Skip to Main Content
Phase Pilot

The Effect of Acute Stress and Inflammation on Drinking

  • Study HIC#:2000028772
  • Last Updated:02/02/2024

The purpose of this study is to find out about the effects of acute stress and inflammation on responses to alcohol and alcohol consumption. The proposed study will fill a major gap in our understanding of stress, inflammation and alcohol consumption. This study is not designed to provide treatment to decrease alcohol use.

  • Age21 years - 65 years
  • GenderBoth

Contact Us

For more information about this study, including how to volunteer, contact:

Terril Verplaetse

Help Us Discover!

You can help our team find trials you might be eligible for by creating a volunteer profile in MyChart. To get started, create a volunteer profile, or contact helpusdiscover@yale.edu, or call +18779788343 for more information.

Trial Purpose and Description

The purpose of this study is to find out about the effects of acute stress and inflammation on responses to alcohol and alcohol consumption. The proposed study will fill a major gap in our understanding of stress, inflammation and alcohol consumption. This study is not designed to provide treatment to decrease alcohol use.

Eligibility Criteria

Inclusion criteria:

  1. Age 21-65;
  2. Able to read and write English;
  3. Meets DSM-5 criteria for current (past 6 months) moderate to severe alcohol use disorders;
  4. Drinking criteria: Males - Drinks > 14 drinks per week and exceeds 4 drinks per day at least twice per week; Females -Drinks > 7 drinks per week and exceeds 3 drinks per day at least twice per week.
  5. Must meet drinking criteria during a consecutive 30-day period within the 90 days prior to baseline;
  6. Laboratory sessions will be scheduled such that subjects will not have major responsibilities on the following day which might limit drinking during the self-administration session (e.g., job interview, exam);
  7. Negative urine pregnancy test for women.

Exclusion criteria:

  1. Participants with any significant current medical conditions (neurological, cardiovascular [including hypertension or hypotension: sitting BP >160/100 or <90/60mmHg at baseline screening], endocrine, thyroid, renal, liver), seizures, delirium or hallucinations, or other unstable medical conditions including HIV;
  2. Current DSM-5 substance use disorders, other than alcohol or nicotine;
  3. A positive test result at intake appointment on urine drug screens conducted for illicit drugs, excluding cannabis;
  4. Past 30 day use of psychoactive drugs including anxiolytics and antidepressants;
  5. Women who are pregnant or nursing, or fail to use one of the following methods of birth control unless she or partner is surgically sterile or she is postmenopausal (hormone contraceptives [oral, implant, injection, patch, or ring], contraceptive sponge, double barrier [diaphragm or condom plus spermicide], or IUD);
  6. Suicidal, homicidal or evidence of current (past 6-month) severe mental illness such as schizophrenia, bipolar disorder or major depression, or anxiety disorders;
  7. Subjects treatment-seeking or who are currently in treatment for alcohol use;
  8. Subjects with medical conditions contraindicating alcohol use (e.g., liver enzymes ≥3× normal);
  9. Subjects likely to exhibit clinically significant alcohol withdrawal during the study. We will exclude subjects who a) have a history of perceptual distortions, seizures, delirium, or hallucinations upon withdrawal, or b) have a score of > 8 on the Clinical Institute Withdrawal Assessment scale at intake appointments;
  10. Participation within the past 8 weeks in other studies that involve additive blood sampling and/or interventional measures that would be considered excessive in combination with the current application.
  11. Subjects >38 on the Alcohol Use Disorders Identification Test (AUDIT);
  12. Subjects with resting pulse >100 at challenge;
  13. Subjects with recent (past 2 weeks) acute illness or vaccination;
  14. Subjects with >Grade 2 laboratory abnormalities on screening, based on appropriate grading scale based on page 26-27

Principal Investigator

Sub-Investigators

For more information about this study, including how to volunteer, contact: