Evaluating Cascade Communication Methods

Completed

Conditions studied: BRCA1 Mutation, BRCA2 Mutation

In brief

Hereditary cancer programs face challenges with respect to effective communication of genetic test results within families and uptake of genetic testing by relatives. This study aims to determine if a "disclosure toolkit" provided to the index participant (carrier of cancer risk gene mutation) contributes to sharing genetic test results with relatives, if there are preferred disclosure methods, and whether toolkit use contributes towards at-risk relatives pursuing genetic testing.

Key facts

Study ID
NCT04428736
Run by
University of Pennsylvania
People needed
52
Starts
2020-02-19
Expected to finish
2025-12-31
Last updated by the study team
2026-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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