Liver Cancer Community Education

February 21, 2024 updated by: Fox Chase Cancer Center

LIVE-R Life: Liver Cancer Education

This study proposes to bridge the gap between evidence and action and combat rising liver cancer rates attributed to Hepatitis B and C infection in Philadelphia by identifying neighborhoods with higher than expected rates of liver cancer and related risk factors and administering an educational intervention about liver cancer and neighborhood health in those communities, working with existing community partners at Fox Chase Cancer Center.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

67

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19111
        • Fox Chase Cancer Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Speaks/reads English
  • Lives in Philadelphia or receives healthcare at a community partner site in Philadelphia

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Liver Cancer Education
A health educator will present participants with a 30-minute PowerPoint presentation containing educational information about liver cancer risk, screening, prevention, symptoms, and treatments, as well as introduce the concept of neighborhood health (e.g., rates of liver cancer and related risk factors in a census tract and how that might influence individual cancer risk).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in mean liver cancer knowledge
Time Frame: Baseline, 30 minutes
Liver cancer knowledge will be measured through four true/false items. Responses will be summed for a total liver cancer knowledge score. A positive change in mean knowledge score indicates liver cancer knowledge increased from baseline to post-intervention.
Baseline, 30 minutes
Change in general interest in learning about neighborhood health
Time Frame: Baseline, 30 minutes
General interest in learning about neighborhood health will be measured through a single item asking, on a scale from strongly agree to strongly disagree, whether the participant would like to learn about liver cancer in their own neighborhood. A positive change in mean score indicates that interest increased from baseline to post-intervention.
Baseline, 30 minutes
Change in interest in learning about neighborhood health from a healthcare provider
Time Frame: Baseline, 30 minutes
Interest in learning about neighborhood health from a healthcare provider will be measured through a single item asking, on a scale from strongly agree to strongly disagree, whether the participant would like to learn about liver cancer in their own neighborhood from their doctor. A positive change in mean score indicates that interest increased from baseline to post-intervention.
Baseline, 30 minutes
Change in interest in learning about neighborhood health from other sources
Time Frame: Baseline, 30 minutes
Interest in learning about neighborhood health from other sources will be measured through a single item asking, on a scale from strongly agree to strongly disagree, whether the participant would like to learn about liver cancer in their own neighborhood from non-medical sources (e.g., website or brochure). A positive change in mean score indicates that interest increased from baseline to post-intervention.
Baseline, 30 minutes
Change in interest in discussing high liver cancer risk with a healthcare provider
Time Frame: Baseline, 30 minutes
Interest in discussing high liver cancer risk with a healthcare provider will be measured through a single item asking, on a scale from strongly agree to strongly disagree, whether the participant would be likely to discuss their liver cancer risk with a doctor if they learned they lived in a high-risk area. A positive change in mean score indicates that interest increased from baseline to post-intervention.
Baseline, 30 minutes
Change in outcome expectancies for learning about neighborhood health - patient behavior
Time Frame: Baseline, 30 minutes
Patient outcome expectancies for learning about neighborhood health will be measured through a single item asking, on a scale from 0 (not at all) to 10 (very much), whether learning about neighborhood health will help the participant make health decisions. A positive change in mean score indicates that outcome expectancies increased from baseline to post-intervention.
Baseline, 30 minutes
Change in outcome expectancies for learning about neighborhood health - provider behavior
Time Frame: Baseline, 30 minutes
Provider outcome expectancies for learning about neighborhood health will be measured through a single item asking, on a scale from 0 (not at all) to 10 (very much), whether learning about neighborhood health will help the participant's healthcare provider make health decisions for them. A positive change in mean score indicates that outcome expectancies increased from baseline to post-intervention.
Baseline, 30 minutes
Change in intentions about communicating with healthcare provider - neighborhood prevalence of liver cancer
Time Frame: Baseline, 30 minutes
intentions about communicating with healthcare provider about neighborhood liver cancer will be measured through a single item asking, on a scale from very likely to not at all likely, how likely the participant is to discuss liver cancer in their neighborhood with their healthcare provider over the next 12 months. A positive change in mean score indicates that intentions increased from baseline to post-intervention.
Baseline, 30 minutes
Change in intentions about communicating with healthcare provider - liver cancer screening
Time Frame: Baseline, 30 minutes
intentions about communicating with healthcare provider about liver cancer screening will be measured through a single item asking, on a scale from very likely to not at all likely, how likely the participant is to discuss liver cancer screening with their healthcare provider over the next 12 months. A positive change in mean score indicates that intentions increased from baseline to post-intervention.
Baseline, 30 minutes
Change in intentions about communicating with healthcare provider - liver cancer risk
Time Frame: Baseline, 30 minutes
intentions about communicating with healthcare provider about liver cancer risk will be measured through a single item asking, on a scale from very likely to not at all likely, how likely the participant is to discuss their personal risk factors for liver cancer with their healthcare provider over the next 12 months. A positive change in mean score indicates that intentions increased from baseline to post-intervention.
Baseline, 30 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 11, 2020

Primary Completion (Actual)

April 6, 2023

Study Completion (Actual)

April 6, 2023

Study Registration Dates

First Submitted

February 13, 2020

First Submitted That Met QC Criteria

February 13, 2020

First Posted (Actual)

February 17, 2020

Study Record Updates

Last Update Posted (Estimated)

February 22, 2024

Last Update Submitted That Met QC Criteria

February 21, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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