NCT07848906

Brief Summary

Alcohol increases the risk for at least seven cancers, yet recent estimates suggest only between one-third and one-half of US adults are aware of this risk. The current study aims to develop and test alcohol-cancer messages designed for a mass media public health campaign. The messages will be informed by theory-based constructs proximal to health behavior change (e.g., perceived likelihood/severity of harm, response efficacy). We will evaluate messages via an online, cross-sectional message testing randomized experiment. Participants will be US adults aged 21+ recruited from Qualtrics Panels.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
1,400

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2026

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

September 17, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 30, 2026

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Completed
Last Updated

September 30, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

September 17, 2026

Last Update Submit

September 23, 2026

Conditions

Keywords

Message testing experimentAlcohol risk messagesAlcohol and cancer

Outcome Measures

Primary Outcomes (1)

  • Perceived message effectiveness - effects perceptions

    A 3-item scale adapted from prior effects perception PME and substance use literature. After each message exposure, participants will be asked to respond to the following items: 1) This message discourages me from wanting to drink alcohol; 2) This message makes me concerned about the health effects of drinking alcohol; and 3) This message makes drinking alcohol seem unpleasant to me. Items will be assessed on a 5-point scale ranging from strongly disagree (1) to strongly agree (5). We will assess internal consistency using Cronbach's alpha. Assuming adequate measure reliability, we will average the items into a single composite PME measure.

    Day 1; post intervention exposure

Secondary Outcomes (11)

  • Drinking intentions

    Day 1; post intervention exposure

  • Message reactance

    Day 1; post intervention exposure

  • Non-alcoholic beer message perceptions

    Day 1; post intervention exposure

  • Perceived message effectiveness - message perceptions

    Day 1; post intervention exposure

  • Attitudes toward alcohol

    Day 1; post intervention exposure

  • +6 more secondary outcomes

Study Arms (7)

Perceived likelihood frame

EXPERIMENTAL

Exposure to two alcohol-cancer messages that convey the probability of experiencing a health harm (i.e., cancer) from a particular hazard (i.e., drinking alcohol). The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Harm reduction frame

EXPERIMENTAL

Exposure to two alcohol-cancer messages that encourage reducing how much alcohol people drink. The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Perceived severity frame

EXPERIMENTAL

Exposure to two alcohol-cancer messages that convey how serious getting alcohol-associated cancer will be. The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Response efficacy frame

EXPERIMENTAL

Exposure to two alcohol-cancer messages that emphasize the effectiveness of protective behaviors for reducing alcohol-associated cancer risk. The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Harm prevention frame

EXPERIMENTAL

Exposure to two alcohol-cancer messages that emphasize completely abstaining from drinking alcohol. The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Surgeon General's frame

ACTIVE COMPARATOR

Exposure to two alcohol-cancer messages that do not discuss alcohol-associated cancer risk. Instead, the messages use language from the existing U.S. Surgeon General's warning on alcoholic beverages. The intervention will be administered in an online survey experiment as static images displayed to participants.

Behavioral: Alcohol health harm message exposure

Control

NO INTERVENTION

Participants randomized to control will not be exposed to any message stimuli.

Interventions

Randomized exposure to one of five alcohol-cancer health campaign message frames, or a non-cancer alcohol harms frame.

Harm prevention frameHarm reduction framePerceived likelihood framePerceived severity frameResponse efficacy frameSurgeon General's frame

Eligibility Criteria

Age21 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • currently reside in the US;
  • be aged 21 years or older; and
  • speak English.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neoplasms

Interventions

Ethanol

Intervention Hierarchy (Ancestors)

AlcoholsOrganic Chemicals

Central Study Contacts

Jacob A Rohde, PhD, MPH

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 17, 2026

First Posted

September 30, 2026

Study Start

September 1, 2026

Primary Completion

October 1, 2026

Study Completion

October 1, 2026

Last Updated

September 30, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will share

We will share anonymized IPD with researchers upon reasonable request to the project Principal Investigator.

Time Frame
IPD will be available on an ad hoc basis upon reasonable request for at least three years after the experiment is completed.
Access Criteria
Other researchers who provide a reasonable request about how they will use the data (e.g., validation, secondary analyses, etc).