Decreasing the Temporal Window in Individuals With Alcohol Use Disorder

NCT04128761 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 124

Last updated 2025-12-17

Study results available
· View outcomes & findings →

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.

Conditions

Interventions

BEHAVIORAL

Scarcity Narrative

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

BEHAVIORAL

Neutral Narrative

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

Sponsors & Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

    collaborator NIH
  • McMaster University

    collaborator OTHER
  • Arizona State University

    collaborator OTHER
  • Carilion Clinic

    collaborator OTHER
  • University of Kentucky

    collaborator OTHER
  • Virginia Polytechnic Institute and State University

    lead OTHER

Principal Investigators

  • Stephen M LaConte, PhD · Fralin Biomedical Research Institute at VTC

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-21
Primary Completion
2024-05-28
Completion
2024-05-28

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04128761 on ClinicalTrials.gov