ID

26210

Beschrijving

Aerobic Exercise, Resistance Exercise, or Flexibility and Relaxation Training in Inactive Older Female Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00662103

Link

https://clinicaltrials.gov/show/NCT00662103

Trefwoorden

Versies (2)
  1. 11-10-17 11-10-17 -
  2. 20-09-21 20-09-21 -
Houder van rechten

See clinialtrials.gov

Geüploaded op

11 oktober 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Eligibility Breast Cancer NCT00662103

Engels

Eligibility Breast Cancer NCT00662103

1 Formulieren  
Criteria
Beschrijving

Criteria

diagnosis of breast cancer
Beschrijving

Breast Carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0678222
stage 0-iii disease
Beschrijving

TNM Breast tumor staging

Datatype

boolean

Alias
UMLS CUI [1]
C0474926
completed chemotherapy or radiotherapy > 2 years ago
Beschrijving

Chemotherapy Completed | Therapeutic radiology procedure Completed

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C0205197
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)
Beschrijving

Exclusion Criteria | Participation Aerobic Exercise Moderate | Jogging | Swimming | Participation Resistive exercise Moderate | Aerobic Exercise Vigorous | Resistive exercise Vigorous

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C0001701
UMLS CUI [2,3]
C0205081
UMLS CUI [3]
C0022400
UMLS CUI [4]
C0039003
UMLS CUI [5,1]
C0679823
UMLS CUI [5,2]
C0203991
UMLS CUI [5,3]
C0205081
UMLS CUI [6,1]
C0001701
UMLS CUI [6,2]
C3841230
UMLS CUI [7,1]
C0203991
UMLS CUI [7,2]
C3841230
no stage iv breast cancer
Beschrijving

Secondary malignant neoplasm of female breast Excluded

Datatype

boolean

Alias
UMLS CUI [1,1]
C0346993
UMLS CUI [1,2]
C2828389
hormone receptor status not specified
Beschrijving

Hormone Receptor Status Unspecified

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Beschrijving

Client Characteristics

Datatype

boolean

Alias
UMLS CUI [1]
C0815172
menopausal status not specified
Beschrijving

Menopausal Status Unspecified

Datatype

boolean

Alias
UMLS CUI [1,1]
C1513126
UMLS CUI [1,2]
C0205370
has obtained medical clearance to participate in study exercise programs
Beschrijving

Participation Clinical Trial Exercise Programs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0015259
UMLS CUI [1,4]
C3484370
no cognitive difficulties that would preclude answering the survey questions, participating in the performance tests, or giving informed consent
Beschrijving

Exclusion Criteria | Impaired cognition Protocol Compliance Unable | Impaired cognition Informed Consent Unable

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0338656
UMLS CUI [2,2]
C0525058
UMLS CUI [2,3]
C1299582
UMLS CUI [3,1]
C0338656
UMLS CUI [3,2]
C0021430
UMLS CUI [3,3]
C1299582
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
Beschrijving

Exclusion Criteria | Medical condition Preventing Exercise Training Moderate | Nervous system disorder Preventing Exercise Training Moderate

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C4279936
UMLS CUI [2,4]
C0205081
UMLS CUI [3,1]
C0027765
UMLS CUI [3,2]
C1292733
UMLS CUI [3,3]
C4279936
UMLS CUI [3,4]
C0205081
prior concurrent therapy:
Beschrijving

Therapeutic procedure

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Beschrijving

ID.13

Datatype

boolean

no concurrent medication that would contraindicate participation in moderate intensity exercise training, as determined by physician clearance and the principal investigator
Beschrijving

Exclusion Criteria | Pharmaceutical Preparations Preventing Exercise Training Moderate

Datatype

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C1292733
UMLS CUI [2,3]
C4279936
UMLS CUI [2,4]
C0205081
concurrent hormonal therapy (e.g., selective estrogen receptor modulator (serm) or aromatase inhibitor) for breast cancer allowed
Beschrijving

Hormone Therapy Breast Carcinoma | Selective Estrogen Receptor Modulators | Aromatase Inhibitors

Datatype

boolean

Alias
UMLS CUI [1,1]
C0279025
UMLS CUI [1,2]
C0678222
UMLS CUI [2]
C0732611
UMLS CUI [3]
C0593802
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Similar models

Eligibility Breast Cancer NCT00662103

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
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])
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])
Secondary malignant neoplasm of female breast Excluded
Item
no stage iv breast cancer
boolean
C0346993 (UMLS CUI [1,1])
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])
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])
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])
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])
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])
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])
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])
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