NCT05677321

Brief Summary

Background: Alcohol use disorder (AUD) is the most common substance use disorder in the world. Long-term AUD can affect a person s sense of taste and smell. This natural history study will compare alcohol drinking behaviors and measures of taste and smell in people with and without AUD. Objective: To understand how alcohol use changes the senses of taste and smell. Eligibility: People aged 18 to 65 years with or without AUD. Design: Participants will be screened. They will have several tests to assess their smell and taste functions. They will answer questions about their eating, alcohol use, and smoking or vaping habits. Participants will have 2 study visits. They will give samples of blood, nasal mucous, saliva, stool, and urine. Their bodies will be measured. They will undergo a type of scan that uses X-rays to measure their body composition. They will complete taste measurements. They will taste liquids by swishing them in their mouth, without swallowing. Then, they will be asked what they can detect and which flavors they preferred. They will also complete smell measurements. They will be asked if they can identify strong odors on a metal wand. They will be asked to rate the intensity and pleasantness of odors. Their brain activity in the frontal regions will be measured while they smell various odors. For this, we will use a brain imaging tool called functional near infrared spectroscopy. They will have sensory testing. Sensations such as pressure, pinpricks, heat, or vibrations will be applied to their skin. Then, they will be asked what they felt. They will keep diaries. They will write down what they eat (for 3 days), the alcohol they drink (3 days), and how much they sleep (14 days). They will wear a wristwatch-like device that records their activity for 14 days.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
475

participants targeted

Target at P75+ for all trials

Timeline
18mo left

Started Jan 2024

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress61%
Jan 2024Dec 2027

First Submitted

Initial submission to the registry

January 7, 2023

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 10, 2023

Completed
12 months until next milestone

Study Start

First participant enrolled

January 9, 2024

Completed
4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

October 24, 2025

Status Verified

October 22, 2025

Enrollment Period

4 years

First QC Date

January 7, 2023

Last Update Submit

October 23, 2025

Conditions

Keywords

chemosensationPreferenceNatural History

Outcome Measures

Primary Outcomes (1)

  • Taste and smell measures, alcohol drinking behavior

    Compare individuals with AUD to those without AUD in measures of taste and smell and alcohol drinking behaviors.

    At enrollment

Secondary Outcomes (1)

  • Inflammatory markers, genotypes, microbiota, salivary and metabolic hormones, biological measures, and personal factors

    At enrollment

Study Arms (2)

Participants with AUD

Drink regularly (i.e., 2 or more drinks per day for at least 3 days per week in the past 12 months)

Participants without AUD

Does not drink regularly (less than 2 drinks per day for at least 3 days per week in the past 12 months)

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Participants will be recruited from the Washington D.C. area.

You may qualify if:

  • To be eligible to participate in this study, an individual must meet all the following criteria:
  • Individuals between 18 to 65 years of age. Although the age range of participants recruited in the NIAAA Natural History protocol is between 18-77 years, due to documented knowledge that taste and smell diminishes with age, we will limit age to this range.
  • Individuals with a diagnosis of AUD (for the AUD cohort) OR without a diagnosis of AUD (for the non-AUD cohort) per clinician assessment
  • Able to provide their own consent.
  • Due to the extensive questionnaires (administered in English language only) that participants must complete independently, fluency in the English language is needed. Hence, participants must be able to read and understand English.

You may not qualify if:

  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Diagnosis by a medical professional of morbid obesity or BMI \> 40 or renal disease.
  • Any history of chronic rhinitis, eating disorder, chronic upper respiratory infection, chronic allergic rhinitis, or nasal polyps in the last 6 months of screening, or current daily use of nasal sprays.
  • Altered cranial nerves associated with taste and olfaction identified by neurological evaluation during physical exam (screening visit).
  • Positive pregnancy test, currently pregnant or breastfeeding.
  • Hypoglycemic drug intake.
  • Currently using medications known to inhibit taste response (GLP1 agonists).
  • Currently experiencing temporary change/loss of taste and/or smell (individual may be rescreened when symptoms resolve).
  • Persistent loss of taste and/or smell due to COVID-19 or other reason.
  • NIAAA employees/staff or subordinates/relatives/co-workers of NIAAA employees/staff or study investigators.
  • claustrophobia
  • Ferromagnetic metal in the cranial cavity or eye, e.g., aneurysm clip implanted neural stimulator, cochlear implant, ocular foreign body.
  • Presence of implanted cardiac pacemaker or auto-defibrillator.
  • Individuals with an insulin pump.
  • Presence of an irremovable body piercing.
  • +1 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institutes of Health Clinical Center

Bethesda, Maryland, 20892, United States

RECRUITING

Related Links

MeSH Terms

Conditions

Alcoholism

Condition Hierarchy (Ancestors)

Alcohol-Related DisordersSubstance-Related DisordersChemically-Induced DisordersMental Disorders

Study Officials

  • Paule V Joseph, C.R.N.P.

    National Institute on Alcohol Abuse and Alcoholism (NIAAA)

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Paule V Joseph, C.R.N.P.

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
NIH
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 7, 2023

First Posted

January 10, 2023

Study Start

January 9, 2024

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

October 24, 2025

Record last verified: 2025-10-22

Locations