Decreasing the Temporal Window in Individuals With Alcohol Use Disorder
RP1B
Reinforcer Pathology 1B: Decreasing the Temporal Window
2 other identifiers
interventional
124
1 country
1
Brief Summary
In the absence of sufficient monetary resources, individuals must attend to immediate, minimum needs (e.g., food, shelter). This constricts one's temporal window and engenders neglect of the future. In observational studies, scarcity is associated with higher rates of delay discounting. Additionally, socioeconomic status is inversely associated with alcohol use disorder and related problems. Experimentally, scarcity shortens attention, impedes cognitive function, and increases delay discounting in multiple populations. Moreover, scarcity increases demand for fast foods in the obese and increases craving for alcohol in problem drinkers. These data suggest that economic scarcity worsens both components of reinforcer pathology (delay discounting and alcohol overvaluation), thus increasing vulnerability to alcohol use disorder. However, studies investigating the effects of scarcity on alcohol demand discounting rate have been limited. The purpose of Aim 1b is to examine effects of decreasing the temporal window and its concomitant effects on alcohol valuation (demand, and craving) and delay discounting.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 10, 2019
CompletedFirst Posted
Study publicly available on registry
October 16, 2019
CompletedStudy Start
First participant enrolled
September 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 28, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 28, 2024
CompletedResults Posted
Study results publicly available
December 17, 2025
CompletedDecember 17, 2025
December 1, 2025
8 months
October 10, 2019
May 28, 2025
December 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Delay Discounting (DD) Rates
DD rates were measured using an adjusting amount task where participants were presented with hypothetical choices between smaller immediate or larger later amounts of money after a range of delays (1 day-25 years). Individual indifference points were calculated for each delay and then used to estimate DD rates for each participant using Mazur's (1987) equation: V = A/(1+kD), where V is the value of the indifference point, A is the amount of the larger delayed reward, k is the discounting rate, and D is the delay. Discounting rates (k) were then natural-logarithmically transformed (ln(k)). Higher ln(k) indicates steeper discounting and greater reward devaluation with increases in delay, while a lower ln(k) reflects shallower discounting and less reward devaluation with increases in delay. Changes in ln(k) were compared within-subjects between S1 and S2. Average ln(k) was calculated for each session (S1 and S2) in each condition (scarcity or neutral).
At the first session (S1; baseline measures) and Session 2 (S2; occurs approximately 2-3 days after S1)
Intensity of Alcohol Demand
Participants completed a hypothetical Alcohol Purchase Task where they had to indicate how many drinks they would purchase at different prices ($0 to $80 per drink). The number of drinks purchased at $0 was used to calculate the intensity of demand. Changes in intensity of alcohol demand were compared within-subjects between Session 1 and Session 2, and between narrative type (scarcity or neutral).
At the first session (S1; baseline measures) and Session 2 (S2; occurs approximately 2-3 days after S1)
Change in Alcohol Craving
A brief questionnaire (the Alcohol Urges Questionnaire) will be used to assess alcohol craving. The Alcohol Urges Questionnaire is an 8-item survey that produces scores between 8-56, where higher scores indicate greater craving. Change in alcohol craving will be compared within-subjects between Session 1 and Session 2. The scores will be compared between groups (arms) across sessions.
At the first session (S1; baseline measures) and Session 2 (S2; occurs approximately 2-3 days after S1)
Secondary Outcomes (1)
Change in Stress Appraisal Measure
Session 2 (occurs approximately 2-3 days after baseline [S1])
Study Arms (2)
Scarcity Narrative
EXPERIMENTALParticipants assigned to the scarcity group will be asked to listen and consider a hypothetical narrative about a sudden loss of resources.
Neutral Narrative
SHAM COMPARATORParticipants assigned to the neutral group will be asked to listen and consider a hypothetical narrative about a neutral change in resources.
Interventions
Participants are presented with a hypothetical scarcity narrative and asked to listen and consider the scenario.
Participants are presented with a hypothetical neutral narrative and asked to listen and consider the scenario.
Eligibility Criteria
You may qualify if:
- High-risk or harmful drinking (AUDIT\>15)
- years of age or older
- Desire to quit or cut down on their drinking, but do not have proximate plans to enroll in treatment for AUD during the study period
You may not qualify if:
- having a current unmanaged psychotic disorder
- reporting current pregnancy or lactation
- having dementia
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- McMaster Universitycollaborator
- Arizona State Universitycollaborator
- Carilion Cliniccollaborator
- University of Kentuckycollaborator
- Virginia Polytechnic Institute and State Universitylead
- National Institute on Alcohol Abuse and Alcoholism (NIAAA)collaborator
Study Sites (1)
Fralin Biomedical Research Institute at VTC
Roanoke, Virginia, 24016, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Stephen LaConte
- Organization
- Virginia Tech
Study Officials
- PRINCIPAL INVESTIGATOR
Stephen M LaConte, PhD
Fralin Biomedical Research Institute at VTC
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- BASIC SCIENCE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 10, 2019
First Posted
October 16, 2019
Study Start
September 21, 2023
Primary Completion
May 28, 2024
Study Completion
May 28, 2024
Last Updated
December 17, 2025
Results First Posted
December 17, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will share
- Time Frame
- Data will be made available upon request after dissemination of results.
- Access Criteria
- Data requests will be reviewed by the principal investigator and data will be shared with the expectation of acknowledgment of funding source and primary study team.
Investigators will adhere to all NIH requirements regarding data sharing. Participant data collected in this project will be de-identified and made available on a shared secured data repository. We will also share the analysis results. As part of this process, all investigators will be required to agree to the following conditions: 1) will adhere to the reporting responsibilities; 2) will not redistribute the data beyond the requesting individual and named collaborators; 3) will give appropriate acknowledgement; 4) will not use the data for commercial purposes; and 5) will obtain appropriate ethical approvals. Results from research conducted will be shared and disseminated, including: regular project meetings, annual meetings, symposia, workshops, and/or conferences for related groups. Manuscripts will be written and submitted for publication in peer-reviewed journals/conferences, following the NIH Public Access Policy guidelines. All necessary ethical approvals will be obtained.