Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 2:48 PM
Ignite Modification Date:
2025-12-24 @ 2:48 PM
NCT ID:
NCT03445559
Eligibility Criteria:
Inclusion Criteria:
Provider Criteria:
* Urology Chiefs and attending urologists employed through the VA (full time, part time) at one of the 10 participating sites
* Physician Assistants and Nurse Practitioners employed through the VA at one of the 10 participating sites that work in the respective urology clinics
* Providers may be any gender or race/ethnicity
Qualitative portion only:
* Urology Chiefs and/or frontline staff physicians
* participating PAs \& NPs having cared for at least 5 men with incident prostate cancer within the previous 6 months
* Patients will not be directly recruited into the study.
* The investigators have obtained a waiver of HIPAA authorization and informed consent to analyze electronic health records of patients that are diagnosed with ICD-9 code 185 or ICD-10 code C61 during the study period at the 10 participating sites.
Exclusion Criteria:
Provider Criteria:
* Urology Residents will be excluded.
Patients
* Patients will be excluded if they have a history of prior malignancy
* Are over the age of 85
* Diagnosed at autopsy or by death certificate
* Died within 3 months of diagnosis
* Not having data on at least one of the following:
* PSA
* clinical stage
* Gleason score
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT03445559
Study Brief:
Protocol Section:
NCT03445559