Clinical Research Directory

Inclusion Criteria: * 60-79 years of age at pre-screening; * Adequate fluency in Dutch to understand the informed consent and complete questionnaires; * Providing informed consent to all study procedures; * Internet access at home; * Presence of ≥3 self-reported risk factors for cognitive decline (must contain at least 2 modifiable risk factors and 1 non-modifiable riskfactor). Exclusion Criteria: * Diagnosis of dementia or mild cognitive impairment at baseline (self-reported); * Significant cognitive impairment assessed using the Modified Telephone Interview for Cognitive Status battery (TICSm score\<23); * Conditions affecting safe and continuous engagement in the intervention (e.g. under treatment for current malignant diseases, major psychiatric disorders (e.g. major depression, psychosis, bipolar disorder), neurological disorders (e.g. Parkinson's disease, multiple sclerosis), symptomatic cardiovascular disease (e.g. stroke, angina pectoris, heart failure, myocardial infarction), re-vascularization within three months, severe loss of vision, hearing or communicative ability, severe mobility impairment, other conditions preventing co-operation) as judged by the local study nurse or consulted physician at the local study site; * Coincident participation in any other intervention trial at time of pre-screening. * Coincident participation of spouse in FINGER-NL trial.