ID

43828

Descripción

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

Link

https://clinicaltrials.gov/show/NCT00582478

Palabras clave

  1. 5/5/16 5/5/16 -
  2. 18/6/16 18/6/16 -
  3. 20/9/21 20/9/21 -
Subido en

20 de septiembre de 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Breast Cancer NCT00582478

Eligibility Breast Cancer NCT00582478

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
female
Descripción

gender

Tipo de datos

boolean

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

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
english-speaking
Descripción

english-speaking

Tipo de datos

boolean

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

community dwelling

Tipo de datos

boolean

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

invasive breast cancer stage

Tipo de datos

boolean

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

first time diagnosis

Tipo de datos

boolean

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

physician agreement for participation

Tipo de datos

boolean

provide informed consent
Descripción

informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

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

abnormalitiy limitting informed consent

Tipo de datos

boolean

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

previous or concurrent malignancy

Tipo de datos

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
Descripción

breast cancer stage IV

Tipo de datos

boolean

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

residency

Tipo de datos

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
Descripción

irregular menstrual cyclus odr have had hysterectomy

Tipo de datos

boolean

Similar models

Eligibility Breast Cancer NCT00582478

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial