ID

26218

Description

Cognitive Function in Older Women With Stage I, Stage II, or Stage III Breast Cancer Receiving Hormone Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00681928

Link

https://clinicaltrials.gov/show/NCT00681928

Keywords

Versions (1)
  1. 10/11/17 10/11/17 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 11, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00681928

English

Eligibility Breast Cancer NCT00681928

1 forms  
Criteria
Description

Criteria

meets 1 of the following criteria:
Description

Criteria Quantity Fulfill

Data type

boolean

Alias
UMLS CUI [1,1]
C0243161
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C1550543
patient diagnosed with breast cancer
Description

Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0678222
stage i-iii disease
Description

TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1]
C0474926
estrogen receptor- and/or progesterone receptor-positive
Description

Estrogen receptor positive | progesterone receptor positive

Data type

boolean

Alias
UMLS CUI [1]
C0279754
UMLS CUI [2]
C0279759
planning to start treatment with anastrozole or letrozole
Description

Anastrozole Planned | Letrozole Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0290883
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0246421
UMLS CUI [2,2]
C1301732
age-matched healthy volunteer (control)
Description

Healthy Volunteers | Age Matched | Control Group

Data type

boolean

Alias
UMLS CUI [1]
C1708335
UMLS CUI [2,1]
C0001779
UMLS CUI [2,2]
C0150103
UMLS CUI [3]
C0009932
no history of breast cancer
Description

Exclusion Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0678222
not receiving adjuvant aromatase inhibitor therapy
Description

Exclusion Aromatase Inhibitors Adjuvant therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0593802
UMLS CUI [1,3]
C0677850
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
postmenopausal
Description

Postmenopausal state

Data type

boolean

Alias
UMLS CUI [1]
C0232970
able to converse, write, and read english
Description

Able to speak English Language | Able to write English Language | Able to read English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0584993
UMLS CUI [2,2]
C0376245
UMLS CUI [3,1]
C0586740
UMLS CUI [3,2]
C0376245
no claustrophobia (patients participating in the pet scan correlative study)
Description

Exclusion Claustrophobia | Study Subject Participation Status | PET scan Correlative Study

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0008909
UMLS CUI [2]
C2348568
UMLS CUI [3,1]
C0032743
UMLS CUI [3,2]
C1511524
prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Description

ID.14

Data type

boolean

no prior hormonal therapy, including estrogen replacement therapy
Description

Exclusion Hormone Therapy | Exclusion Estrogen Replacement Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0279025
UMLS CUI [2,1]
C2828389
UMLS CUI [2,2]
C0014935
no previous treatment with cns radiation
Description

Exclusion Therapeutic radiology procedure Central Nervous System

Data type

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C1522449
UMLS CUI [1,3]
C3714787
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Similar models

Eligibility Breast Cancer NCT00681928

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Criteria Quantity Fulfill
Item
meets 1 of the following criteria:
boolean
C0243161 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
Breast Carcinoma
Item
patient diagnosed with breast cancer
boolean
C0678222 (UMLS CUI [1])
TNM Breast tumor staging
Item
stage i-iii disease
boolean
C0474926 (UMLS CUI [1])
Estrogen receptor positive | progesterone receptor positive
Item
estrogen receptor- and/or progesterone receptor-positive
boolean
C0279754 (UMLS CUI [1])
C0279759 (UMLS CUI [2])
Anastrozole Planned | Letrozole Planned
Item
planning to start treatment with anastrozole or letrozole
boolean
C0290883 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0246421 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Healthy Volunteers | Age Matched | Control Group
Item
age-matched healthy volunteer (control)
boolean
C1708335 (UMLS CUI [1])
C0001779 (UMLS CUI [2,1])
C0150103 (UMLS CUI [2,2])
C0009932 (UMLS CUI [3])
Exclusion Breast Carcinoma
Item
no history of breast cancer
boolean
C2828389 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Exclusion Aromatase Inhibitors Adjuvant therapy
Item
not receiving adjuvant aromatase inhibitor therapy
boolean
C2828389 (UMLS CUI [1,1])
C0593802 (UMLS CUI [1,2])
C0677850 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Able to speak English Language | Able to write English Language | Able to read English Language
Item
able to converse, write, and read english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0586740 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Exclusion Claustrophobia | Study Subject Participation Status | PET scan Correlative Study
Item
no claustrophobia (patients participating in the pet scan correlative study)
boolean
C2828389 (UMLS CUI [1,1])
C0008909 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])
C0032743 (UMLS CUI [3,1])
C1511524 (UMLS CUI [3,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.14
Item
see disease characteristics
boolean
Exclusion Hormone Therapy | Exclusion Estrogen Replacement Therapy
Item
no prior hormonal therapy, including estrogen replacement therapy
boolean
C2828389 (UMLS CUI [1,1])
C0279025 (UMLS CUI [1,2])
C2828389 (UMLS CUI [2,1])
C0014935 (UMLS CUI [2,2])
Exclusion Therapeutic radiology procedure Central Nervous System
Item
no previous treatment with cns radiation
boolean
C2828389 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
C3714787 (UMLS CUI [1,3])
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