ID

26062

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00548236

Trefwoorden

Versies (1)
  1. 05-10-17 05-10-17 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

5 oktober 2017

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00548236

Engels

Eligibility Breast Cancer NCT00548236

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Breast Carcinoma TNM clinical staging | Colorectal Carcinoma TNM clinical staging

Datatype

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
Beschrijving

Age

Datatype

boolean

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

Adjuvant therapy Completed Malignant Neoplasm

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Able to speak English Language | Able to read English Language

Datatype

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
Beschrijving

Randomization Willing

Datatype

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
Beschrijving

Ability Participation Physical activity Moderate intensity

Datatype

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
Beschrijving

Major surgery Absent

Datatype

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic cancer
Beschrijving

Neoplasm Metastasis

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Hip Replacement Planned | Knee Replacement Planned

Datatype

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
Beschrijving

Participation Recreational activity Moderate intensity Frequency

Datatype

boolean

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

Body mass index

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
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Similar models

Eligibility Breast Cancer NCT00548236

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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