ID

13883

Beschreibung

Exercise Program for Early Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT01140282

Link

https://clinicaltrials.gov/show/NCT01140282

Stichworte

  1. 13.03.16 13.03.16 -
Hochgeladen am

13. März 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Stage I Breast Cancer NCT01140282

Eligibility Stage I Breast Cancer NCT01140282

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
newly diagnosed (i-iii) with a first primary invasive breast cancer
Beschreibung

invasive breast cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0853879
have undergone a lumpectomy or mastectomy
Beschreibung

lumpectomy; mastectomy

Datentyp

boolean

Alias
UMLS CUI [1]
C0851238
UMLS CUI [2]
C0024881
have completed neoadjuvant/adjuvant chemotherapy and able to initiate exercise program (if randomized to that arm) within 12 weeks of therapy completion
Beschreibung

neoadjuvant chemotherapy; adjuvant chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472
UMLS CUI [2]
C0085533
body mass index (bmi) > 25 kg/m^2 or body fat > 30% (determined by dr. dieli-conwright at baseline visit)
Beschreibung

body mass index; body fat

Datentyp

boolean

Alias
UMLS CUI [1]
C0005893
UMLS CUI [2]
C0015665
currently participate in less than 60 minutes of physical activity per week may use adjuvant endocrine therapy if use will be continued for duration of study period
Beschreibung

physical activity; adjuvant endocrine therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C0026606
UMLS CUI [2]
C0281266
nonsmokers (i.e., not smoking during previous 12 months)
Beschreibung

nonsmokers

Datentyp

boolean

Alias
UMLS CUI [1]
C0337672
willing to travel to the exercise facility and usc
Beschreibung

compliance

Datentyp

boolean

Alias
UMLS CUI [1]
C1321605
able to provide physician clearance to participate in exercise program
Beschreibung

exercise program

Datentyp

boolean

Alias
UMLS CUI [1]
C1820660
women of all racial and ethnic backgrounds will be included in the study enrollment process
Beschreibung

ethnicity

Datentyp

boolean

Alias
UMLS CUI [1]
C0015031
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of chronic disease including diabetes, uncontrolled hypertension or thyroid disease
Beschreibung

diabetes; uncontrolled hypertension; thyroid disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0011847
UMLS CUI [2]
C1868885
UMLS CUI [3]
C0040128
weight reduction >= 10% within past 6 months
Beschreibung

weight reduction

Datentyp

boolean

Alias
UMLS CUI [1]
C0311130
diagnosed with human epidermal growth factor receptor 2 (her2)-positive tumor (exclusion due to patient use of herceptin medication for 1 year following chemotherapy)
Beschreibung

HER2-positive carcinoma of breast

Datentyp

boolean

Alias
UMLS CUI [1]
C1960398
metastatic disease
Beschreibung

metastatic disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0027627
planned reconstructive surgery with flap repair during trial and follow-up period
Beschreibung

reconstructive surgery

Datentyp

boolean

Alias
UMLS CUI [1]
C0524865
cardiovascular, respiratory or musculoskeletal disease or joint problems that preclude moderate physical activity
Beschreibung

cardiovascular disease; respiratory disease; musculoskeletal disease; joint problems

Datentyp

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0035204
UMLS CUI [3]
C0026857
UMLS CUI [4]
C0575044

Ähnliche Modelle

Eligibility Stage I Breast Cancer NCT01140282

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
invasive breast cancer
Item
newly diagnosed (i-iii) with a first primary invasive breast cancer
boolean
C0853879 (UMLS CUI [1])
lumpectomy; mastectomy
Item
have undergone a lumpectomy or mastectomy
boolean
C0851238 (UMLS CUI [1])
C0024881 (UMLS CUI [2])
neoadjuvant chemotherapy; adjuvant chemotherapy
Item
have completed neoadjuvant/adjuvant chemotherapy and able to initiate exercise program (if randomized to that arm) within 12 weeks of therapy completion
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2])
body mass index; body fat
Item
body mass index (bmi) > 25 kg/m^2 or body fat > 30% (determined by dr. dieli-conwright at baseline visit)
boolean
C0005893 (UMLS CUI [1])
C0015665 (UMLS CUI [2])
physical activity; adjuvant endocrine therapy
Item
currently participate in less than 60 minutes of physical activity per week may use adjuvant endocrine therapy if use will be continued for duration of study period
boolean
C0026606 (UMLS CUI [1])
C0281266 (UMLS CUI [2])
nonsmokers
Item
nonsmokers (i.e., not smoking during previous 12 months)
boolean
C0337672 (UMLS CUI [1])
compliance
Item
willing to travel to the exercise facility and usc
boolean
C1321605 (UMLS CUI [1])
exercise program
Item
able to provide physician clearance to participate in exercise program
boolean
C1820660 (UMLS CUI [1])
ethnicity
Item
women of all racial and ethnic backgrounds will be included in the study enrollment process
boolean
C0015031 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
diabetes; uncontrolled hypertension; thyroid disease
Item
history of chronic disease including diabetes, uncontrolled hypertension or thyroid disease
boolean
C0011847 (UMLS CUI [1])
C1868885 (UMLS CUI [2])
C0040128 (UMLS CUI [3])
weight reduction
Item
weight reduction >= 10% within past 6 months
boolean
C0311130 (UMLS CUI [1])
HER2-positive carcinoma of breast
Item
diagnosed with human epidermal growth factor receptor 2 (her2)-positive tumor (exclusion due to patient use of herceptin medication for 1 year following chemotherapy)
boolean
C1960398 (UMLS CUI [1])
metastatic disease
Item
metastatic disease
boolean
C0027627 (UMLS CUI [1])
reconstructive surgery
Item
planned reconstructive surgery with flap repair during trial and follow-up period
boolean
C0524865 (UMLS CUI [1])
cardiovascular disease; respiratory disease; musculoskeletal disease; joint problems
Item
cardiovascular, respiratory or musculoskeletal disease or joint problems that preclude moderate physical activity
boolean
C0007222 (UMLS CUI [1])
C0035204 (UMLS CUI [2])
C0026857 (UMLS CUI [3])
C0575044 (UMLS CUI [4])

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