Ovarian Cancer Clinical Trial

Evaluating an Alternative Clinical Genetics Cancer Care Delivery Model: A Pilot Study of Patient Outcomes

Summary

This study will evaluate patients' experiences with having gynecologic or prostate medical oncologists and surgeons offer them genetic testing, and having genetic counselors return the test results to patients over the telephone. This is different from the usual approach to genetic testing, where gynecologic or prostate medical oncologists and surgeons refer their patients to a genetic counselor in order to have these tests done, and the genetic counselors return the test results to the patient in person or over the telephone. The investigators will only be evaluating this alternative way of providing genetic testing to ovarian or prostate cancer patients.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

MSK patient age 18 years or older.
Diagnosed with or presumed by physician to have prostate cancer, or pancreatic cancer and recommended to undergo, currently undergoing, or having undergone active surveillance. (Patients with invasive epithelial ovarian cancer, peritoneal cancer, or fallopian tube cancer, or pancreas cancer are no longer eligible for inclusion as of Amendment 9. Patients with advanced prostate cancer who have not participated in active surveillance are no longer eligible for inclusion as of Amendment 10)
Deemed to be clinically appropriate for multiplex genetic testing by their physician.
Agreed to receive clinical multiplex genetic testing from their physician.
English-fluent; the surveys were designed and validated in English and are not currently available in other languages. Translation of questionnaires into other languages would require reestablishing the reliability and validity of these measures. Therefore, participants must be able to communicate in English to complete the surveys.

Exclusion Criteria:

Patients who do not or will not receive their ongoing cancer care at MSK.
Major psychiatric illness or cognitive impairment that in the judgment of the study investigators or study staff would preclude study participation.
Any patients who are unable to comply with the study procedures as determined by the study investigators or study staff.
For ovarian cancer patients only: patient insured by a payer that does not provide coverage for multiplex genetic testing as delivered in this protocol (e.g., Cigna, United Health Care, or Oxford, (because these payers require genetic counseling by a genetics professional prior to testing).

Study is for people with:

Ovarian Cancer

Estimated Enrollment:

1022

Study ID:

NCT02917798

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 3 Locations for this study

See Locations Near You

Memorial Sloan Kettering Basking Ridge
Basking Ridge New Jersey, , United States More Info
Maria Carlo, MD
Contact
646-422-4438
Maria Carlo, MD
Principal Investigator
Memorial Sloan Kettering Commack
Commack New York, 11725, United States More Info
Maria Carlo, MD
Contact
646-422-4438
Maria Carlo, MD
Principal Investigator
Memorial Sloan Kettering Westchester
Harrison New York, 10604, United States More Info
Maria Carlo, MD
Contact
646-422-4438
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Maria Carlo, MD
Contact
646-422-4438
Maria Carlo, MD
Principal Investigator
Memorial Sloan Kettering Rockville Centre
Rockville Centre New York, , United States More Info
Maria Carlo, MD
Contact
646-422-4438

How clear is this clinincal trial information?

Study is for people with:

Ovarian Cancer

Estimated Enrollment:

1022

Study ID:

NCT02917798

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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