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Tailored Education for Aging and Cognitive Health: A Health Behavior Change Intervention for Midlife Adults at Risk for Alzheimer's Disease and Related Dementias

Key facts

Who runs it
Rhode Island Hospital
Where
Providence, United StatesSee the site
Trial code
Status
Not yet recruiting
People taking part
280 people, planned
Starts
15 Feb 2027
Expected to end
30 Sept 2031
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • TEACH
  • Basic health education
Record updated
12 November 2026

Who can take part

Age
40 years to 69 years
Sex
Women and men
Healthy volunteers
Can take part

The registry criteria, word for word

Show all 12 criteriaShow less

Who can take part

  • Age 40-69 years
  • Normal cognition (Telephone Interview for Cognitive Status-Modified > 32)
  • English language fluency
  • Participants must have at least two of six dementia risk factors:; BMI in the overweight or obesity range ( >24.9); Systolic blood pressure in the "elevated" range or higher (>120 mmHg); LDL cholesterol outside the "optimal" range (>100 mg/dL); HbA1C in the prediabetes or diabetes range (> 5.6%); APOE e4 allele; First-degree relative with ADRD
  • Participants must have suboptimal engagement in at least one core health behavior:; Diet: Mediterranean Diet Adherence Screener (MEDAS) total score < 10; Physical activity: <120 minutes of moderate-intensity or <60 minutes of vigorous-intensity physical activity per week; Sleep: <=7 hours of sleep per night (past-week average)

Who cannot take part

  • Prior diagnosis of Mild or Major Neurocognitive Disorder
  • History of serious mental illness (i.e., schizophrenia, bipolar disorder)
  • History of neurodevelopmental disorder (e.g., intellectual disability)
  • Severe physical disability or unstable medical conditions that prevent safe engagement in recommended study activities (e.g., physical activity)
  • Current alcohol or substance use disorder based on self-report
  • Current Beck Depression Inventory score > 28
  • Current enrollment in an ADRD prevention clinical trial

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 69 years old?

Where in United States

  • Rhode Island HospitalProvidence, United StatesContact: Laura Korthauer, Ph.D.No longer taking part

About the trial

What the trial wants to find out

This Stage II behavioral intervention development project will examine the efficacy of a multi-domain health behavior intervention for primary prevention of Alzheimer's disease and related dementias (ADRD) in middle age.

The 2 groups in the trial

  • ExperimentalTreatment being tested

    TEACH Intervention

    Treatment: TEACH

  • ControlExisting treatment, for comparison

    Basic Health Education

    Treatment: Basic health education

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Testing the Efficacy of a Personalized Multi-Domain Behavioral Intervention for Alzheimer's Disease and Related Dementias Risk Reduction in Midlife
Fit questions
Built from NCT07933367, who can take part
Record updated
12 November 2026