ID

26062

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT00548236

Stichworte

Versionen (1)
  1. 05.10.17 05.10.17 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

5. Oktober 2017

DOI

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Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00548236

Englisch

Eligibility Breast Cancer NCT00548236

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

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

Breast Carcinoma TNM clinical staging | Colorectal Carcinoma TNM clinical staging

Datentyp

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
Beschreibung

Age

Datentyp

boolean

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

Adjuvant therapy Completed Malignant Neoplasm

Datentyp

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
Beschreibung

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

Datentyp

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
Beschreibung

Able to speak English Language | Able to read English Language

Datentyp

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
Beschreibung

Randomization Willing

Datentyp

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
Beschreibung

Ability Participation Physical activity Moderate intensity

Datentyp

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
Beschreibung

Major surgery Absent

Datentyp

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic cancer
Beschreibung

Neoplasm Metastasis

Datentyp

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
Beschreibung

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

Datentyp

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
Beschreibung

Hip Replacement Planned | Knee Replacement Planned

Datentyp

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
Beschreibung

Participation Recreational activity Moderate intensity Frequency

Datentyp

boolean

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

Body mass index

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
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Ähnliche Modelle

Eligibility Breast Cancer NCT00548236

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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