Actively Recruiting
Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling
Led by M.D. Anderson Cancer Center · Updated on 2026-04-15
500
Participants Needed
1
Research Sites
256 weeks
Total Duration
On this page
Sponsors
M
M.D. Anderson Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals age 15 or older or parent/guardian of a patient younger than 15 years (patients age 15-17 will provide assent and parent/guardian will provide consent)
- Pregnant women are allowed to participate
- Fluent in English
- Receiving genetic counseling specifically for TP53 genetic testing and consent to undergo TP53 genetic testing, or have a TP53 germline mutation
You will not qualify if you...
- Non-English speaking individuals
- Individuals with low suspicion for TP53 germline mutation during pretest counseling who test negative for TP53 mutation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
M D Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
B
Banu Arun
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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