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Chicago Social Drinking Project

Individual Differences After Consumption of Alcohol and Other Common Substances and Long-Term Follow-Up of Social Drinking, Young Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00961792
Acronym
CSDP
Enrollment
800
Registered
2009-08-19
Start date
2004-03-01
Completion date
2027-10-01
Last updated
2026-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcoholism

Brief summary

This study attempts to elucidate the factors that contribute to escalation and maintenance of excessive ethanol drinking in young adults by: 1. Examining subjective and objective response differences to alcohol and other common substances in a sample of adults with varying consumption patterns. 2. Determining whether response to alcohol and other substances is predictive of future consumption patterns through longitudinal follow-up interviews. 3. Examining the relationship between responses to alcohol and other substances at baseline and re-examination testing to evaluate if consumption patterns moderate this relationship.

Interventions

DRUGEthanol

Beverage containing 0.8 g/kg ethanol, 0.4 g/kg ethanol

DRUGPlacebo

Beverage containing 0.0 g/kg alcohol to act as placebo

DRUGDiphenhydramine

Beverage containing dose equivalent to 1.5 standard doses of Diphenhydramine (Benadryl)

DRUGCaffeine

Beverage containing the equivalent of 1.5 times the participant's daily caffeine intake

Sponsors

University of Chicago
Lead SponsorOTHER
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 21-65 * Weigh between 110-210 lbs * Drink alcohol at least once weekly with weekly "binge" drinking episodes * Available to complete in-person screening and 2, 4 hour experimental sessions at the University of Chicago * Available by phone, mail, or Internet for follow-up interviews for at least 2 years following sessions

Exclusion criteria

* Current or past major medical or psychiatric disorders including alcohol and substance dependence

Design outcomes

Primary

MeasureTime frame
Subjective response to alcohol and other common substances utilizing mood questionnaires in adult drinkersMeasured during 5 timepoints at each experimental session: 1) Pre-drink baseline, 2) +30 minutes, 3) +60 minutes, 4) +120 minutes, and 5) +180 minutes following the initiation of beverage consumption

Secondary

MeasureTime frame
Substance Use Behavior Reported During Follow-Up InterviewsMeasured at 3, 6, 9, 12, 15, 18, 21, 24, 36, 48, and 60 months following the final experimental session

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAndrea C King, PhD

University of Chicago

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 10, 2026