Patients
Item
for patients:
boolean
C0030705 (UMLS CUI [1])
Gender Fulfill NCCN Guidelines | Low risk Prostate carcinoma
Item
men who meet the nccn guidelines for low risk prostate cancer, which include all of the following:
boolean
C0079399 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C1513893 (UMLS CUI [1,3])
C0162791 (UMLS CUI [1,4])
C5201228 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
Gleason score | TNM clinical staging
Item
most recent gleason score ≤ 6, or clinical stage t1a or less;
boolean
C3203027 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
Prostate specific antigen measurement
Item
most recent psa level below 10;
boolean
C0201544 (UMLS CUI [1])
Core needle biopsy Positive Quantity | Malignant Neoplasm Percentage
Item
in the most recent biopsy, had fewer than 3 positive biopsy cores (with ≤ 50% cancer in each); or the patient's doctor discussed active surveillance as a treatment option (as documented in visit notes of the patient's medical record)
boolean
C1318309 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0006826 (UMLS CUI [2,1])
C0439165 (UMLS CUI [2,2])
Able to speak English Language | Able to read English Language | Able to write English Language | Comprehension English Language | Informed Consent | Protocol Compliance
Item
are able to speak, read, write and understand english well enough to provide informed consent and complete study tasks
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0584993 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
C0233733 (UMLS CUI [4,1])
C0376245 (UMLS CUI [4,2])
C0021430 (UMLS CUI [5])
C0525058 (UMLS CUI [6])
Absence Decision Making Treatment
Item
has not made a treatment decision prior to consent, as per self report
boolean
C0332197 (UMLS CUI [1,1])
C0011109 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Partner
Item
for partners/close allies:
boolean
C0682323 (UMLS CUI [1])
Partner Decision Making Treatment
Item
considered a partner/close ally to the patient in the treatment making decision, as reported by the patient
boolean
C0682323 (UMLS CUI [1,1])
C0011109 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
Able to speak English Language | Able to read English Language | Able to write English Language | Comprehension English Language | Informed Consent | Protocol Compliance
Item
are able to speak, read, write and understand english well enough to provide informed consent and complete study tasks
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0584993 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
C0233733 (UMLS CUI [4,1])
C0376245 (UMLS CUI [4,2])
C0021430 (UMLS CUI [5])
C0525058 (UMLS CUI [6])
Age
Item
18 years old or older
boolean
C0001779 (UMLS CUI [1])
Patients
Item
for patients:
boolean
C0030705 (UMLS CUI [1])
Cancer Other | Exception Prostate carcinoma | Exception Skin carcinoma
Item
history of a cancer other than prostate cancer and non-melanoma skin cancer
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0699893 (UMLS CUI [3,2])
Mental disorders Exclude Informed Consent | Impaired cognition Excludes Informed Consent | Mental disorder Study Subject Participation Status Excluded | Impaired cognition Study Subject Participation Status Excluded | Psychiatric symptom Treatment required for
Item
significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent or participating in the study activities (i.e., acute psychiatric symptoms which require individual treatment)
boolean
C0004936 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0338656 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
C0004936 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C0338656 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
C0233401 (UMLS CUI [5,1])
C0332121 (UMLS CUI [5,2])
Partner
Item
for partners/close allies:
boolean
C0682323 (UMLS CUI [1])
Mental disorders Exclude Informed Consent | Impaired cognition Excludes Informed Consent | Mental disorder Study Subject Participation Status Excluded | Impaired cognition Study Subject Participation Status Excluded | Psychiatric symptom Treatment required for
Item
significant psychiatric or cognitive disturbance sufficient, in the investigator's judgment, to preclude providing informed consent or participating in the study activities (i.e., acute psychiatric symptoms which require individual treatment)
boolean
C0004936 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0338656 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
C0004936 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C0332196 (UMLS CUI [3,3])
C0338656 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C0332196 (UMLS CUI [4,3])
C0233401 (UMLS CUI [5,1])
C0332121 (UMLS CUI [5,2])