A rigorous test of dual process model predictions for problematic alcohol involvement
Project Number5R01AA030914-02
Contact PI/Project LeaderBARTHOLOW, BRUCE D Other PIs
Awardee OrganizationUNIVERSITY OF IOWA
Description
Abstract Text
Abstract
Problematic alcohol involvement (PAI), characterized by alcohol consumption that leads to or increases risk for
acute and/or chronic negative consequences in one or more life domains, poses an enormous public health
burden to drinkers, their families, and society. Heterogeneity in PAI’s etiology has been identified as the single
most important barrier to progress in remediating this burden. More effective characterization of neurobehavioral
traits that increase PAI risk is critical to the development of more effective intervention and prevention efforts.
Cognitive science approaches to addiction etiology have suggested PAI risk reflects an interaction between two
internal cognitive systems: appetitive motivation for alcohol (AMA) impelling alcohol seeking and use, and
executive function (EF) regulating the influence of appetitive drives. This Dual Process Model has been highly
influential, but prior studies have failed to support its main interaction hypothesis. We argue this failure is
attributable to weaknesses in the rigor of prior research, and propose several innovative refinements to the DPM
framework to improve its predictive utility. First, individual differences in AMA and EF have not been adequately
characterized in prior studies, most of which represent these constructs with single indicators. Innovations in
neuroclinical assessment indicate that neurobehavioral trait constructs are better characterized with measures
representing self-report, behavioral, and neurophysiological units of analysis. Second, DPMs assume risk for
PAI reflects only the influence of internal processes, implying no role for context. This is a major limitation, as
strong evidence indicates that both environmental contexts (e.g., legal constraints; alcohol access) and alcohol
exposure (e.g., acute effects of alcohol on EF and AMA) strongly affect the extent to which person-level factors
relate to PAI. Finally, given that PAI behaviors are the result of decisions people make while drinking, accounting
for heterogeneity in drinking-related decision strategies can improve prediction of PAI, including the role of DPM
constructs. We propose a multi-session, within-subject alcohol challenge experiment, combined with online
follow-up assessments, structured to take advantage of the abrupt change in contextual factors that occurs with
transition to the minimum legal drinking age (MLDA; i.e., 21st birthday). This transition broadly increases risk for
PAI within persons, but little is known about the role of specific etiologic factors in this increased risk. Participants
(N=220) will be recruited from rural census tracts in mid-Missouri, identified through state administrative and
driver’s license databases. Such individuals are broadly underrepresented in PAI research, particularly alcohol
challenge research, and tend to experience more chronic (less transient) and severe PAI than their relatively
advantaged, college-attending age peers. This sampling approach also will permit over-sampling of individuals
at higher risk for DUI arrest (e.g., based on parental history of DUI and area characteristics). Thus, this study will
fill important gaps in knowledge concerning PAI etiologic factors in an understudied population.
Public Health Relevance Statement
Project Narrative
The proposed study will test of the influence of two individual difference factors, motivation for alcohol and
cognitive control, on alcohol use and problems in young adults making the transition to legal drinking (i.e., the
21st birthday). The study will examine how these processes contribute to the increase in alcohol problems,
especially alcohol-impaired driving, that is known to occur in the year after the 21st birthday. Knowledge gained
from this research will inform efforts to reduce alcohol-related problems in young adult drinkers.
NIH Spending Category
No NIH Spending Category available.
Project Terms
21 year oldAccountingAcuteAffectAgeAlcohol abuseAlcohol consumptionAlcoholsAreaBehaviorBehavioralCensusesCharacteristicsChronicCognitive ScienceDataDatabasesDecision MakingDesire for foodDevelopmentDrunk drivingEtiologyFailureFamilyHeterogeneityIndividualIndividual DifferencesInfluentialsIntoxicationKnowledgeLegalLicensingLifeLinkMeasurementMeasuresMethodologyMissouriModalityModelingMotivationOutcomeParticipantPatient Self-ReportPersonsPopulationPreventionProcessPublic HealthQuestionnairesRecording of previous eventsReportingResearchRiskRoleRuralSamplingSocietiesStructureTestingWorkaddictionalcohol availabilityalcohol consequencesalcohol effectalcohol exposurealcohol involvementalcohol related problemalcohol seeking behaviorcognitive controlcognitive systemcollegecontextual factorsdesigndrinkingdriving behavioreffective interventionexecutive functionexperienceexperimental studyfollow up assessmenthigh riskimprovedindexinginnovationminimum drinking agemultimodalityneurobehavioralneurophysiologypeerpredictive modelingrecruitremediationsobrietystandard measuretraityoung adult
National Institute on Alcohol Abuse and Alcoholism
CFDA Code
273
DUNS Number
062761671
UEI
Z1H9VJS8NG16
Project Start Date
20-September-2023
Project End Date
31-August-2028
Budget Start Date
01-September-2024
Budget End Date
31-August-2025
Project Funding Information for 2024
Total Funding
$662,533
Direct Costs
$618,634
Indirect Costs
$43,899
Year
Funding IC
FY Total Cost by IC
2024
National Institute on Alcohol Abuse and Alcoholism
$662,533
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5R01AA030914-02
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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History
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