Gender | Breast Carcinoma | Neoplasm Metastasis Absent | Recommendation Chemotherapy
Item
1. women or men with histologically confirmed breast cancer and no evidence of metastatic disease with a recommendation to begin chemotherapy within 4 weeks.
boolean
C0079399 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
C0027627 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0034866 (UMLS CUI [4,1])
C0392920 (UMLS CUI [4,2])
Prior surgery Patient recovered
Item
2. patients must have recovered from prior surgery.
boolean
C0455610 (UMLS CUI [1,1])
C1115804 (UMLS CUI [1,2])
Able to walk Without Help | Able to walk Without Oxygen support
Item
3. patients must be able to walk unassisted without oxygen
boolean
C2712089 (UMLS CUI [1,1])
C3827452 (UMLS CUI [1,2])
C2712089 (UMLS CUI [2,1])
C0332288 (UMLS CUI [2,2])
C3872899 (UMLS CUI [2,3])
Physical activity questionnaire Completion | Age
Item
4. patients must complete the physical activity readiness questionnaire with "no" answers to all questions; if patient responds with yes answers, or is over age 69, approval must be obtained from the patient's primary care physician or treating medical oncologist to participate in the study.
boolean
C4264334 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Fasting Duration Able | Hematologic Test | Measurement of basal metabolic rate
Item
5. able to fast for 12 hours for blood work and basal metabolic rate measurement.
boolean
C0015663 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0018941 (UMLS CUI [2])
C0542499 (UMLS CUI [3])
Karnofsky Performance Status
Item
6. karnofsky performance status > or = to 80%.
boolean
C0206065 (UMLS CUI [1])
Physical therapy
Item
7. previous or ongoing physical therapy treatments are acceptable.
boolean
C0949766 (UMLS CUI [1])
Study Subject Participation Status | Therapies, Investigational | Weight loss Clinical Trial Absent
Item
8. participants may be enrolled on other treatment-based clinical trials but may not be enrolled on any other weight loss trials.
boolean
C2348568 (UMLS CUI [1])
C0949266 (UMLS CUI [2])
C1262477 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C0332197 (UMLS CUI [3,3])
Moderate physical activity minutes per week | Vigorous physical activity minutes per week | Leisure Time Exercise Questionnaires
Item
9. participants must have a baseline activity level of < 150 minutes/wk of moderate to vigorous activity as calculated using the moderate to vigorous components of the lteq (leisure time exercise questionnaire) for physical activity (completed during screening).
boolean
C4482418 (UMLS CUI [1,1])
C0556975 (UMLS CUI [1,2])
C4267713 (UMLS CUI [2,1])
C0556975 (UMLS CUI [2,2])
C0086542 (UMLS CUI [3,1])
C0015259 (UMLS CUI [3,2])
C0034394 (UMLS CUI [3,3])
Age
Item
1. patients less than 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Acute myocardial infarction | Cerebrovascular accident Recent
Item
2. patients with history of acute mi (myocardial infarction) or cva (cerebral vascular accident) within the last 12 months.
boolean
C0155626 (UMLS CUI [1])
C0038454 (UMLS CUI [2,1])
C0332185 (UMLS CUI [2,2])
Patient dependence on Oxygen support
Item
3. patients who are oxygen dependent.
boolean
C0439857 (UMLS CUI [1,1])
C3872899 (UMLS CUI [1,2])
Informed Consent Unable
Item
4. patients unable to give informed consent indicating they are aware of the investigational nature of this intervention prior to entry into the study.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Karnofsky Performance Status
Item
5. patients with a karnofsky performance status of < 80%.
boolean
C0206065 (UMLS CUI [1])
Pregnancy
Item
6. pregnant.
boolean
C0032961 (UMLS CUI [1])
Lacking Able to read English Language | Lacking Able to write English Language
Item
7. unable to read or write in english.
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0584993 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])