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Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling

Li-Fraumeni Syndrome Clinical Trial

Official title:
Evaluate Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling Based on LFSPRO-ShinyApp Data

Clinical Trial Summary

This study evaluates patients willingness to participate in a trial comparing standard genetic counseling versus personalized genetic counseling. Collecting information from patients may help researchers learn why patients may or may not take part in the future study that compares standard genetic counseling to personalized genetic counseling.

Clinical Trial Description

PRIMARY OBJECTIVE: I. To evaluate patients' willingness to participate in a future randomized trial comparing standard genetic counseling versus personalized genetic counseling based on Li-Fraumeni syndrome patient reported outcome (LFSPRO) ShinyApp data. OUTLINE: Patients complete a questionnaire over 15-20 minutes. Patients positive for a TP53 mutation complete an additional questionnaire over 15-20 minutes within 1 month after test results. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05126810
Study type Observational
Source M.D. Anderson Cancer Center
Contact Banu Arun
Phone 713-792-2360
Email barun@mdanderson.org
Status Recruiting
Phase
Start date November 3, 2022
Completion date October 2, 2027
View Details
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