Sensory and Physical Reactions to Beverage Cues
Part of paid clinical trials in Dallas, Texas.
- Sponsor
- University of Texas Southwestern Medical Center
- Study ID
- NCT07788716
- Status
- Recruiting
Conditions
- Alcohol Use Disorder (AUD)
Eligibility Criteria
- Sex
- ALL
- Age
- 21 Years - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Alcohol Cue Reactivity Paradigm — BEHAVIORALStandardized 3-minute visual, olfactory, and tactile exposure to beverage cues (water, and two similar appearing beverages) accompanied by guided audio instructions.
Study Details
The goal of this clinical trial is to evaluate changes in craving and sensory responses to different beverage cues in adults (aged 21-70) with current mild or greater alcohol use disorder (AUD). The main questions it aims to answer are: * Does exposure to different beverage cues elicit distinct changes in subjective craving? * How do beverage liking, peak craving, and the return of craving to baseline compare across different test-beverage conditions? Researchers will compare Session A (Test Beverage Condition A) to Session B (Test Beverage Condition B) in a randomized crossover design to see if sensory and expectancy effects influence craving responses without consumption. Participants will: * Complete two separate 3-minute cue reactivity trials per session (a baseline water cue, followed by a test-beverage cue) while listening to guided audio instructions and holding/smelling the beverage without drinking it. * Rate their craving and beverage liking using visual analog scales (VAS) immediately after each trial. * Provide breathalyzer readings (BrAC), vital signs, and safety/medication checks at both study visits. * Complete diagnostic and drinking history assessments (such as the SCID-5, TLFB, and ACQ-SF-R).
Key Dates
- First listed
- Aug 26, 2026
- Start date
- Oct 31, 2026
- Status verified
- Aug 2026
- Primary completion
- Oct 31, 2027
- Completion
- Dec 31, 2027
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- OTHER
Arms
- Experimental: Beverage AExposure to a visually matched beverage to Beverage B
- Experimental: Beverage BExposure to a visually matched beverage to Beverage A
Primary Outcome Measure
Change in Subjective Alcohol Craving Score, Visual Analog Scale (VAS) [ Time Frame: Visit 1 (baseline) through Visit 2, an average of 1 week. ]
Central Contacts
- Paola R Sparagana, BS214-645-6950
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Univeristy of Texas Southwestern Medical Center | Dallas | Texas | 75390 |
Find similar trials in Dallas, TX
Related Studies
- Combining a Smartphone App With Medications to Manage Heavy DrinkingRecruiting · VA Office of Research and Development · Phoenix, Arizona
- Suvorexant for Treatment of AUD and PTSDPHASE2 · Recruiting · Pharmacotherapies for Alcohol and Substance Use Disorders Alliance · Los Angeles, California
- Pregnenolone Treatment for Alcohol Use Disorder and Major Depressive DisorderPHASE2 · Not Yet Recruiting · Sherwood Brown, MD, PhD · Dallas, Texas
- Alpha-1 Blockade for Alcohol Use Disorder (AUD)PHASE2 · Recruiting · Brown University · Providence, Rhode Island