Breast Carcinoma | Breast Carcinoma In situ | Noninfiltrating Intraductal Carcinoma | Lobular carcinoma in situ of breast | Phyllodes Tumor | Inflammatory Breast Carcinoma | Invasive carcinoma of breast | Breast Carcinoma TNM Breast tumor staging
Item
potential subjects must have had histologically or cytologically confirmed breast cancer. this includes, but is not limited to: breast cancer-in situ; ductal carcinoma in situ; lobular carcinoma in situ; cystosarcoma phyllodes; inflammatory breast carcinoma; invasive breast carcinoma; and breast cancer not otherwise specified; cancer must be stage 0 through stage iii.
boolean
C0678222 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C0444498 (UMLS CUI [2,2])
C0007124 (UMLS CUI [3])
C0279563 (UMLS CUI [4])
C0010701 (UMLS CUI [5])
C0278601 (UMLS CUI [6])
C0853879 (UMLS CUI [7])
C0678222 (UMLS CUI [8,1])
C0474926 (UMLS CUI [8,2])
Treatment completed
Item
treatment completion within the past calendar year.
boolean
C0580352 (UMLS CUI [1])
Age
Item
age ≥ 18 years. while breast cancer can occur in the pediatric population, the pediatric population is best served by trials specifically designed for their age group.
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
life expectancy of greater than 1 year.
boolean
C0023671 (UMLS CUI [1])
Karnofsky Performance Status
Item
karnofsky ≥ 60%; see appendix a.
boolean
C0206065 (UMLS CUI [1])
Childbearing Potential
Item
women of childbearing potential are eligible for this study.
boolean
C3831118 (UMLS CUI [1])
Pregnancy
Item
pregnant women are eligible for this study pending a doctor's note.
boolean
C0032961 (UMLS CUI [1])
Clinical Trial Subject Questionnaire Completion Ability
Item
the ability to understand and complete the study questionnaires.
boolean
C3890411 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Informed Consent
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0021430 (UMLS CUI [1])
Adverse event Due to Pharmaceutical Preparations | Patient recovered Lacking
Item
patients who have not recovered from adverse events due to agents administered more than 4 weeks earlier.
boolean
C0877248 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C1115804 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
Neoplasm Metastasis
Item
patients with known metastasis.
boolean
C0027627 (UMLS CUI [1])
Participation in yoga
Item
patients who are actively participating in a yoga class.
boolean
C0454430 (UMLS CUI [1])
Comorbidity Uncontrolled | Communicable Diseases | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders compromise Study Subject Health | Social situation compromises Study Subject Health | Study Subject Health During Yoga
Item
known uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would compromise subject health during yoga.
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2])
C0742758 (UMLS CUI [3])
C0002965 (UMLS CUI [4])
C0003811 (UMLS CUI [5])
C0004936 (UMLS CUI [6,1])
C2945640 (UMLS CUI [6,2])
C0681850 (UMLS CUI [6,3])
C0018684 (UMLS CUI [6,4])
C0748872 (UMLS CUI [7,1])
C2945640 (UMLS CUI [7,2])
C0681850 (UMLS CUI [7,3])
C0018684 (UMLS CUI [7,4])
C0681850 (UMLS CUI [8,1])
C0018684 (UMLS CUI [8,2])
C0347984 (UMLS CUI [8,3])
C2979879 (UMLS CUI [8,4])