ptake and effectiveness of a tailor-made online lifestyle advice for Dementia Risk Reductio
- Conditions
- dementia, Alzheimer's disease, Vascular dementia, prevention, risk reduction, lifestyledementie, de Ziekte van Alzheimer, vasculaire dementie, preventie, risico reductie, leefstijl
- Registration Number
- NL-OMON24336
- Lead Sponsor
- niversity Medical Center Groningen (UMCG)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 378
Inclusion Criteria
Middle-aged adults with a parent who is recently diagnosed with Alzheimer's disease or Vascular dementia.
- Age between 40 and 60 years
Exclusion Criteria
- Pregnant women or women were pregnant in the last 12 months
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is the uptake (e.g. the percentage of eligible people that signed the online informed consent form and completed baseline risk assessment). The total number of eligible people in each recruitment group (active versus passive) will be based on the number of new cases of AD or VD (dementia patients) in all memory clinics during the recruitment period, assuming an average of one child per dementia patient. Monthly, the number of eligible participants (e.g. new cases of AD and VD) will be monitored using the medical records of each memory clinic.
- Secondary Outcome Measures
Name Time Method