk.
How similar studies have gone: Digital, education-based lifestyle interventions have shown promise in reducing risk factors in similar populations, though large-scale evidence specific to online dementia risk reduction is still evolving.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Completion and documentation of the electronic Informed Consent Process (from the participant) * Sufficient proficiency in English or French to undergo online assessments and participate in an online educational program. * Technical ability to participate in an online educational program and remote assessments (i.e., regularly have access to a computer or tablet with an internet connection; have access to a desktop or laptop computer with an internet connection at least once every 6 months; ability to send and receive emails; ability to complete online assessments) * Sufficient vision to participate in an online educational program and complete online cognitive testing * Ages 50-80 * Classified as being at increased risk of dementia based on at least one of the following: * First-degree family history of dementia * Education level at or below high school (grade 12 or less) * Self-Reported: Hypertension, Hypercholesterolemia, Body Mass Index \> 30 kg/m2 (derived from NIH Metric BMI Calculator), or Physical Inactivity (active is defined as engaging in a minimum of 20- 30 min of physical activity causing sweating and breathlessness, at least 2 times a week) Exclusion Criteria: * Individuals who have a clinical diagnosis of Dementia (based on self-report) * Individuals who are currently participating in or have participated in a past study involving BHPro
Where it's running
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University of British Colubmia
Vancouver, British Columbia, Canada Recruiting
Study contacts
- Study coordinator: Pennny Slack, MSc
- Email: penny.slack@ubc.ca
- Phone: 604-822-6379
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.