NCT07831616 · NOT YET RECRUITING
Development and Empirical Evaluation of a Brief Lifestyle Intervention for Older Adults at Risk of Dementia Within an Integrated Medical-Preventive Grid-Based Service Model
This study develops and tests a brief lifestyle intervention, delivered by physicians at community health clinics, for older adults (60+) at elevated dementia risk based on a risk-scoring tool. It's a non-drug, real-world feasibility study, not a phase-numbered drug trial, so it's an early look at whether this approach works in everyday primary care settings.
You may qualify if
- Age ≥ 60 years
- CAIDE dementia risk score ≥ 6
- Possessing basic comprehension and verbal expression abilities
- Voluntarily participating in the study and signing the informed consent form
- Not participating in other clinical trials during the intervention period.
You're excluded if
- Individuals already diagnosed with dementia
- individuals with severe heart, liver, or kidney disease
- individuals with severe chronic diseases and comorbidities (e.g., congestive heart failure, or hypertension or diabetes with severe complications)
- individuals with severe visual or hearing impairment.
The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.
Eligibility criteria as of 2026-09-21