Consumer Responses to Alcohol Warnings
1 other identifier
interventional
2,522
1 country
1
Brief Summary
The primary objective is to evaluate whether alcohol warnings about different topics elicit higher perceived message effectiveness than control messages. The secondary objective is to evaluate whether alcohol warnings about different topics elicit higher reactance than control messages.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2024
1 active site
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
First Submitted
Initial submission to the registry
November 27, 2023
CompletedFirst Posted
Study publicly available on registry
December 7, 2023
CompletedStudy Start
First participant enrolled
January 18, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 26, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 26, 2024
CompletedFebruary 13, 2024
February 1, 2024
8 days
November 27, 2023
February 9, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Perceived message effectiveness
The study will assess perceived message effectiveness using 1 item: "How much does this message discourage you from wanting to drink alcohol?" Response options will range from "not at all" (coded as 1) to "a great deal" (coded as 5). Higher scores indicate more perceived message effectiveness.
The survey will take up to 20 minutes.
Secondary Outcomes (1)
Reactance
The survey will take up to 20 minutes.
Study Arms (1)
Alcohol Messages
EXPERIMENTALParticipants view 12 messages: 10 messages related to health topics (2 messages for each of 5 randomly selected health topics from among all health topics) and 2 control messages.
Interventions
Participants will view messages about the risk of mouth cancer from alcohol consumption.
Participants will view messages about the risk of throat cancer from alcohol consumption.
Participants will view messages about the risk of voice box (larynx) cancer from alcohol consumption.
Participants will view messages about the risk of esophagus cancer from alcohol consumption.
Participants will view messages about the risk of liver cancer from alcohol consumption.
Participants will view messages about the risk of colon and rectum cancer from alcohol consumption.
Participants will view messages about the risk of breast cancer from alcohol consumption.
Participants will view messages about the risk of cancer (not site-specific) from alcohol consumption.
Participants will view messages about the risk of addiction and neurological changes from alcohol consumption.
Participants will view messages about the risk of hypertension from alcohol consumption.
Participants will view messages about the risk of liver damage from alcohol consumption.
Participants will view messages about the risk of harm to a fetus from alcohol consumption during pregnancy.
Participants will view messages about the risk of dementia from alcohol consumption.
Participants will view messages about the risk of impaired sleep from alcohol consumption.
Participants will view messages about guidelines for alcohol consumption.
Participants will view neutral messages unrelated to the harms of alcohol consumption.
Participants will view messages about the risk of road injuries from alcohol consumption.
Eligibility Criteria
You may qualify if:
- Age 21 and older
- Reside in the United States
- Able to complete a survey in English
You may not qualify if:
- Under 21 years of age
- Reside outside the United States
- Unable to complete a survey in English
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Online study
Palo Alto, California, 94304, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Anna Grummon, PhD
Assistant Professor
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
November 27, 2023
First Posted
December 7, 2023
Study Start
January 18, 2024
Primary Completion
January 26, 2024
Study Completion
January 26, 2024
Last Updated
February 13, 2024
Record last verified: 2024-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP, ANALYTIC CODE
- Time Frame
- Investigators will post IDP upon acceptance of any manuscripts associated with the data generated in this study.
- Access Criteria
- Data and code will be publicly available.
Investigators will post de-identified individual participant data in a publicly available repository.