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Information:
Fel:
ID
26210
Beskrivning
Aerobic Exercise, Resistance Exercise, or Flexibility and Relaxation Training in Inactive Older Female Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00662103
Länk
https://clinicaltrials.gov/show/NCT00662103
Nyckelord
Versioner (2)
- 2017-10-11 2017-10-11 -
- 2021-09-20 2021-09-20 -
Rättsinnehavare
See clinialtrials.gov
Uppladdad den
11 oktober 2017
DOI
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Licens
Creative Commons BY-NC 3.0
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Eligibility Breast Cancer NCT00662103
Eligibility Breast Cancer NCT00662103
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00662103
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Breast Carcinoma
Item
diagnosis of breast cancer
boolean
C0678222 (UMLS CUI [1])
TNM Breast tumor staging
Item
stage 0-iii disease
boolean
C0474926 (UMLS CUI [1])
Chemotherapy Completed | Therapeutic radiology procedure Completed
Item
completed chemotherapy or radiotherapy > 2 years ago
boolean
C0392920 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0205197 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
Exclusion Criteria | Participation Aerobic Exercise Moderate | Jogging | Swimming | Participation Resistive exercise Moderate | Aerobic Exercise Vigorous | Resistive exercise Vigorous
Item
is not a regular participant in moderate aerobic exercise (i.e., jogging, swimming) or moderate resistance exercise (> 3 times/week for ≥ 30 minutes/session) or in vigorous aerobic or resistance exercise (> 3 times/week for ≥ 20 minutes/session)
boolean
C0680251 (UMLS CUI [1])
C0679823 (UMLS CUI [2,1])
C0001701 (UMLS CUI [2,2])
C0205081 (UMLS CUI [2,3])
C0022400 (UMLS CUI [3])
C0039003 (UMLS CUI [4])
C0679823 (UMLS CUI [5,1])
C0203991 (UMLS CUI [5,2])
C0205081 (UMLS CUI [5,3])
C0001701 (UMLS CUI [6,1])
C3841230 (UMLS CUI [6,2])
C0203991 (UMLS CUI [7,1])
C3841230 (UMLS CUI [7,2])
C0679823 (UMLS CUI [2,1])
C0001701 (UMLS CUI [2,2])
C0205081 (UMLS CUI [2,3])
C0022400 (UMLS CUI [3])
C0039003 (UMLS CUI [4])
C0679823 (UMLS CUI [5,1])
C0203991 (UMLS CUI [5,2])
C0205081 (UMLS CUI [5,3])
C0001701 (UMLS CUI [6,1])
C3841230 (UMLS CUI [6,2])
C0203991 (UMLS CUI [7,1])
C3841230 (UMLS CUI [7,2])
Secondary malignant neoplasm of female breast Excluded
Item
no stage iv breast cancer
boolean
C0346993 (UMLS CUI [1,1])
C2828389 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,2])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C1513126 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Participation Clinical Trial Exercise Programs
Item
has obtained medical clearance to participate in study exercise programs
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C3484370 (UMLS CUI [1,4])
C0008976 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C3484370 (UMLS CUI [1,4])
Exclusion Criteria | Impaired cognition Protocol Compliance Unable | Impaired cognition Informed Consent Unable
Item
no cognitive difficulties that would preclude answering the survey questions, participating in the performance tests, or giving informed consent
boolean
C0680251 (UMLS CUI [1])
C0338656 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0338656 (UMLS CUI [3,1])
C0021430 (UMLS CUI [3,2])
C1299582 (UMLS CUI [3,3])
C0338656 (UMLS CUI [2,1])
C0525058 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0338656 (UMLS CUI [3,1])
C0021430 (UMLS CUI [3,2])
C1299582 (UMLS CUI [3,3])
Exclusion Criteria | Medical condition Preventing Exercise Training Moderate | Nervous system disorder Preventing Exercise Training Moderate
Item
no medical condition or movement or neurological disorder that would contraindicate participation in moderate intensity exercise training, as determined by physician clearance and the principal investigator
boolean
C0680251 (UMLS CUI [1])
C3843040 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C4279936 (UMLS CUI [2,3])
C0205081 (UMLS CUI [2,4])
C0027765 (UMLS CUI [3,1])
C1292733 (UMLS CUI [3,2])
C4279936 (UMLS CUI [3,3])
C0205081 (UMLS CUI [3,4])
C3843040 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C4279936 (UMLS CUI [2,3])
C0205081 (UMLS CUI [2,4])
C0027765 (UMLS CUI [3,1])
C1292733 (UMLS CUI [3,2])
C4279936 (UMLS CUI [3,3])
C0205081 (UMLS CUI [3,4])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.13
Item
see disease characteristics
boolean
Exclusion Criteria | Pharmaceutical Preparations Preventing Exercise Training Moderate
Item
no concurrent medication that would contraindicate participation in moderate intensity exercise training, as determined by physician clearance and the principal investigator
boolean
C0680251 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C4279936 (UMLS CUI [2,3])
C0205081 (UMLS CUI [2,4])
C0013227 (UMLS CUI [2,1])
C1292733 (UMLS CUI [2,2])
C4279936 (UMLS CUI [2,3])
C0205081 (UMLS CUI [2,4])
Hormone Therapy Breast Carcinoma | Selective Estrogen Receptor Modulators | Aromatase Inhibitors
Item
concurrent hormonal therapy (e.g., selective estrogen receptor modulator (serm) or aromatase inhibitor) for breast cancer allowed
boolean
C0279025 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0732611 (UMLS CUI [2])
C0593802 (UMLS CUI [3])
C0678222 (UMLS CUI [1,2])
C0732611 (UMLS CUI [2])
C0593802 (UMLS CUI [3])