Gender | Breast Carcinoma | Age | Noninfiltrating Intraductal Carcinoma | Breast Carcinoma TNM Breast tumor staging | Chemotherapy Absent | Therapeutic radiology procedure Absent | Therapeutic procedure Long-term | Aromatase Inhibitors | Estrogen Receptor Modulators | Cardiovascular Disease
Item
female breast cancer patients between the ages of 18 and 70 years of age with a diagnosis of ductal carcinoma in situ (dcis) or stage i, ii, or iiia breast cancer and who are not currently receiving (and do not plan to receive during the duration of the study) chemotherapy or radiation therapy. the participant may be taking longer term therapies such as aromatase inhibitors, estrogen receptor modulators, etc. the upper age limit of 70 years was chosen to reduce the likelihood of adverse events or study drop-out due to increasing comorbidities (e.g., cardiovascular disease) that occur with age.
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0007124 (UMLS CUI [4])
C0678222 (UMLS CUI [5,1])
C0474926 (UMLS CUI [5,2])
C0392920 (UMLS CUI [6,1])
C0332197 (UMLS CUI [6,2])
C1522449 (UMLS CUI [7,1])
C0332197 (UMLS CUI [7,2])
C0087111 (UMLS CUI [8,1])
C0443252 (UMLS CUI [8,2])
C0593802 (UMLS CUI [9])
C0752229 (UMLS CUI [10])
C0007222 (UMLS CUI [11])
Operative Surgical Procedures | Enrollment Delayed
Item
if the patient has undergone a surgical procedure, enrollment will be delayed until ≥
boolean
C0543467 (UMLS CUI [1])
C1516879 (UMLS CUI [2,1])
C0205421 (UMLS CUI [2,2])
Enrollment Post Procedure
Item
8 weeks post-procedure.
boolean
C1516879 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
Able to speak English Language
Item
english speaking.
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
Study Subject Participation Status Approved Primary Care Physician | Study Subject Participation Status Approved Oncologist
Item
medical clearance for participation provided by primary care physician or oncologist.
boolean
C2348568 (UMLS CUI [1,1])
C0205540 (UMLS CUI [1,2])
C0033131 (UMLS CUI [1,3])
C2348568 (UMLS CUI [2,1])
C0205540 (UMLS CUI [2,2])
C0259990 (UMLS CUI [2,3])
Moderate physical activity minutes per week | Vigorous physical activity minutes per week
Item
participating, on average, in no more than 60 minutes of moderate physical activity or no more than 30 minutes of vigorous activity per week during the past six months.
boolean
C4482418 (UMLS CUI [1,1])
C0556975 (UMLS CUI [1,2])
C4267713 (UMLS CUI [2,1])
C0556975 (UMLS CUI [2,2])
Dementia | Organic brain syndrome
Item
diagnosis of dementia or organic brain syndrome.
boolean
C0497327 (UMLS CUI [1])
C0029221 (UMLS CUI [2])
Characteristics Medical Interfere with Study Protocol | Characteristics Psychological Interfere with Study Protocol | Characteristics social Interfere with Study Protocol | Psychotic Disorders | Schizophrenia
Item
medical, psychological, or social characteristic that would interfere with ability to fully participate in program activities and assessments (e.g., psychosis, schizophrenia, etc.).
boolean
C1521970 (UMLS CUI [1,1])
C0205476 (UMLS CUI [1,2])
C0521102 (UMLS CUI [1,3])
C2348563 (UMLS CUI [1,4])
C1521970 (UMLS CUI [2,1])
C0205486 (UMLS CUI [2,2])
C0521102 (UMLS CUI [2,3])
C2348563 (UMLS CUI [2,4])
C1521970 (UMLS CUI [3,1])
C0728831 (UMLS CUI [3,2])
C0521102 (UMLS CUI [3,3])
C2348563 (UMLS CUI [3,4])
C0033975 (UMLS CUI [4])
C0036341 (UMLS CUI [5])
Medical contraindication Physical activity Regular
Item
contraindication to participation in a regular physical activity program.
boolean
C1301624 (UMLS CUI [1,1])
C0026606 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
Neoplasm Metastasis | Recurrent disease
Item
metastatic or recurrent disease.
boolean
C0027627 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
Lacking Able to walk
Item
inability to ambulate.
boolean
C0332268 (UMLS CUI [1,1])
C2712089 (UMLS CUI [1,2])
Elective Surgical Procedure Interferes with Intervention | Reconstructive breast surgery
Item
anticipates undergoing elective surgery during the duration of the intervention which would interfere with intervention participation (e.g., breast reconstructive surgery).
boolean
C0206058 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C1408823 (UMLS CUI [2])
Travel Interferes with Study Protocol
Item
planned travel that would interfere with scheduled study sessions (no travel in the 1st 4 months and no travel ≥ 1 week in the last 8 weeks of the intervention).
boolean
C0040802 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])