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Enrolling by invitation NCT07365813

Testing Alcohol Cancer Risk Messages

No phase Interventional Alcohol Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Text-only messages, AI-developed Neutral pictorial messages, AI-developed graphic pictorial messages.
Who it may be relevant to
Registry conditions: Alcohol, Cancer. Basic parameters: from 21 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Developing and Testing AI-Generated Messages on Alcohol and Cancer Risk: A Proof of Concept

Overview

Testing gain vs loss-framed messages to address drinking among cancer survivors

Interventions

  • Behavioral Text-only messages
    The study will test eight alcohol-cancer risk messages (four gain-framed and four loss-framed). Each message will be developed at three intensity levels (text-only, neutral image, and graphic image), yielding 24 total message stimuli.
  • Behavioral AI-developed Neutral pictorial messages
    The study will test eight alcohol-cancer risk messages (four gain-framed and four loss-framed). Each message will be developed at three intensity levels (text-only, neutral image, and graphic image), yielding 24 total message stimuli.
  • Behavioral AI-developed graphic pictorial messages
    The study will test eight alcohol-cancer risk messages (four gain-framed and four loss-framed). Each message will be developed at three intensity levels (text-only, neutral image, and graphic image), yielding 24 total message stimuli.

Primary outcome measures

  • Change in alcohol-cancer harm perception [Time frame: Within 15 minutes on a single online session - from before message exposure (pre-exposure) to after message exposure (post-exposure).]
  • Intention to Reduce Alcohol consumption [Time frame: Within 15 minutes on a single online session - from before message exposure (pre-exposure) to after message exposure (post-exposure).]
  • Commitment to a limited drinking goal in the next month [Time frame: Within 15 minutes on a single online session - from before message exposure (pre-exposure) to after message exposure (post-exposure).]
Secondary outcome measures (2)
  • Message perceived effectiveness [Time frame: One time (within 5 minutes) post-exposure evaluation.]
  • Message Receptivity [Time frame: One time (within 5 minutes) post-exposure evaluation.]

Eligibility criteria

Inclusion criteria

  • Age 21 years or older
  • Resident of the United States
  • Able to read and speak English
  • Diagnosed with one of the following cancers: mouth, throat, larynx, liver, colon, rectum, or breast
  • Current alcohol user (≥ 1 alcoholic drink in the past 30 days)

Exclusion criteria

  • Adults unable to consent
  • Individuals younger than 21
  • Not residing in the US
  • Non-alcohol users (<1 drink)
  • Less than 50% completion of the survey

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Factorial
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 1 center
  • University of Miami — Miami

Identifiers

NCT: NCT07365813 · 20250012

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗