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Recruiting NCT05675332

Effects of Stereotype Threat on Impulsivity and Its Relation to Alcohol Use in African Americans: An fMRI Study

No phase Interventional Alcohol Drinking

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Task-based behavioral intervention, Task-based behavioral intervention.
Who it may be relevant to
Registry conditions: Alcohol Drinking. Basic parameters: 21 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this study is to investigate the behavioral and neural correlates of stress exposure. Results from this study will enrich the understanding of how sociocultural, behavioral, and neural factors combine to influence alcohol use.

Interventions

  • Behavioral Task-based behavioral intervention
    Brief behavioral intervention is absent of stressors.
  • Behavioral Task-based behavioral intervention
    Brief behavioral intervention involves interacting with common everyday types of stress.

Primary outcome measures

  • Blood oxygen-level dependent (BOLD) signal [Time frame: Baseline]
  • Resting-state functional connectivity in brain regions [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Between 21 and 35 years of age (inclusive);
  • Fluent in English;
  • Right-handed

Exclusion criteria

  • Younger than 21 years of age;
  • Left-handed

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Basic science

Study locations

United States · 1 center
  • Icahn School of Medicine at Mount Sinai — New York

Identifiers

NCT: NCT05675332 · GCO 19-0250 · R01AA028023

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗