NCT07197723Toboroz
Study of How People Make Decisions About Prostate Cancer Risk
Effect of Polygenic Risk Modifiers on Decisions of BRCA1/2 Mutation Carriers at Risk for Prostate Cancer
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. júl. 10.
Rövid összefoglaló (regiszter, angolul)
The purpose of this study is to learn how people with BRCA1/2 mutations respond to genetic risk modifier testing. The researchers will learn more about how people make choices about their health care, including about methods to screen for prostate cancer. Researchers are also doing this study to learn about how the genetic risk modifier test affects people's thoughts and feelings.
- Állapot (regiszter)
- Toboroz
- Vizsgálattípus
- Megfigyeléses
- Résztvevők száma
- 150 (tervezett)
- Első benyújtás
- 2025. szept. 25.
- Kezdés
- 2025. szept. 25.
- Elsődleges befejezés
- 2027. szept.
- Fő szponzor
- Memorial Sloan Kettering Cancer Center
- Betegségek
- Prosztatarák
- NCT-szám
- NCT07197723
Mit vállalsz
- Vizsgálat típusa: Megfigyeléses
- Tervezett résztvevők: 150
- 2025. szept. 25. és az elsődleges befejezés (2027. szept.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
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Korábbi kezelés
- Any patient who has had a prostate biopsy within 36 months, according to clinician note (for individuals not presently receiving care at the study site, this information will be based on self-report)
Más betegség
- Major psychiatric illness or cognitive impairment that in the judgment of the study investigators or study staff would preclude study participation.
- Under active treatment for a malignancy. (Patients are eligible if they have a prior history of malignancy other than prostate cancer, as long as they are not currently undergoing active treatment for the malignancy) (for individuals not presently receiving care at the study site, this information will be based on self-report.)
- Enrolled in NCI study 19-C-0040 (Natural History of Men at High-Risk for Prostate Cancer) based on self-report
- Patients with a known pathogenic and/or likely pathogenic germline variant in any hereditary prostate cancer risk gene, excluding BRCA1 and/or BRCA2, including but not limited to: HOXB13, ATM, CHEK2, NBN, PALB2, MLH1, MSH2, MSH6, PMS2,RAD51C, RAD51D and TP53.
Egyéb
- Any patients who are unable to comply with the study procedures as determined by the study investigators or study staff.
Kiket keres a vizsgálat
- Documentation of Disease
- o Patients must not have prostate cancer (for individuals not presently receiving care at the study site, this information will be based on self-report.)
- Age between 45 - 70;
- Assigned male sex at birth for individuals not presently receiving care at the study site, this information will be based on self-report.)
- Completed full sequence or targeted genetic testing with a result confirmed in a clinically approved laboratory showing a BRCA1/2 likely pathogenic or pathogenic variant identified, or clinician note documents a BRCA1/2 likely pathogenic or pathogenic variant
- 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.(for individuals not presently receiving care at the study site, this information will be based on self-report.)
Életkor a regiszterben: 45 év – 70 év · Nem: csak férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
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| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Memorial Sloan-Kettering Cancer Center | New York | Egyesült Államok | Toboroz |
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