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The investigators will evaluate the feasibility of an intervention to improve Lynch syndrome cascade screening uptake. The investigators will conduct a pilot study among 15 patients diagnosed with Lynch Syndrome and 5 genetic counselors to assess the feasibility and intermediate outcomes of an educational workbook containing exercises and resources to improve family communication among individuals with Lynch Syndrome and first-degree relatives of individuals with Lynch Syndrome.
Genetic counselors of patients with Lynch Syndrome and patients with Lynch Syndrome will test a planning tool (referred to as an educational workbook) for cascade screening. Five genetic counselors and 15 patients with Lynch Syndrome will be recruited from the UNC Health System and the Ohio State Comprehensive Cancer Center. Genetic counselors will identify patients with Lynch Syndrome and introduce the study opportunity to potential patient participants. All patients and genetic counselors will complete a telephone enrollment call and provide informed consent to participate. Enrolled patients will work with enrolled genetic counselors to complete the first workbook exercise and then patients will complete the remaining exercises alone for over approximately 1 month. After genetic counselors and patients have completed using the workbook, the investigators will conduct qualitative virtual interviews over Zoom and a post-intervention electronic survey to understand the participants' experiences using the workbook. The investigators aim to understand the feasibility of using the workbook as an intervention in clinical practice to improve genetic testing uptake in families with Lynch Syndrome.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, United States
Start Date
August 1, 2021
Primary Completion Date
May 2, 2024
Completion Date
May 2, 2024
Last Updated
July 3, 2025
20
ACTUAL participants
Educational Workbook
BEHAVIORAL
Lead Sponsor
UNC Lineberger Comprehensive Cancer Center
Collaborators
NCT03050268
NCT06218433
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT04095195