ID

23687

Description

Yoga to Reduce Cancer Fatigue; ODM derived from: https://clinicaltrials.gov/show/NCT00583739

Link

https://clinicaltrials.gov/show/NCT00583739

Keywords

Versions (1)
  1. 7/10/17 7/10/17 -
Uploaded on

July 10, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Neoplasm NCT00583739

English

Eligibility Breast Neoplasm NCT00583739

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
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.
Description

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

Data type

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C0444498
UMLS CUI [3]
C0007124
UMLS CUI [4]
C0279563
UMLS CUI [5]
C0010701
UMLS CUI [6]
C0278601
UMLS CUI [7]
C0853879
UMLS CUI [8,1]
C0678222
UMLS CUI [8,2]
C0474926
treatment completion within the past calendar year.
Description

Treatment completed

Data type

boolean

Alias
UMLS CUI [1]
C0580352
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.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
life expectancy of greater than 1 year.
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
karnofsky ≥ 60%; see appendix a.
Description

Karnofsky Performance Status

Data type

boolean

Alias
UMLS CUI [1]
C0206065
women of childbearing potential are eligible for this study.
Description

Childbearing Potential

Data type

boolean

Alias
UMLS CUI [1]
C3831118
pregnant women are eligible for this study pending a doctor's note.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
the ability to understand and complete the study questionnaires.
Description

Clinical Trial Subject Questionnaire Completion Ability

Data type

boolean

Alias
UMLS CUI [1,1]
C3890411
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0085732
ability to understand and the willingness to sign a written informed consent document.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who have not recovered from adverse events due to agents administered more than 4 weeks earlier.
Description

Adverse event Due to Pharmaceutical Preparations | Patient recovered Lacking

Data type

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0013227
UMLS CUI [2,1]
C1115804
UMLS CUI [2,2]
C0332268
patients with known metastasis.
Description

Neoplasm Metastasis

Data type

boolean

Alias
UMLS CUI [1]
C0027627
patients who are actively participating in a yoga class.
Description

Participation in yoga

Data type

boolean

Alias
UMLS CUI [1]
C0454430
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.
Description

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

Data type

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [2]
C0009450
UMLS CUI [3]
C0742758
UMLS CUI [4]
C0002965
UMLS CUI [5]
C0003811
UMLS CUI [6,1]
C0004936
UMLS CUI [6,2]
C2945640
UMLS CUI [6,3]
C0681850
UMLS CUI [6,4]
C0018684
UMLS CUI [7,1]
C0748872
UMLS CUI [7,2]
C2945640
UMLS CUI [7,3]
C0681850
UMLS CUI [7,4]
C0018684
UMLS CUI [8,1]
C0681850
UMLS CUI [8,2]
C0018684
UMLS CUI [8,3]
C0347984
UMLS CUI [8,4]
C2979879
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Similar models

Eligibility Breast Neoplasm NCT00583739

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
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])
Item Group
C0680251 (UMLS CUI)
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])
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