NCT07698431 · RECRUITING

Personalized Brain Health Service and Dementia Prevention

This trial is testing whether a personalized Brain Health Service can help people with subjective cognitive decline — meaning they notice memory changes but score normally on tests — actually change their lifestyle habits and reduce their dementia risk. Participants get either a tailored 6-month program covering diet, exercise, sleep, and social engagement, or general prevention advice. This is a Phase NA feasibility study, meaning researchers are checking whether the approach is practical and acceptable before running a larger trial.

You may qualify if

  • Participants aged 55 to 85 with subjective cognitive complaints and normal screening test performance at the hospital.
  • Participants must have a minimal educational level for a neuropsychological assessment and a minimal digital literacy for the usage of smartphones, computers and Internet.

You're excluded if

  • Objective cognitive impairment.
  • Clinically relevant neurological disorders.
  • Major psychiatric disorders.
  • History of drug/alcohol abuse.
  • Unstable medical conditions that could fully explain cognitive complaints, as determined by the investigator.

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 2026-09-16

View full record on ClinicalTrials.gov

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