Tailored Education for Aging and Cognitive Health: A Health Behavior Change Intervention for Midlife Adults at Risk for Alzheimer's Disease and Related Dementias
A legfontosabb adatok
- Hol
- Providence (Egyesült Államok)A helyszín megnézése
Neked szólhat?
Magadról válaszolj. Ez nem döntés: hogy részt vehetsz-e, azt csak a vizsgálat csapata mondhatja meg.
- 40 és 69 év között vagy?
Forrás: NCT07933367: ki vehet részt
Helyszínek itt: Egyesült Államok
- Rhode Island HospitalProvidence, Egyesült ÁllamokContact: Laura Korthauer, Ph.D.No longer taking part
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Rhode Island Hospital
- Azonosító
- NCT07933367
- A regiszteradat frissítve
- 2026. november 12.
- Eredeti leírás
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.A teljes eredeti leírásKevesebb
Testing the Efficacy of a Personalized Multi-Domain Behavioral Intervention for Alzheimer's Disease and Related Dementias Risk Reduction in Midlife
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.
Bevonási feltételek: 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).
Kizáró feltételek: 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.