grant

The MyGoals for Healthy Aging Multi-Center Randomized Controlled Trial

Organization COLUMBIA UNIVERSITY HEALTH SCIENCESLocation NEW YORK, UNITED STATESPosted 1 Aug 2022Deadline 31 May 2027
NIHUS FederalResearch GrantFY2025AD dementiaAD related dementiaADRDAccelerationActive Follow-upAffectAgingAgreementAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer risk factorAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's and related dementiasAlzheimer's dementia and related dementiaAlzheimer's dementia or related dementiaAlzheimer's disease and related dementiaAlzheimer's disease and related disordersAlzheimer's disease or a related dementiaAlzheimer's disease or a related disorderAlzheimer's disease or related dementiaAlzheimer's disease related dementiaAlzheimer's disease riskAlzheimers DementiaAreaArtifactsAutoregulationBaltimoreBiological AgingBloodBlood GlucoseBlood Reticuloendothelial SystemBlood SugarBody SystemBrainBrain Nervous SystemC-reactive proteinCNS Nervous SystemCausalityCause of DeathCentral Nervous SystemCessation of lifeChronic DiseaseChronic IllnessCitiesCognitionCollaborationsCollectionConsentDNA MethylationDataData CollectionData SetDeathDecrease disparityDiabetes MellitusDietDisadvantagedDoctor of PhilosophyEconomic IncomeEconomical IncomeEconomicsEducational AchievementEducational StatusEmotionalEmploymentEncephalonEnsureEtiologyExecutive DysfunctionExecutive Function DeficitExecutive ImpairmentExerciseFaceFamilyFundingFutureGenesGoalsHealthHealth FoodHeightHistoryHomeostasisHousingHumanImpoverishedIncentivesIncomeIndividualInterventionLearningLifeLinkLonelinessLower disparityMaintenanceMeasurementMeasuresMethodsModelingModern ManMoodsMorphologic artifactsMotivationNational Institute of AgingNational Institute on AgingNerve CellsNerve UnitNeural CellNeuraxisNeurocyteNeuronsNutritionNutritious foodObesityOrgan SystemOutcomeOutcome MeasureParticipantPersonal SatisfactionPersonsPh.D.PhDPhysiological HomeostasisPilot ProjectsPopulationPovertyPrimary Senile Degenerative DementiaProcessProteins, specific or class, C-reactiveProtocolProtocols documentationPsychologic StressPsychological StressPublic HealthPublic HousingRandomized, Controlled TrialsRecording of previous eventsRisk FactorsSalivaSample SizeSamplingSection 8SiteSleepSocial FunctioningSocial PoliciesSocioeconomic FactorsStressSurvey InstrumentSurveysTestingTimeUnemploymentVisitWeightWorkaccelerated agingaccelerated biological ageaccelerated biological agingactive followupadiposityage accelerationaging associatedaging processaging relatedalzheimer riskauthoritybiological process of agecausationchronic disordercohortcorpulencedementia riskdesigndesigningdiabetesdietsdisease causationdisparity eliminationdisparity reductioneconomiceconomic outcomeeducational levelelectronic dataeliminate disparitieseliminating disparitiesexecutive controlexecutive functionfacesfacialfield based datafield learningfield studyfield testfollow upfollow-upfollowed upfollowupfunction sociallyfunctioning socialhealth datahealthy aginghealthy foodhealthy human aginghistoriesincomesinnovateinnovationinnovativeintervention effectjoblessjoblessnesslonelyloss of functionmeasurable outcomemethylation patternmitigate disparitymortalityneuronalnovelout of workoutcome measurementpace of agingpace of biological agingparent awardparent projectpilot studyprimary degenerative dementiaprogramsrandomized control trialrate of agingrate of biological agingreduce disparityreduction in disparityresponserisk factor for dementiarisk for dementiasample collectionscale upsenile dementia of the Alzheimer typeservice deliverysocio-economicsocio-economic factorssocio-economicallysocioeconomicallysocioeconomicsspecimen collectionspeed of agingspeed of the agingsuccesstraining achievementtraining leveltraining statustrial designunemployedvoucherweightswelfarewell-beingwellbeing
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Full Description

Poverty is associated with harsh living conditions, few opportunities to exercise, and poor access to healthy
food that collectively produce “wear and tear” on organ systems. Psychological stress increases the fragility of

neurons in the central nervous system, potentially producing both the loss of function and volume in areas of

the brain that are involved in maintaining homeostasis (e.g., blood glucose), planning tasks, executing tasks,

motivation, and emotional control. Psychological stress and poor nutrition can accelerate the aging process,

and may manifest as executive function deficits, diabetes, obesity, Alzheimer's disease/Alzheimer's disease-

related dementias (AD/ADRD), and early death. The mechanisms by which poverty-associated stress

accelerates aging are known, but there is no proven intervention to slow the rapid pace of aging among

impoverished families. Anti-poverty programs are a logical point of intervention.

An ongoing randomized-controlled trial (RCT), MyGoals for Employment Success, intervenes on both poverty

using proven employment incentives and on executive function deficits using a field-tested coaching program.

That study was designed to evaluate outcomes associated with executive function, economic well-being, and

social functioning. To evaluate outcomes associated with aging, additional intervention time and follow up are

needed because health outcomes tend to lag economic outcomes.

The National Institute on Aging provided one year of funding for cohort maintenance and to re-design MyGoals

for Employment Success into a healthy aging study with three years of intervention time, six years of follow up,

and health, aging, and cognition measures. This re-design was done in collaboration with leading

interdisciplinary experts using the Delphi method, a formalized process for understanding how to optimize

measure selection and the timing of measure collection. With their input, we propose an innovative RCT that

we call MyGoals for Healthy Aging. We will measure the effect of the intervention on psychological stress, diet,

sleep, mood, loneliness, height, weight, executive function, blood sugar, high-sensitivity C-reactive protein, and

gene methylation patterns. We will also store blood for future “freezer studies” that allow for more sophisticated

measures of human aging. In addition, we will maintain an ongoing dataset linked to electronic data so that it is

possible to measure outcomes beyond the time frame of the study, including future income and mortality by

cause of death. Completion of these aims will provide foundational evidence on the ability of social policy to

influence aging-related health outcomes; our ultimate goal is to test a novel intervention that might reduce or

eliminate disparities in chronic diseases including AD/ADRD.

Grant Number: 3R01AG073402-04S2
NIH Institute/Center: NIH

Principal Investigator: Daniel Belsky

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