Informações:
Falhas:
ID
36932
Descrição
Prostate Cancer E-Health-Tutorial; ODM derived from: https://clinicaltrials.gov/show/NCT02503748
Link
https://clinicaltrials.gov/show/NCT02503748
Palavras-chave
Versões (1)
- 21/06/2019 21/06/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
21 de junho de 2019
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Prostate Cancer NCT02503748
Eligibility Prostate Cancer NCT02503748
- StudyEvent: Eligibility
Similar models
Eligibility Prostate Cancer NCT02503748
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Low Risk Prostate carcinoma Localized | Intermediate Risk Prostate carcinoma Localized
Item
the study population consists of patients with a localized pros-tata carcinoma of the categories "low" or "intermediate risk", which are eligible for the aforementioned tutorial treatments in question, ie following medical criteria must be met:
boolean
C3538919 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
C0392752 (UMLS CUI [1,3])
C3640764 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
C0392752 (UMLS CUI [2,3])
C0600139 (UMLS CUI [1,2])
C0392752 (UMLS CUI [1,3])
C3640764 (UMLS CUI [2,1])
C0600139 (UMLS CUI [2,2])
C0392752 (UMLS CUI [2,3])
Tumor TNM clinical staging
Item
tumor stage: clinical stage t1 or t2
boolean
C0027651 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
Prostate specific antigen measurement
Item
psa level <20 (psa = prostata-specific antigen)
boolean
C0201544 (UMLS CUI [1])
Gleason score
Item
gleason score <8
boolean
C3203027 (UMLS CUI [1])
Age
Item
age ≤ 75 years
boolean
C0001779 (UMLS CUI [1])
Life Expectancy
Item
assumed life expectancy ≥ 10 years
boolean
C0023671 (UMLS CUI [1])
Inclusion criteria Study Protocol | Inclusion criteria Type Intervention
Item
other inclusion criteria due to the study design and the type of intervention are the following:
boolean
C1512693 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C1512693 (UMLS CUI [2,1])
C0332307 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
C2348563 (UMLS CUI [1,2])
C1512693 (UMLS CUI [2,1])
C0332307 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
Diagnosis Clinical Study Site
Item
diagnosis in one of the trial sites
boolean
C0011900 (UMLS CUI [1,1])
C2347790 (UMLS CUI [1,2])
C2347790 (UMLS CUI [1,2])
Internet Computer At home | Computer Operation Knowledge
Item
presence of an internet-enabled device in the home and basal operation knowledge of the corresponding device
boolean
C0282111 (UMLS CUI [1,1])
C0009622 (UMLS CUI [1,2])
C4534363 (UMLS CUI [1,3])
C1880161 (UMLS CUI [2,1])
C0376554 (UMLS CUI [2,2])
C0009622 (UMLS CUI [1,2])
C4534363 (UMLS CUI [1,3])
C1880161 (UMLS CUI [2,1])
C0376554 (UMLS CUI [2,2])
Informed Consent
Item
signing the consent form
boolean
C0021430 (UMLS CUI [1])
Impaired judgement
Item
impaired judgment
boolean
C0233818 (UMLS CUI [1])
Able to read German language Insufficient | Comprehension German language Insufficient
Item
insufficient ability to read and understand german
boolean
C0586740 (UMLS CUI [1,1])
C0017477 (UMLS CUI [1,2])
C0231180 (UMLS CUI [1,3])
C0233733 (UMLS CUI [2,1])
C0017477 (UMLS CUI [2,2])
C0231180 (UMLS CUI [2,3])
C0017477 (UMLS CUI [1,2])
C0231180 (UMLS CUI [1,3])
C0233733 (UMLS CUI [2,1])
C0017477 (UMLS CUI [2,2])
C0231180 (UMLS CUI [2,3])
Emotional problems | Study Subject Participation Status Limited
Item
emotional problems, which could lead to excessive demands by study participation
boolean
C0677660 (UMLS CUI [1])
C2348568 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C2348568 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])