Trial Information

Summary: Individualized Risk Information System (IRIS) for BRCA Carriers

The purpose of this study is to collect focus group feedback to revise a computerized health-care decision aid called Individualized Risk Information System (IRIS). Your participation in this study is expected to last about 2 hours.

Clinicians - You have been asked to participate in this focus group research study because you are a clinician (genetics counselor, medical geneticist, medical oncologist or surgical oncologist) who works with individuals who have/have had BRCA-associated breast cancer.

Patient/Patient Advocate - You have been asked to participate in this focus group research study because you have either had a BRCA-associated breast cancer or are a breast cancer patient advocate.

Patient Inclusion/Exclusion Criteria:

- See http://clinicaltrials.coh.org for additional information.

This site is run by CenterWatch, a publishing company that focuses on the clinical trials industry. The information provided in this service is designed to help patients find clinical trials that may be of interest to them, and to help patients contact the centers conducting the research. CenterWatch is neither promoting this research nor involved in conducting any of these trials.

Trial listings updated: May 5, 2008 at 3:32:33 PM