ID

43828

Description

Investigating Mechanisms to Explain Age Associated Differences in Quality of Life Among Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00582478

Lien

https://clinicaltrials.gov/show/NCT00582478

Mots-clés

  1. 05/05/2016 05/05/2016 -
  2. 18/06/2016 18/06/2016 -
  3. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Breast Cancer NCT00582478

Eligibility Breast Cancer NCT00582478

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Description

gender

Type de données

boolean

Alias
UMLS CUI [1]
C0086287
aged 18 or older at the time of breast cancer diagnosis
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
english-speaking
Description

english-speaking

Type de données

boolean

Alias
UMLS CUI [1]
C0376245
community dwelling (i.e. not living in a residential care or correctional facility)
Description

community dwelling

Type de données

boolean

Alias
UMLS CUI [1]
C4045975
diagnosed with invasive breast cancer stage i, ii, or iii within the previous 6 months
Description

invasive breast cancer stage

Type de données

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C3843634
first time diagnosis
Description

first time diagnosis

Type de données

boolean

Alias
UMLS CUI [1]
C0277556
have physician agreement for participation
Description

physician agreement for participation

Type de données

boolean

provide informed consent
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires
Description

abnormalitiy limitting informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0277577
previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer)
Description

previous or concurrent malignancy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C0006826
UMLS CUI [2,1]
C0205420
UMLS CUI [2,2]
C0006826
stage iv breast malignancy
Description

breast cancer stage IV

Type de données

boolean

Alias
UMLS CUI [1]
C0278488
residency outside of the united states
Description

residency

Type de données

boolean

Alias
UMLS CUI [1,1]
C0035182
UMLS CUI [1,2]
C3844068
for women ages 45 years and younger only: those participants < 45 years who were having regular menstrual cycles at the time of diagnosis will be excluded from this protocol. this study will only be enrolling women in this age category who have had a prior hysterectomy or were having irregular menstrual cycles at the time of diagnosis. women with regular menstrual cycles will be enrolled into a companion project (i.e., menstrual cycle maintenance
Description

irregular menstrual cyclus odr have had hysterectomy

Type de données

boolean

Similar models

Eligibility Breast Cancer NCT00582478

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
gender
Item
female
boolean
C0086287 (UMLS CUI [1])
age
Item
aged 18 or older at the time of breast cancer diagnosis
boolean
C0001779 (UMLS CUI [1])
english-speaking
Item
english-speaking
boolean
C0376245 (UMLS CUI [1])
community dwelling
Item
community dwelling (i.e. not living in a residential care or correctional facility)
boolean
C4045975 (UMLS CUI [1])
invasive breast cancer stage
Item
diagnosed with invasive breast cancer stage i, ii, or iii within the previous 6 months
boolean
C0011900 (UMLS CUI [1,1])
C3843634 (UMLS CUI [1,2])
first time diagnosis
Item
first time diagnosis
boolean
C0277556 (UMLS CUI [1])
physician agreement for participation
Item
have physician agreement for participation
boolean
informed consent
Item
provide informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
abnormalitiy limitting informed consent
Item
psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires
boolean
C0277577 (UMLS CUI [1])
previous or concurrent malignancy
Item
previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer)
boolean
C0205156 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
C0205420 (UMLS CUI [2,1])
C0006826 (UMLS CUI [2,2])
breast cancer stage IV
Item
stage iv breast malignancy
boolean
C0278488 (UMLS CUI [1])
residency
Item
residency outside of the united states
boolean
C0035182 (UMLS CUI [1,1])
C3844068 (UMLS CUI [1,2])
irregular menstrual cyclus odr have had hysterectomy
Item
for women ages 45 years and younger only: those participants < 45 years who were having regular menstrual cycles at the time of diagnosis will be excluded from this protocol. this study will only be enrolling women in this age category who have had a prior hysterectomy or were having irregular menstrual cycles at the time of diagnosis. women with regular menstrual cycles will be enrolled into a companion project (i.e., menstrual cycle maintenance
boolean

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