Age | Postmenopausal state
Item
female, aged 50 years or older, postmenopausal.
boolean
C0001779 (UMLS CUI [1])
C0232970 (UMLS CUI [2])
Invasive carcinoma of breast Estrogen receptor positive TNM Breast tumor staging Immunohistochemistry | Invasive carcinoma of breast Progesterone receptor positive TNM Breast tumor staging Immunohistochemistry | Aromatase Inhibitors Standard Dose Planned
Item
patients with histologically proven stage 0-iii invasive carcinoma of the breast that is estrogen receptor and/or progesterone receptor positive by immunohistochemical staining, who are planning to start treatment with a standard dose of aromatase inhibitor (ai) therapy.
boolean
C0853879 (UMLS CUI [1,1])
C0279754 (UMLS CUI [1,2])
C0474926 (UMLS CUI [1,3])
C0021044 (UMLS CUI [1,4])
C0853879 (UMLS CUI [2,1])
C0279759 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
C0021044 (UMLS CUI [2,4])
C0593802 (UMLS CUI [3,1])
C1442989 (UMLS CUI [3,2])
C0178602 (UMLS CUI [3,3])
C1301732 (UMLS CUI [3,4])
Primary tumor Excision | Indication Primary tumor Excision | Operative Surgical Procedures Additional Absent | Reconstructive Surgical Procedures Absent
Item
subjects must have undergone surgical resection of their primary tumor, as indicated. the most recent surgery must have been performed at least 4 weeks before the baseline evaluation and no additional surgeries (including reconstructive procedures) should be planned during study participation.
boolean
C0677930 (UMLS CUI [1,1])
C0728940 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0677930 (UMLS CUI [2,2])
C0728940 (UMLS CUI [2,3])
C0543467 (UMLS CUI [3,1])
C1524062 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
C0524865 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
Cytotoxic Chemotherapy Completed
Item
cytoxic chemotherapy, if applicable, must have been completed at least 4 weeks before the baseline evaluation.
boolean
C0677881 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Therapeutic radiology procedure Completed
Item
radiation therapy, if applicable, must have been completed at least 2 weeks before baseline evaluation.
boolean
C1522449 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
ECOG performance status
Item
eastern cooperative oncology group performance status 0-2.
boolean
C1520224 (UMLS CUI [1])
Ability operate Accelerometer
Item
ability to operate the accelerometer
boolean
C0085732 (UMLS CUI [1,1])
C3242339 (UMLS CUI [1,2])
C0178951 (UMLS CUI [1,3])
Sleep Apnea | Restless Legs Syndrome
Item
diagnosis of sleep apnea or restless leg syndrome.
boolean
C0037315 (UMLS CUI [1])
C0035258 (UMLS CUI [2])
Wheelchair Usually Used During ambulation
Item
use of a wheelchair for ambulation most of the time.
boolean
C4321408 (UMLS CUI [1,1])
C4302601 (UMLS CUI [1,2])
Shift worker | Sleep Plan Unusual
Item
second or third shift workers or other non-traditional sleep schedules.
boolean
C0425104 (UMLS CUI [1])
C0037313 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C2700116 (UMLS CUI [2,3])
Arthritis Interferes with Evaluation Pain | Arthritis Interferes with Evaluation Activity level | Rheumatoid Arthritis | Lupus Erythematosus, Systemic | Spondylarthropathy | Arthritis, Psoriatic | Polymyalgia Rheumatica | Parkinson Disease | Malignant Neoplasm Involving Bone
Item
history of medical arthritic disease that could confound or interfere with evaluation of pain or activity level, including but not limited to inflammatory arthritis (rheumatoid arthritis, systemic lupus, spondyloarthropathy, psoriatic arthritis, polymyalgia rheumatica), parkinson's disease, and cancer involving the bone.
boolean
C0003864 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1261322 (UMLS CUI [1,3])
C0030193 (UMLS CUI [1,4])
C0003864 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C1261322 (UMLS CUI [2,3])
C0683317 (UMLS CUI [2,4])
C0003873 (UMLS CUI [3])
C0024141 (UMLS CUI [4])
C0949691 (UMLS CUI [5])
C0003872 (UMLS CUI [6])
C0032533 (UMLS CUI [7])
C0030567 (UMLS CUI [8])
C0006826 (UMLS CUI [9,1])
C1314939 (UMLS CUI [9,2])
C0262950 (UMLS CUI [9,3])
Medical condition Serious Hospitalization Required | Medical condition Unstable Hospitalization Required | Medical condition Serious compromises Study Subject Participation Status | Medical condition Unstable compromises Study Subject Participation Status
Item
serious or unstable medical condition that could likely lead to hospitalization during the course of the study or compromise study participation
boolean
C3843040 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C1708385 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C1708385 (UMLS CUI [2,3])
C3843040 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C2945640 (UMLS CUI [3,3])
C2348568 (UMLS CUI [3,4])
C3843040 (UMLS CUI [4,1])
C0443343 (UMLS CUI [4,2])
C2945640 (UMLS CUI [4,3])
C2348568 (UMLS CUI [4,4])