Prostate Cancer Clinical Trial
Official title:
Evaluation and Management for Prostate Oncology, Wellness, and Risk (EMPOWeR)
| NCT number | NCT03807492 |
| Other study ID # | 18D.644 |
| Secondary ID | |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | January 16, 2019 |
| Est. completion date | February 7, 2024 |
| Verified date | March 2024 |
| Source | Thomas Jefferson University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
The EMPOWeR study is proposed as a cohort study with longitudinal follow-up to determine rates of genetic mutations among men with or at-risk for prostate cancer to address the various facets of genetic education and counseling for optimized genetic assessment and wellness of men. The results will inform practice guidelines and future studies for maximal impact of genetic evaluation of men for inherited prostate cancer.
| Status | Completed |
| Enrollment | 241 |
| Est. completion date | February 7, 2024 |
| Est. primary completion date | June 1, 2022 |
| Accepts healthy volunteers | No |
| Gender | Male |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Men with a personal history of prostate cancer - Unaffected males who are at higher risk for prostate cancer (family history of prostate cancer or African American males) - Men who previously tested positive for a mutation may be eligible for Specific Aims 2-7 - Men with a known familial mutation - Men who previously participated in the Genetic Evaluation of Men (GEM) study (IRB#14S.546) will be offered participation in EMPOWeR - Exclusion Criteria: - Age < 18 years - Mental or cognitive impairment that interferes with ability to provide informed consent |
| Country | Name | City | State |
|---|---|---|---|
| United States | Thomas Jefferson University | Philadelphia | Pennsylvania |
| Lead Sponsor | Collaborator |
|---|---|
| Sidney Kimmel Cancer Center at Thomas Jefferson University |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Perform genetic testing for men with or at-risk for prostate cancer to determine association of mutations to patient characteristics. | Participants will undergo gene panel testing through a saliva or blood sample. A genetic test summary will be generated to give to participants at disclosure of results. Participants will receive genetic test results in person, by phone or via telehealth. Fisher's exact test will be used to determine association of mutations and variants to patient characteristics. | 6 months |
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