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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

NCT07933367, Not applicable, Not yet recruiting, Rhode Island Hospital

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleTailored Education for Aging and Cognitive Health: A Health Behavior Change Intervention for Midlife Adults at Risk for Alzheimer's Disease and Related DementiasClinicalTrials.gov
NCT numberNCT07933367ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment280 participants, estimatedClinicalTrials.gov
Lead sponsorRhode Island HospitalClinicalTrials.gov
ConditionsADRD, Alzheimer's Disease, Alzheimer's Disease and Alzheimer's Disease Related Dementias (AD/ADRD), Health Behavior, Healthy Aging, Vascular HealthClinicalTrials.gov
InterventionsTEACH, Basic health educationClinicalTrials.gov
First posted2026-11-12ClinicalTrials.gov
Last updated2026-11-12ClinicalTrials.gov

Registered outcomes 18

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryMultidomain behavioral compositebaseline, 2 months (end of treatment), 4 months, 12 months
This multidomain behavioral composite score is an unweighted average of five individual health behaviors: physical activity, Mediterranean diet adherence, cognitive activity, sleep quality, and alcohol use. Z-scores (or robust z-scores based on median/median absolute deviation for non-normal variables) for each continuous component score at baseline are calculated. Individual measures include 7-day average of moderate/vigorous physical activity measured via wearable (physical activity, total sleep time), Mediterranean Diet Adherence Tool total score (diet), Florida Cognitive Activities Scale (cognitive activity), and average units of alcohol consumed in the past two weeks (alcohol).
ClinicalTrials.gov
PrimaryMetabolic Syndrome Severity Score (MetS severity)baseline, 2 months (end of treatment), 4 months, 12 months
Race- and sex-specific weighted z-score based on confirmatory factor analysis from NHANES data (Gurka et al., 2012, 2014). MetS severity score is based on waist circumference, blood pressure, triglycerides, HDL cholesterol, and fasting plasma glucose
ClinicalTrials.gov
PrimaryDementia SomaSignal Testbaseline, 2 months (end of treatment), 12 monthsProteomic ADRD risk index that predicts 20-year risk of dementia from middle ageClinicalTrials.gov
SecondaryWearable measurement of moderate/vigorous physical activity minutesbaseline, 2 months (end of treatment), 4 months, 12 months7-day average of moderate to vigorous physical activity minutes, collected via wearableClinicalTrials.gov
SecondaryStep countbaseline, 2 months (end of treatment), 4 months, 12 months7-day average step count, collected via wearableClinicalTrials.gov
SecondaryTotal sleep timebaseline, 2 months (end of treatment), 4 months, 12 months7-day average total sleep time, collected via wearableClinicalTrials.gov
SecondaryMediterranean Diet Adherence Toolbaseline, 2 months (end of treatment), 4 months, 12 monthsstandardized assessment of adherence to the Mediterranean diet (self-report)ClinicalTrials.gov
SecondaryFlorida Cognitive Activities Scalebaseline, 2 months (end of treatment), 4 months, 12 monthsstandardized assessment of cognitive activities (self-report)ClinicalTrials.gov
SecondaryConsensus Sleep Diarybaseline, 2 months (end of treatment), 4 months, 12 monthsstandardized assessment of sleep quantity and quality (self-report)ClinicalTrials.gov
SecondaryInternational Physical Activities Scalebaseline, 2 months (end of treatment), 4 months, 12 months
standardized assessment of types and intensity of physical activity and sitting time that people do as part of their daily lives. This can be used to estimate total activity in MET-min/week and time spent sitting.
ClinicalTrials.gov
SecondaryPerceived Threat of ADRDbaseline, 2 months (end of treatment), 4 months, 12 monthsperceived threat and susceptibility of Alzheimer's disease and related dementias (7-item Likert scale)ClinicalTrials.gov
SecondaryDementia Awareness Questionnairebaseline, 2 months (end of treatment), 4 months, 12 monthsstandardized self-report measure of dementia knowledge, including knowledge of modifiable risk factors for ADRDClinicalTrials.gov
SecondaryMotivation to Change Behavior for Dementia Risk Reduction (MOCHAD-10)baseline, 2 months (end of treatment), 4 months, 12 monthsself-report measure of self-efficacy pertaining to behaviors for dementia risk reductionClinicalTrials.gov
SecondaryBody Weightbaseline, 2 months (end of treatment), 4 months, 12 monthsbody weightClinicalTrials.gov
SecondaryWaist circumferencebaseline, 2 months (end of treatment), 4 months, 12 monthswaist circumference (cm)ClinicalTrials.gov
SecondaryLipid panelbaseline, 2 months (end of treatment), 4 months, 12 monthsObtained via fasting blood draw. Total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides.ClinicalTrials.gov
SecondarySystolic blood pressurebaseline, 2 months (end of treatment), 4 months, 12 monthssystolic blood pressure (average of 3 measurements)ClinicalTrials.gov
SecondaryHemoglobin A1Cbaseline, 2 months (end of treatment), 4 months, 12 monthsGlycated hemoglobin, a measure of average blood sugar over the past 2-3 monthsClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)