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Exploring the Decision to Drink (More) Alcohol Following Manipulations of Stress and Social Context (DoraR00)

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University of Washington

Status

Not yet enrolling

Conditions

Psychological Stress
Social Interaction

Treatments

Other: Stress
Other: Social Context

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT07390084
STUDY00023737
R00AA030591 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This preregistration documents an experiment examining the effects of acute stress and social context on alcohol-related decision-making. The study uses a 2x2 factorial design (stress vs. control × social vs. alone) with dyadic recruitment.

Full description

Behavioral data:

Our first set of hypotheses tests whether the decision is influenced by stress and social context:

H1a: Stress affects the decision between alcoholic and non-alcoholic drinks, so that participants in the stress conditions choose alcoholic over non-alcoholic drinks more often compared to participants in the no stress conditions.

H1b: Social context affects the decision between alcoholic and non-alcoholic drinks, so that participants in the social conditions choose alcoholic over non-alcoholic drinks more often compared to participants in the alone conditions.

H1c: We test two competing predictions:

(I) The effect of stress on the decision between alcohol and non-alcoholic drinks is modulated by social context, so that the effect of stress is stronger for participants that are in the social condition.

(II) The effect of stress on the decision between alcohol and non-alcoholic drinks is modulated by social context, so that the effect of stress is weaker for participants that are in the social condition

Drift diffusion modeling:

Our second set of hypotheses test how the decision might be influenced by stress and social context:

H2a: Stress affects the bias (but not the drift rate or boundary) parameter of the drift diffusion model, so that the bias parameter is more positive for participants in the stress conditions.

H2b: Social context affects the bias (but not the drift rate or boundary) parameter of the drift diffusion model, so that the bias parameter is more positive for participants in the social conditions.

H2c: Stress and social context have an interactive effect on the bias (but not the drift rate or boundary) parameter of the drift diffusion model, so that the bias parameter is either more or less positive for stressed participants who are in the social condition (in line with H1c).

Enrollment

160 estimated patients

Sex

All

Ages

21 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Drinking alcohol at least once a week
  • Consuming 4 (female) or 5 (male) drinks in one occasion at least once a month

Exclusion criteria

  • Currently pregnant or trying to become pregnant
  • Past or current treatment for alcohol use
  • Past or current medical condition that contraindicates alcohol use
  • Past or current reaction to alcohol that contraindicates alcohol use
  • Past or current medication that contraindicates alcohol use

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

160 participants in 4 patient groups

Stress Alone
Experimental group
Description:
These participants will undergo a stress induction and will make decisions about consuming alcohol alone.
Treatment:
Other: Stress
Stress Social
Experimental group
Description:
These participants will undergo a stress induction and will make decisions about consuming alcohol with a known peer.
Treatment:
Other: Social Context
Other: Stress
Control Alone
Experimental group
Description:
These participants will undergo a control induction and will make decisions about consuming alcohol alone.
Treatment:
Other: Social Context
Other: Stress
Control Social
Experimental group
Description:
These participants will undergo a control induction and will make decisions about consuming alcohol with a known peer.
Treatment:
Other: Social Context

Trial contacts and locations

0

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Central trial contact

Jonas Dora

Data sourced from clinicaltrials.gov

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