ID

19575

Description

Quality of Life in Female Breast Cancer Survivors and Their Spouse, Partner, or Acquaintance; ODM derived from: https://clinicaltrials.gov/show/NCT00309933

Link

https://clinicaltrials.gov/show/NCT00309933

Keywords

Versions (1)
  1. 1/11/17 1/11/17 -
Uploaded on

January 11, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00309933

English

Eligibility Breast Cancer NCT00309933

1 forms  
Criteria
Description

Criteria

patient
Description

Patient

Data type

boolean

Alias
UMLS CUI [1]
C0030705
female breast cancer survivor with age at initial diagnosis in 1 of the following ranges:
Description

Female Breast Carcinoma Survivor | Age

Data type

boolean

Alias
UMLS CUI [1,1]
C0007104
UMLS CUI [1,2]
C0206194
UMLS CUI [2]
C0001779
18 to 45
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
55 to 78
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
must have enrolled and participated in ecog study clb-9741, e-1199, or e-2197
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
must have received chemotherapy at least 3 years, but no more than 8 years prior to this study entry
Description

Chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
disease free at the time of this study entry
Description

Disease Free of

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0332296
spouse or partner of the patient, age-matched female acquaintances of the patient (in the younger patient group), or partner of acquaintances
Description

Spouse | Partner | Acquaintance Female Age Similar | Partner Acquaintance

Data type

boolean

Alias
UMLS CUI [1]
C0162409
UMLS CUI [2]
C0682323
UMLS CUI [3,1]
C0337609
UMLS CUI [3,2]
C0086287
UMLS CUI [3,3]
C0001779
UMLS CUI [3,4]
C2348205
UMLS CUI [4,1]
C0682323
UMLS CUI [4,2]
C0337609
spouse or partner of the patient may be either gender
Description

Spouse Gender Both | Partner Gender Both

Data type

boolean

Alias
UMLS CUI [1,1]
C0162409
UMLS CUI [1,2]
C0079399
UMLS CUI [1,3]
C1706086
UMLS CUI [2,1]
C0682323
UMLS CUI [2,2]
C0079399
UMLS CUI [2,3]
C1706086
age-matched female acquaintance is defined as within 5 years of age difference of the patient in younger group (18-45 years of age)
Description

Acquaintance Female Age Similar

Data type

boolean

Alias
UMLS CUI [1,1]
C0337609
UMLS CUI [1,2]
C0086287
UMLS CUI [1,3]
C0001779
UMLS CUI [1,4]
C2348205
with a similar level of education and race of the patient
Description

Educational Status Similar | Racial group Similar

Data type

boolean

Alias
UMLS CUI [1,1]
C0013658
UMLS CUI [1,2]
C2348205
UMLS CUI [2,1]
C0034510
UMLS CUI [2,2]
C2348205
not a personal friend of the patient
Description

Friend Personal

Data type

boolean

Alias
UMLS CUI [1,1]
C0079382
UMLS CUI [1,2]
C1519021
no history of breast cancer
Description

Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0678222
patient characteristics:
Description

Client Characteristics

Data type

boolean

Alias
UMLS CUI [1]
C0815172
must reside in the continental u.s. and speak english (for patients)
Description

Residence United States continent | Able to speak English Language

Data type

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0041703
UMLS CUI [1,3]
C0454690
UMLS CUI [2,1]
C0564215
UMLS CUI [2,2]
C0376245
prior concurrent therapy:
Description

Therapeutic procedure

Data type

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Description

disease characteristic

Data type

boolean

Alias
UMLS CUI [1]
C0599878
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Similar models

Eligibility Breast Cancer NCT00309933

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient
Item
patient
boolean
C0030705 (UMLS CUI [1])
Female Breast Carcinoma Survivor | Age
Item
female breast cancer survivor with age at initial diagnosis in 1 of the following ranges:
boolean
C0007104 (UMLS CUI [1,1])
C0206194 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Age
Item
18 to 45
boolean
C0001779 (UMLS CUI [1])
Age
Item
55 to 78
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status
Item
must have enrolled and participated in ecog study clb-9741, e-1199, or e-2197
boolean
C2348568 (UMLS CUI [1])
Chemotherapy
Item
must have received chemotherapy at least 3 years, but no more than 8 years prior to this study entry
boolean
C0392920 (UMLS CUI [1])
Disease Free of
Item
disease free at the time of this study entry
boolean
C0012634 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
Spouse | Partner | Acquaintance Female Age Similar | Partner Acquaintance
Item
spouse or partner of the patient, age-matched female acquaintances of the patient (in the younger patient group), or partner of acquaintances
boolean
C0162409 (UMLS CUI [1])
C0682323 (UMLS CUI [2])
C0337609 (UMLS CUI [3,1])
C0086287 (UMLS CUI [3,2])
C0001779 (UMLS CUI [3,3])
C2348205 (UMLS CUI [3,4])
C0682323 (UMLS CUI [4,1])
C0337609 (UMLS CUI [4,2])
Spouse Gender Both | Partner Gender Both
Item
spouse or partner of the patient may be either gender
boolean
C0162409 (UMLS CUI [1,1])
C0079399 (UMLS CUI [1,2])
C1706086 (UMLS CUI [1,3])
C0682323 (UMLS CUI [2,1])
C0079399 (UMLS CUI [2,2])
C1706086 (UMLS CUI [2,3])
Acquaintance Female Age Similar
Item
age-matched female acquaintance is defined as within 5 years of age difference of the patient in younger group (18-45 years of age)
boolean
C0337609 (UMLS CUI [1,1])
C0086287 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
C2348205 (UMLS CUI [1,4])
Educational Status Similar | Racial group Similar
Item
with a similar level of education and race of the patient
boolean
C0013658 (UMLS CUI [1,1])
C2348205 (UMLS CUI [1,2])
C0034510 (UMLS CUI [2,1])
C2348205 (UMLS CUI [2,2])
Friend Personal
Item
not a personal friend of the patient
boolean
C0079382 (UMLS CUI [1,1])
C1519021 (UMLS CUI [1,2])
Breast Carcinoma
Item
no history of breast cancer
boolean
C0678222 (UMLS CUI [1])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Residence United States continent | Able to speak English Language
Item
must reside in the continental u.s. and speak english (for patients)
boolean
C0237096 (UMLS CUI [1,1])
C0041703 (UMLS CUI [1,2])
C0454690 (UMLS CUI [1,3])
C0564215 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
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