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

ConditionLiver Cancer

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age18+

SponsorM.D. Anderson Cancer Center

About this trial

To develop and test liver cancer prevention educational material.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

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

Disqualifiers

Has been diagnosed with liver cancer

Cannot provide consent or otherwise participate in research activities (e.g. vision or hearing impairment)

Trial population

Participants at HOPE Clinic

Trial design

Design model

Ecologic or community

Time perspective

Cross-sectional

Treatments tested in this trial

Cognitive Testing
Behavioral
Given by Survey and one-on one interviews
Usability Testing
Behavioral
Given by surveys and one-on-one interview.

Treatment groups

40 Participants

are divided into 2 treatment groups

Group A: Cognitive Interviews (English and Spanish)1 intervention

Group B: Usability Testing (English and Spanish)1 intervention

Trial outcomes

Primary outcomes

Cognitive Testing

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.

Time frame

Up to 1.5 hours

Usability Testing

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.

Time frame

Up to 1.5 hours

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

M.D. Anderson Cancer Center

Lead sponsor

Cancer Prevention Research Institute of Texas

Collaborator

Source ClinicalTrials.gov

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