- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04272619
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
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
- Name: Shannon M Lynch, PhD
- Phone Number: 215-728-5377
- Email: shannon.lynch@fccc.edu
Study Locations
-
-
Pennsylvania
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Philadelphia, Pennsylvania, United States, 19111
- Fox Chase Cancer Center
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-
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.
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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.
Sponsor
Collaborators
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19-1039
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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