NCT04128761

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
124

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 10, 2019

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 16, 2019

Completed
3.9 years until next milestone

Study Start

First participant enrolled

September 21, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 28, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 28, 2024

Completed
1.6 years until next milestone

Results Posted

Study results publicly available

December 17, 2025

Completed
Last Updated

December 17, 2025

Status Verified

December 1, 2025

Enrollment Period

8 months

First QC Date

October 10, 2019

Results QC Date

May 28, 2025

Last Update Submit

December 2, 2025

Conditions

Keywords

Delay DiscountingBehavioral Economic DemandScarcity NarrativeAlcohol Craving

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

EXPERIMENTAL

Participants assigned to the scarcity group will be asked to listen and consider a hypothetical narrative about a sudden loss of resources.

Behavioral: Scarcity Narrative

Neutral Narrative

SHAM COMPARATOR

Participants assigned to the neutral group will be asked to listen and consider a hypothetical narrative about a neutral change in resources.

Behavioral: Neutral Narrative

Interventions

Participants are presented with a hypothetical scarcity narrative and asked to listen and consider the scenario.

Scarcity Narrative

Participants are presented with a hypothetical neutral narrative and asked to listen and consider the scenario.

Neutral Narrative

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Fralin Biomedical Research Institute at VTC

Roanoke, Virginia, 24016, United States

Location

MeSH Terms

Conditions

Alcoholism

Condition Hierarchy (Ancestors)

Alcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Results Point of Contact

Title
Stephen LaConte
Organization
Virginia Tech

Study Officials

  • Stephen M LaConte, PhD

    Fralin Biomedical Research Institute at VTC

    PRINCIPAL INVESTIGATOR

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

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.

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.

Locations