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NCT07107152Completed

Effect of Static vs. Conversational AI-Generated Messages on Colorectal Cancer Screening Intent: a Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 7 Aug 2025

Brief summary (registry, in English)

The goal of this clinical trial is to assess whether messages generated by a large language model (LLM), including both static and conversational formats, can increase colorectal cancer (CRC) screening intentions among U.S. adults aged 45-75 who have never completed CRC screening. The main questions it aims to answer are: Do personalized, AI-generated messages increase the self-reported likelihood of completing a stool-based CRC screening test within 12 months? Do they also increase intent to undergo colonoscopy screening within 12 months? Researchers will compare four groups: (1) no message control, (2) expert-written patient education materials, (3) a single AI-generated persuasive message, and (4) a motivational interviewing-style AI chatbot. These comparisons will help assess whether a conversational format offers added benefit over static AI or expert-generated content. Participants will: Be randomly assigned to one of the four study arms Spend at least 3 minutes reading or interacting with their assigned material Complete pre- and post-intervention surveys assessing intent to receive CRC screening Receive messages tailored to their self-reported demographics, including age, political ideology, gender, education, community setting (urban, rural, suburb), self-reported health, and the last time they saw their PCP

Status (registry)
Completed
Study type
Interventional
Enrollment
915 (actual)
First submitted
30 Jul 2025
Start date
11 Jun 2025
Primary completion date
21 Jun 2025
Lead sponsor
University of Pennsylvania
NCT number
NCT07107152

What you commit to

  • Study type: Interventional
  • Participants enrolled: 915
  • From 11 Jun 2025 to the primary completion date, 21 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous colonoscopy, stool test, sigmoidoscopy, or CT colonography

Other illness

  • Failure to pass pre- or post-intervention attention checks

Other

  • Identified as non-human respondents by reCAPTCHA or other automated bot detection
  • Completion time significantly shorter than the median, indicating inattentiveness

Who the study is looking for

  • Adults aged 45 to 75 years
  • Currently residing in the United States
  • Self-reported no prior colorectal cancer screening (or unsure if screened)
  • Able to read and understand English
  • Consent to participate in a behavioral research study

Age in the registry: 45 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Participants are recruited online via Prolific
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.