ID

26062

Descrizione

The Active After Cancer Trial (AACT); ODM derived from: https://clinicaltrials.gov/show/NCT00548236

collegamento

https://clinicaltrials.gov/show/NCT00548236

Keywords

versioni (1)
  1. 05/10/17 05/10/17 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

5 ottobre 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00548236

Inglese

Eligibility Breast Cancer NCT00548236

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed stage i-iii breast or colorectal cancer
Descrizione

Breast Carcinoma TNM clinical staging | Colorectal Carcinoma TNM clinical staging

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C3258246
UMLS CUI [2,1]
C0009402
UMLS CUI [2,2]
C3258246
18 years of age or older
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
completed adjuvant treatment(for current malignancy)
Descrizione

Adjuvant therapy Completed Malignant Neoplasm

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0677850
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C0006826
completion of all adjuvant chemotherapy and radiation (with the exception of adjuvant herceptin and/or tamoxifen/aromatase inhibitor therapy for breast cancer patients) between 2 and 36 months prior to enrollment
Descrizione

Adjuvant Chemotherapy Completed | Therapeutic radiology procedure Completed | Exception Herceptin Breast Carcinoma | Exception Tamoxifen Breast Carcinoma | Exception Aromatase Inhibitors Breast Carcinoma

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C0205197
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0338204
UMLS CUI [3,3]
C0678222
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0039286
UMLS CUI [4,3]
C0678222
UMLS CUI [5,1]
C1705847
UMLS CUI [5,2]
C0593802
UMLS CUI [5,3]
C0678222
ability to speak and read english
Descrizione

Able to speak English Language | Able to read English Language

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0586740
UMLS CUI [2,2]
C0376245
willingness to be randomized
Descrizione

Randomization Willing

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0600109
medical clearance from an oncologist or primary care physician stating the participant is able to participate in an unsupervised, moderate-intensity physical activity program
Descrizione

Ability Participation Physical activity Moderate intensity

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0026606
UMLS CUI [1,4]
C4081855
no major surgery within 2 months of study enrollment or planned during study period
Descrizione

Major surgery Absent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0679637
UMLS CUI [1,2]
C0332197
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic cancer
Descrizione

Neoplasm Metastasis

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0027627
uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness that would limit compliance with study requirements
Descrizione

Comorbidity Uncontrolled | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders Compliance behavior Limited

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205318
UMLS CUI [2]
C0742758
UMLS CUI [3]
C0002965
UMLS CUI [4]
C0003811
UMLS CUI [5,1]
C0004936
UMLS CUI [5,2]
C1321605
UMLS CUI [5,3]
C0439801
plans to have hip or knee replacement within a year
Descrizione

Hip Replacement Planned | Knee Replacement Planned

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392806
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0086511
UMLS CUI [2,2]
C1301732
participation in more than 60 minutes a week of moderate-intensity recreational activity as assessed by the international physical activity questionnaire short form
Descrizione

Participation Recreational activity Moderate intensity Frequency

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0034872
UMLS CUI [1,3]
C4081855
UMLS CUI [1,4]
C0439603
bmi >47
Descrizione

Body mass index

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1305855
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Similar models

Eligibility Breast Cancer NCT00548236

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma TNM clinical staging | Colorectal Carcinoma TNM clinical staging
Item
histologically confirmed stage i-iii breast or colorectal cancer
boolean
C0678222 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C0009402 (UMLS CUI [2,1])
C3258246 (UMLS CUI [2,2])
Age
Item
18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Adjuvant therapy Completed Malignant Neoplasm
Item
completed adjuvant treatment(for current malignancy)
boolean
C0677850 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
Adjuvant Chemotherapy Completed | Therapeutic radiology procedure Completed | Exception Herceptin Breast Carcinoma | Exception Tamoxifen Breast Carcinoma | Exception Aromatase Inhibitors Breast Carcinoma
Item
completion of all adjuvant chemotherapy and radiation (with the exception of adjuvant herceptin and/or tamoxifen/aromatase inhibitor therapy for breast cancer patients) between 2 and 36 months prior to enrollment
boolean
C0085533 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0338204 (UMLS CUI [3,2])
C0678222 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0039286 (UMLS CUI [4,2])
C0678222 (UMLS CUI [4,3])
C1705847 (UMLS CUI [5,1])
C0593802 (UMLS CUI [5,2])
C0678222 (UMLS CUI [5,3])
Able to speak English Language | Able to read English Language
Item
ability to speak and read english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Randomization Willing
Item
willingness to be randomized
boolean
C0034656 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Ability Participation Physical activity Moderate intensity
Item
medical clearance from an oncologist or primary care physician stating the participant is able to participate in an unsupervised, moderate-intensity physical activity program
boolean
C0085732 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0026606 (UMLS CUI [1,3])
C4081855 (UMLS CUI [1,4])
Major surgery Absent
Item
no major surgery within 2 months of study enrollment or planned during study period
boolean
C0679637 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis
Item
metastatic cancer
boolean
C0027627 (UMLS CUI [1])
Comorbidity Uncontrolled | Symptomatic congestive heart failure | Angina, Unstable | Cardiac Arrhythmia | Mental disorders Compliance behavior Limited
Item
uncontrolled intercurrent illness including, but not limited to, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness that would limit compliance with study requirements
boolean
C0009488 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0742758 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0003811 (UMLS CUI [4])
C0004936 (UMLS CUI [5,1])
C1321605 (UMLS CUI [5,2])
C0439801 (UMLS CUI [5,3])
Hip Replacement Planned | Knee Replacement Planned
Item
plans to have hip or knee replacement within a year
boolean
C0392806 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0086511 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Participation Recreational activity Moderate intensity Frequency
Item
participation in more than 60 minutes a week of moderate-intensity recreational activity as assessed by the international physical activity questionnaire short form
boolean
C0679823 (UMLS CUI [1,1])
C0034872 (UMLS CUI [1,2])
C4081855 (UMLS CUI [1,3])
C0439603 (UMLS CUI [1,4])
Body mass index
Item
bmi >47
boolean
C1305855 (UMLS CUI [1])
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