ID

38100

Beschrijving

Study of Survivorship Care Plans and Outcomes in Underserved Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT01627366

Link

https://clinicaltrials.gov/show/NCT01627366

Trefwoorden

Versies (1)
  1. 17-09-19 17-09-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

17 september 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01627366

Engels

Eligibility Breast Cancer NCT01627366

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
21 years of age or older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
english- or spanish-speaking
Beschrijving

Able to speak English Language | Able to speak Spanish Language

Datatype

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0564215
UMLS CUI [2,2]
C0037750
diagnosis of ductal carcinoma in situ (dcis) or stage i, ii, or iii bc for the first time
Beschrijving

DCIS | Breast Carcinoma Firstly TNM Breast tumor staging

Datatype

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C1279901
UMLS CUI [2,3]
C0474926
10-24 months post-diagnosis
Beschrijving

Time Period Elapsed Since Diagnosis

Datatype

boolean

Alias
UMLS CUI [1,1]
C1948053
UMLS CUI [1,2]
C1707889
UMLS CUI [1,3]
C1711239
UMLS CUI [1,4]
C0011900
at least 1 month post-chemotherapy completion
Beschrijving

Status post Chemotherapy Completion

Datatype

boolean

Alias
UMLS CUI [1,1]
C0231290
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0205197
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous cancer except non-melanomatous skin cancers or in situ non-breast cancers
Beschrijving

Malignant Neoplasms | Exception Skin carcinoma | Exception Carcinoma in Situ | Breast Carcinoma Excluded

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0007099
UMLS CUI [4,1]
C0678222
UMLS CUI [4,2]
C0332196
pregnant and lactating women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients receiving parenteral anti-cancer therapy, except trastuzumab
Beschrijving

Cancer treatment Parenteral | Exception Trastuzumab

Datatype

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C1518896
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0728747
clinically apparent cognitive or psychiatric impairment
Beschrijving

Impaired cognition | Impairment Psychiatric

Datatype

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2,1]
C0221099
UMLS CUI [2,2]
C0205487
participation in another research study
Beschrijving

Study Subject Participation Status | Research study

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0681814
current treatment for another cancer
Beschrijving

Therapeutic procedure Cancer Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C1707251
male
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
residing outside of los angeles county
Beschrijving

Residence Remote

Datatype

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0205157
too ill to participate
Beschrijving

Illness Severe | Study Subject Participation Status Excluded

Datatype

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C0332196
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Similar models

Eligibility Breast Cancer NCT01627366

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Age
Item
21 years of age or older
boolean
C0001779 (UMLS CUI [1])
Able to speak English Language | Able to speak Spanish Language
Item
english- or spanish-speaking
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0564215 (UMLS CUI [2,1])
C0037750 (UMLS CUI [2,2])
DCIS | Breast Carcinoma Firstly TNM Breast tumor staging
Item
diagnosis of ductal carcinoma in situ (dcis) or stage i, ii, or iii bc for the first time
boolean
C0007124 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C1279901 (UMLS CUI [2,2])
C0474926 (UMLS CUI [2,3])
Time Period Elapsed Since Diagnosis
Item
10-24 months post-diagnosis
boolean
C1948053 (UMLS CUI [1,1])
C1707889 (UMLS CUI [1,2])
C1711239 (UMLS CUI [1,3])
C0011900 (UMLS CUI [1,4])
Status post Chemotherapy Completion
Item
at least 1 month post-chemotherapy completion
boolean
C0231290 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Malignant Neoplasms | Exception Skin carcinoma | Exception Carcinoma in Situ | Breast Carcinoma Excluded
Item
previous cancer except non-melanomatous skin cancers or in situ non-breast cancers
boolean
C0006826 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0007099 (UMLS CUI [3,2])
C0678222 (UMLS CUI [4,1])
C0332196 (UMLS CUI [4,2])
Pregnancy | Breast Feeding
Item
pregnant and lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cancer treatment Parenteral | Exception Trastuzumab
Item
patients receiving parenteral anti-cancer therapy, except trastuzumab
boolean
C0920425 (UMLS CUI [1,1])
C1518896 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0728747 (UMLS CUI [2,2])
Impaired cognition | Impairment Psychiatric
Item
clinically apparent cognitive or psychiatric impairment
boolean
C0338656 (UMLS CUI [1])
C0221099 (UMLS CUI [2,1])
C0205487 (UMLS CUI [2,2])
Study Subject Participation Status | Research study
Item
participation in another research study
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2])
Therapeutic procedure Cancer Other
Item
current treatment for another cancer
boolean
C0087111 (UMLS CUI [1,1])
C1707251 (UMLS CUI [1,2])
Gender
Item
male
boolean
C0079399 (UMLS CUI [1])
Residence Remote
Item
residing outside of los angeles county
boolean
C0237096 (UMLS CUI [1,1])
C0205157 (UMLS CUI [1,2])
Illness Severe | Study Subject Participation Status Excluded
Item
too ill to participate
boolean
C0221423 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
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