ID

20109

Description

Diet and Exercise or Normal Care in Overweight or Obese Women Who Have Undergone Treatment for Stage I, Stage II, or Stage III Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00689975

Lien

https://clinicaltrials.gov/show/NCT00689975

Mots-clés

  1. 06/02/2017 06/02/2017 -
Téléchargé le

6 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Breast Cancer NCT00689975

Eligibility Breast Cancer NCT00689975

Criteria
Description

Criteria

diagnosis of stage i, ii, or iii breast cancer
Description

Breast Cancer Stage

Type de données

boolean

Alias
UMLS CUI [1]
C2216702
no metastatic breast cancer
Description

Metastatic breast cancer

Type de données

boolean

Alias
UMLS CUI [1]
C0278488
no inoperable or active loco-regional disease
Description

Inoperable or active loco-regional disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0205187
UMLS CUI [2]
C0277565
body mass index (bmi) > 25
Description

BMI

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
patients must have completed treatment for breast cancer within the past 3-18 months
Description

Completed treatment for breast cancer

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0678222
UMLS CUI [1,3]
C0205197
hormone receptor status not specified
Description

hormone receptor status

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
patient characteristics:
Description

Patient characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
menopausal status not specified
Description

Menopausal status

Type de données

boolean

Alias
UMLS CUI [1]
C0455962
willing and able to attend supervised exercise sessions at least 3 times per week for a period of 24 weeks
Description

Willing to participate

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
patients must be an exercise pre-contemplator, contemplator, or preparer as defined by the transtheoretical model
Description

Transtheoretical model

Type de données

boolean

Alias
UMLS CUI [1]
C3714361
no physical/psychiatric impairment that would seriously impair physical mobility
Description

Physical/psychiatric impairment

Type de données

boolean

Alias
UMLS CUI [1]
C0231171
UMLS CUI [2]
C0004936
no severe nausea, anorexia, or other diseases affecting health (e.g., arthritis and multiple sclerosis)
Description

Comorbidity

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
more than 3 months since prior exercise and not currently engaged in exercise (two or more times per week for at least 30 minutes per session)
Description

Exercise

Type de données

boolean

Alias
UMLS CUI [1]
C0015259
prior concurrent therapy:
Description

Prior concurrent therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0009429
see disease characteristics
Description

Disease characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C1705348
concurrent tamoxifen, other endocrine treatments, and trastuzumab (herceptin®) allowed
Description

Endocrine treatments

Type de données

boolean

Alias
UMLS CUI [1]
C0279025
no concurrent alternative/complementary diets
Description

Diet

Type de données

boolean

Alias
UMLS CUI [1]
C0012155
no concurrent high-dose antioxidant supplement therapy
Description

High-dose antioxidant supplement

Type de données

boolean

Alias
UMLS CUI [1,1]
C0003402
UMLS CUI [1,2]
C0444956
more than 4 months since prior and no concurrent hormone-replacement therapy or oral contraceptives
Description

Hormone-replacement therapy or oral contraceptives

Type de données

boolean

Alias
UMLS CUI [1]
C0282402
UMLS CUI [2]
C0009905

Similar models

Eligibility Breast Cancer NCT00689975

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Breast Cancer Stage
Item
diagnosis of stage i, ii, or iii breast cancer
boolean
C2216702 (UMLS CUI [1])
Metastatic breast cancer
Item
no metastatic breast cancer
boolean
C0278488 (UMLS CUI [1])
Inoperable or active loco-regional disease
Item
no inoperable or active loco-regional disease
boolean
C0006826 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
C0277565 (UMLS CUI [2])
BMI
Item
body mass index (bmi) > 25
boolean
C1305855 (UMLS CUI [1])
Completed treatment for breast cancer
Item
patients must have completed treatment for breast cancer within the past 3-18 months
boolean
C0087111 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
hormone receptor status
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Patient characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Menopausal status
Item
menopausal status not specified
boolean
C0455962 (UMLS CUI [1])
Willing to participate
Item
willing and able to attend supervised exercise sessions at least 3 times per week for a period of 24 weeks
boolean
C0021430 (UMLS CUI [1])
Transtheoretical model
Item
patients must be an exercise pre-contemplator, contemplator, or preparer as defined by the transtheoretical model
boolean
C3714361 (UMLS CUI [1])
Physical/psychiatric impairment
Item
no physical/psychiatric impairment that would seriously impair physical mobility
boolean
C0231171 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Comorbidity
Item
no severe nausea, anorexia, or other diseases affecting health (e.g., arthritis and multiple sclerosis)
boolean
C0009488 (UMLS CUI [1])
Exercise
Item
more than 3 months since prior exercise and not currently engaged in exercise (two or more times per week for at least 30 minutes per session)
boolean
C0015259 (UMLS CUI [1])
Prior concurrent therapy
Item
prior concurrent therapy:
boolean
C0009429 (UMLS CUI [1])
Disease characteristics
Item
see disease characteristics
boolean
C1705348 (UMLS CUI [1])
Endocrine treatments
Item
concurrent tamoxifen, other endocrine treatments, and trastuzumab (herceptin®) allowed
boolean
C0279025 (UMLS CUI [1])
Diet
Item
no concurrent alternative/complementary diets
boolean
C0012155 (UMLS CUI [1])
High-dose antioxidant supplement
Item
no concurrent high-dose antioxidant supplement therapy
boolean
C0003402 (UMLS CUI [1,1])
C0444956 (UMLS CUI [1,2])
Hormone-replacement therapy or oral contraceptives
Item
more than 4 months since prior and no concurrent hormone-replacement therapy or oral contraceptives
boolean
C0282402 (UMLS CUI [1])
C0009905 (UMLS CUI [2])

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