- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06885190
Multisensory Processing of Alcohol Cues in Young Adult Binge Drinkers
March 20, 2025 updated by: Rebecca Houston, Rochester Institute of Technology
Binge drinking is common among young adults and is related to many negative health outcomes including blackouts, risky sex, drunk driving, alcohol use disorder, and liver disease.
Understanding whether there are differences in how binge drinkers respond to alcohol-related cues and whether this is related to craving is important for improving interventions and treatments.
The proposed study will compare behavioral and neural processing of alcohol and non-alcohol cues in a single sensory modality (vision) with that of cues presented in multiple sensory modalities (vision, touch, and smell) with varying degrees of realistic appearance (images, virtual reality, real objects).
Participants will answer questionnaires related to their physical and mental health and recent alcohol and drug use.
Those eligible for the study will complete two in-person lab sessions.
During both sessions they will be asked to view a series of cues which will include images on a computer screen, objects presented in virtual reality, or real objects.
Sometimes these will be presented just visually and other times they will be combined with the presentation of specific smells or an object to touch.
Some of these cues will be alcohol-related and others will be neutral (non-alcohol-related).
Brainwave activity, as measured by the electroencephalogram (EEG), and reports of alcohol craving will be collected during these sessions.
It is expected that brainwave activity will be greatest in response to multisensory cues compared to that in response unisensory (visual only) cues.
It is also expected that young adults with a recent history of binge drinking will show the greatest brainwave activity in response to multisensory alcohol cues compared to social drinkers.
Binge drinkers will also report more alcohol craving in response to multisensory alcohol cues compared to social drinkers.
It is anticipated that brainwave responses will increase as the level of realism of the cues increases.
Binge drinkers will also show stronger brainwave and craving responses to multisensory alcohol cues presented as real objects.
Finally, binge drinkers will show lessened brain and craving responses when multisensory cues do not match compared to social drinkers.
For example, if a photo shows an alcoholic drink but the smell presented is not alcohol related, binge drinkers will show less attentive brain activity toward those mismatched cues.
Given that most alcohol cues in daily life are experienced across multiple senses simultaneously, results of this research will provide a better understanding of the relation between alcohol cue processing and craving, and will inform development of more effective programs for decreasing young adult risky drinking behavior.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Rebecca J Houston, PhD
- Phone Number: 585-475-5205
- Email: rjhgss@rit.edu
Study Contact Backup
- Name: Elena Fedorovskaya, PhD
- Phone Number: 585-475-6952
- Email: eafppr@rit.edu
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Participants will be recruited via social media advertisements, fliers posted on college campuses and in the community, and a departmental research participants group.
Description
Inclusion Criteria:
- ages 18 to 25 years old
- meet criteria for either the binge drinker or social drinker groups previously described
Exclusion Criteria:
- history of head injury involving loss of consciousness of 10+ minutes
- colorblindness
- hearing, tactile, olfactory or uncorrected vision deficits
- history of seizures
- neurological disorder diagnosis
- mental health history of psychosis or mania
- history of alcohol or substance use disorder diagnosis
- illicit drug use in the past 30 days
- changes to psychotropic medication type or dose in past 3 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Young Adult Binge Drinkers
Participants ages 18 to 25 with a history of binge drinking (at least 2 episodes of 5+ standard drinks per episode for males/4+ standard drinks per episode for females) in the past month and at least 4+/3+ (males/females) score on the Alcohol Use Disorder Identification Test.
|
|
Young Adult Social Drinkers
Participants ages 18 to 25 who report drinking alcohol at least once in the past month but no current history of a binge pattern (i.e., 2 or fewer drinks per episode) AND score less than 4/3 (males/females) on the Alcohol Use Disorder Identification Test.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Event-related Potential Amplitudes in Response to Alcohol and Neutral Cues
Time Frame: Baseline and follow-up (within 1 week)
|
Amplitude (magnitude) of electrocortical activity assessed in response to alcohol-related and neutral cues presented either visually or in visual-olfactory or visual-tactile combinations.
|
Baseline and follow-up (within 1 week)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Rebecca J Houston, PhD, Rochester Institute of Technology
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Hone-Blanchet A, Wensing T, Fecteau S. The use of virtual reality in craving assessment and cue-exposure therapy in substance use disorders. Front Hum Neurosci. 2014 Oct 17;8:844. doi: 10.3389/fnhum.2014.00844. eCollection 2014.
- Hill-Bowen LD, Riedel MC, Poudel R, Salo T, Flannery JS, Camilleri JA, Eickhoff SB, Laird AR, Sutherland MT. The cue-reactivity paradigm: An ensemble of networks driving attention and cognition when viewing drug and natural reward-related stimuli. Neurosci Biobehav Rev. 2021 Nov;130:201-213. doi: 10.1016/j.neubiorev.2021.08.010. Epub 2021 Aug 13.
- Connor JP, Kavanagh DJ, Andrade J, May J, Feeney GF, Gullo MJ, White AM, Fry ML, Drennan J, Previte J, Tjondronegoro D. Alcohol consumption in young adults: the role of multisensory imagery. Addict Behav. 2014 Mar;39(3):721-4. doi: 10.1016/j.addbeh.2013.11.023. Epub 2013 Dec 4.
- Kiyak C, Simonetti ME, Norton S, Deluca P. The efficacy of cue exposure therapy on alcohol use disorders: A quantitative meta-analysis and systematic review. Addict Behav. 2023 Apr;139:107578. doi: 10.1016/j.addbeh.2022.107578. Epub 2022 Dec 12.
- Mellentin AI, Skot L, Nielsen B, Schippers GM, Nielsen AS, Stenager E, Juhl C. Cue exposure therapy for the treatment of alcohol use disorders: A meta-analytic review. Clin Psychol Rev. 2017 Nov;57:195-207. doi: 10.1016/j.cpr.2017.07.006. Epub 2017 Jul 27.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
September 1, 2025
Primary Completion (Estimated)
November 1, 2026
Study Completion (Estimated)
February 1, 2027
Study Registration Dates
First Submitted
March 13, 2025
First Submitted That Met QC Criteria
March 18, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 20, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SRS00020124
- R15AA031579-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.