Developing an Educational Tool for Liver Cancer Prevention

This study aims to create and test an educational website to help people learn about preventing liver cancer. We are looking for 40 participants to help us make sure the information is easy to understand and the website is easy to use. You will participate in activities called Cognitive Testing and Usability Testing. Cognitive Testing checks if the text is clear, and Usability Testing checks if the website functions well. We want to make sure you can easily understand the information, input your risk factors, and download a personal summary. This study is for adults aged 18 and older who can speak and read English or Spanish, and can use a smartphone or computer. You cannot have a diagnosis of liver cancer to participate.

Study design
This is an observational study with a planned enrollment of 40 participants. The study does not specify a phase.
What's involved
You will participate in surveys and one-on-one interviews for up to 1.5 hours for Cognitive Testing and Usability Testing.
Compensation
Not stated in the trial record.
Follow-up
Not specified.

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NCT07010315

Development and Testing of a Patient-facing Educational Tool About Liver Cancer Prevention

Recruiting
Not specifiedAges 18+Observational
M.D. Anderson Cancer Center
~40 participants
Updated 2026-08-06 on ClinicalTrials.gov
What's tested:Cognitive TestingUsability Testing

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Cognitive Testing
Measured over Up to 1.5 hours
+1 more outcome measured
Liver Cancer
1 sites across 1 states
Texas1
  • Jessica Hwang, MD, MPH · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

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Eligibility criteria

Inclusion

At least 18 years old
Participants at the HOPE Clinic
Able to speak and read either English or Spanish
For usability testing: Able to use and navigate websites on own smart phone or study computer

Exclusion

Has been diagnosed with liver cancer
Cannot provide consent or otherwise participate in research activities (e.g. vision or hearing impairment)
  • Cognitive TestingUp to 1.5 hours

    Participant comprehension will be measured qualitatively through cognitive testing. In cognitive testing interviews, participants are asked to "think aloud" as they review and react to new information. Participants will be presented with the storyboard (mock-up) versions of the content and asked to describe in their own words what the information means to them. Cognitive interviews may include questions about content such as length, clarity of the language, and helpfulness of the educational material. A trained research team member will ask probing questions throughout interviews as needed. Based on patient feedback, modifications will be made iteratively to the content to ensure the content is understood and interpreted as intended. There is no post-survey for cognitive testing.

  • Usability TestingUp to 1.5 hours

    Usability will be measured qualitatively using a Usability Interview Guide. Usability will also be measured using the System Usability Scale. Acceptability will be measured with the Ottawa Acceptability Measures. Knowledge will be measured pre- and post- session using knowledge questions developed by the investigators and refined during cognitive testing.