Informatie: Dit is niet de actueelste versie van het datamodel. Een versieoverzicht vindt u links onder Versies. De actueelste versie vindt u hier.
Informatie:
Fout:
ID
14897
Beschrijving
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
Trefwoorden
Versies (3)
- 05-05-16 05-05-16 -
- 18-06-16 18-06-16 -
- 20-09-21 20-09-21 -
Geüploaded op
5 mei 2016
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC-ND 3.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Breast Cancer NCT00582478
Eligibility Breast Cancer NCT00582478
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00582478
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ID.1
Item
female
boolean
C0015780 (UMLS CUI [1])
ID.2
Item
aged 18 or older at the time of breast cancer diagnosis
boolean
C0001779 (UMLS CUI [1])
ID.3
Item
english-speaking
boolean
C0376245 (UMLS CUI [1])
ID.4
Item
community dwelling (i.e. not living in a residential care or correctional facility)
boolean
C4045975 (UMLS CUI [1])
ID.5
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])
C3843634 (UMLS CUI [1,2])
ID.6
Item
first time diagnosis
boolean
C0277556 (UMLS CUI [1])
ID.7
Item
have physician agreement for participation
boolean
ID.8
Item
provide informed consent
boolean
C0021430 (UMLS CUI [1])
ID.9
Item
psychiatric or psychological abnormality precluding informed consent or ability to complete questionnaires
boolean
C0277577 (UMLS CUI [1])
ID.10
Item
previous or concurrent malignancy (except basal and squamous skin cancer and stage 0 cervical cancer)
boolean
C0205156 (UMLS CUI [1,1])
C0006826|C0205420 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C0006826|C0205420 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
ID.11
Item
stage iv breast malignancy
boolean
C0278488 (UMLS CUI [1])
ID.12
Item
residency outside of the united states
boolean
C0035182 (UMLS CUI [1,1])
C3844068 (UMLS CUI [1,2])
C3844068 (UMLS CUI [1,2])
ID.13
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