grant

Advancing a biopsychosocial model of bedtime procrastination

Organization UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAHLocation SALT LAKE CITY, UNITED STATESPosted 16 Aug 2024Deadline 15 Aug 2026
NIHUS FederalResearch GrantFY202521+ years oldAdultAdult HumanAnxietyAwardBMIBMI percentileBMI z-scoreBehaviorBehavioralBody fatBody mass indexCardiometabolic DiseaseCardiometabolic DisorderCause of DeathCircadian DysregulationCircadian RhythmsCircadian desynchronyDevelopmentDevelopment and ResearchDiabetes MellitusDimensionsDiseaseDisorderFellowshipFoundationsGlycohemoglobin AGlycosylated hemoglobin AHb A1Hb A1a+bHb A1cHbA1HbA1cHealthHemoglobin A(1)IVGTTIndividualInformal Social ControlInterventionLightLiteratureMediatingMelatoninModelingNyctohemeral RhythmOver weightOverweightPathway interactionsPhotoradiationPublic HealthQuetelet indexR & DR&DReportingResearchRestRewardsRiskRisk FactorsRoleSamplingScientistSelf RegulationSleepSleep DeprivationSleep disturbancesStatistical MethodsTestingTimeTime StudyTrainingTwenty-Four Hour RhythmUnited Statesaberrant sleepadult youthadulthoodbiopsychosocialcardiometaboliccardiometabolic riskcardiometabolismcircadiancircadian abnormalitycircadian desynchronizationcircadian disruptioncircadian disturbancecircadian dysfunctioncircadian impairmentcircadian misalignmentcircadian processcircadian rhythmicitycostdaily biorhythmdeficient sleepdevelop therapydevelopmentaldiabetesdisease riskdisorder riskdisrupted sleepdisturbed sleepexposure to lightexposure to visible lightfall asleepglycemic controlhemoglobin A1cimpaired sleepinadequate sleepindexinginnovateinnovationinnovativeinsufficient sleepintervention developmentintravenous glucose toleranceintravenous glucose tolerance testirregular sleeplight exposurelight pollution exposurelongitudinal designlongitudinal experimental designlongitudinal research designlongitudinal study designmalleable riskmodifiable risknovelpathwayprogramsresearch and developmentskillssleep amountsleep behaviorsleep debtsleep deficiencysleep deficitsleep disruptionsleep durationsleep dysregulationsleep episodesleep habitsleep healthsleep hygienesleep insufficiencysleep intervalsleep lengthsleep losssleep onsetsleep periodsleep quantitysleep timesleep wellnesssleep/wake behaviorsleep/wake disruptionsleep/wake disturbancesocial rolestatistic methodstherapy developmenttime asleeptime during sleeptime in sleeptime spent asleeptime spent sleepingtraining opportunitytreatment developmentyoung adultyoung adult ageyoung adulthood
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Full Description

PROJECT SUMMARY
Cardiometabolic diseases are the leading cause of death in the United States. With rates of these diseases

rising, there is an urgent need to identify modifiable risk factors that contribute to cardiometabolic diseases. A

growing literature has shown that circadian disruption, including disturbances in the regularity of circadian activity

and misalignment of sleep to circadian activity, increases cardiometabolic disease risk. However, there is a

critical gap in our understanding of the sleep-related behaviors which lead to circadian disruption and subsequent

disease risk. Bedtime procrastination refers to the tendency to delay bedtime in the absence of external

obligations. Bedtime procrastinators often have late and irregular sleep timing and engage in behaviors that

increase evening light exposure, potentially serving to misalign and destabilize circadian rhythms. Through

circadian disruption and insufficient sleep, bedtime procrastination poses a risk to cardiometabolic health.

However, no research has investigated the role of bedtime procrastination in circadian disruption or

cardiometabolic health. Furthermore, to date, research on the mechanisms underlying bedtime procrastination

has centered on a single construct: self-regulation. However, emerging research suggests that there are two

distinct pathways leading to bedtime procrastination. The first pathway involves delaying bedtime due to

difficulties with disengaging from rewarding pre-sleep activities, and second involves delaying bedtime to avoid

pre-sleep anxiety. As intervention on the reward- and avoidance-driven pathways would require different

strategies, this lack of research represents a significant barrier to future research and treatment. Together, the

primary objective of this project is to advance a biopsychosocial model of bedtime procrastination. To accomplish

this objective, two studies will be conducted. The first study will evaluate the impact of bedtime procrastination

on circadian disruption (Aim 1) and the risk of bedtime procrastination to cardiometabolic health (Aim 2). Aims

1 and 2 will be evaluated in a sample of overweight individuals using innovative multidimensional assessment of

circadian disruption and cardiometabolic health over the course of a year. The second study seeks to elucidate

the roles of anxiety, reward, and self-regulation in the development of daily bedtime procrastination (Aim 3) using

an intensive longitudinal design in a large sample of young adults. This project will advance an integrated model

of bedtime procrastination. Given that nearly 75% of individuals report procrastinating their bedtime at least once

per week, and the extensive impact of this behavior on sleep health, bedtime procrastination likely has a

substantial impact on public health. Accordingly, this project will evaluate the impact of this behavior on circadian

disruption and cardiometabolic health. Furthermore, by elucidating the mechanisms that underly bedtime

procrastination, this project will lay the foundation for future research identifying treatment targets and developing

novel interventions for bedtime procrastination and circadian-sleep disturbances.

Grant Number: 5F31HL176119-02
NIH Institute/Center: NIH

Principal Investigator: Steven Carlson

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