Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT05677321

Individual Variations of Taste and Smell Perception in Alcohol Use Disorder (AUD)

Led by National Institute on Alcohol Abuse and Alcoholism (NIAAA) · Updated on 2025-10-24

475

Participants Needed

1

Research Sites

207 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Individual Variations of Taste and Smell Perception in Alcohol Use Disorder (AUD)

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals between 18 to 65 years of age
  • Diagnosis of AUD (for AUD group) or no diagnosis of AUD (for non-AUD group) confirmed by clinician
  • Able to provide their own consent
  • Able to read and understand English to complete questionnaires independently
Not Eligible

You will not qualify if you...

  • Diagnosis of morbid obesity (BMI > 40) or renal disease
  • History of chronic rhinitis, eating disorder, chronic upper respiratory infection, chronic allergic rhinitis, or nasal polyps within 6 months, or current daily use of nasal sprays
  • Altered cranial nerves related to taste and smell identified on neurological exam
  • Positive pregnancy test, currently pregnant, or breastfeeding
  • Use of hypoglycemic drugs
  • Currently taking medications known to inhibit taste response (GLP1 agonists)
  • Experiencing temporary loss or change of taste or smell (may be rescreened later)
  • Persistent loss of taste or smell due to COVID-19 or other reasons
  • Employment or close relation with NIAAA staff or study investigators
  • Claustrophobia
  • Presence of ferromagnetic metal in the head or eye (e.g., aneurysm clip, neural stimulator, cochlear implant, ocular foreign body)
  • Having an implanted cardiac pacemaker or auto-defibrillator
  • Using an insulin pump
  • Presence of irremovable body piercing
  • Pregnancy or breastfeeding during screening or study due to MRI risks

AI-Screening

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Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

C

Chiquita L West

CONTACT

P

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

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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