Englisch

Eligibility Prostate Cancer NCT02503748

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
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:
Beschreibung

Low Risk Prostate carcinoma Localized | Intermediate Risk Prostate carcinoma Localized

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3538919
UMLS CUI [1,2]
C0600139
UMLS CUI [1,3]
C0392752
UMLS CUI [2,1]
C3640764
UMLS CUI [2,2]
C0600139
UMLS CUI [2,3]
C0392752
tumor stage: clinical stage t1 or t2
Beschreibung

Tumor TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C3258246
psa level <20 (psa = prostata-specific antigen)
Beschreibung

Prostate specific antigen measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0201544
gleason score <8
Beschreibung

Gleason score

Datentyp

boolean

Alias
UMLS CUI [1]
C3203027
age ≤ 75 years
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
assumed life expectancy ≥ 10 years
Beschreibung

Life Expectancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0023671
other inclusion criteria due to the study design and the type of intervention are the following:
Beschreibung

Inclusion criteria Study Protocol | Inclusion criteria Type Intervention

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C2348563
UMLS CUI [2,1]
C1512693
UMLS CUI [2,2]
C0332307
UMLS CUI [2,3]
C0184661
diagnosis in one of the trial sites
Beschreibung

Diagnosis Clinical Study Site

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0011900
UMLS CUI [1,2]
C2347790
presence of an internet-enabled device in the home and basal operation knowledge of the corresponding device
Beschreibung

Internet Computer At home | Computer Operation Knowledge

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0282111
UMLS CUI [1,2]
C0009622
UMLS CUI [1,3]
C4534363
UMLS CUI [2,1]
C1880161
UMLS CUI [2,2]
C0376554
signing the consent form
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
impaired judgment
Beschreibung

Impaired judgement

Datentyp

boolean

Alias
UMLS CUI [1]
C0233818
insufficient ability to read and understand german
Beschreibung

Able to read German language Insufficient | Comprehension German language Insufficient

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0017477
UMLS CUI [1,3]
C0231180
UMLS CUI [2,1]
C0233733
UMLS CUI [2,2]
C0017477
UMLS CUI [2,3]
C0231180
emotional problems, which could lead to excessive demands by study participation
Beschreibung

Emotional problems | Study Subject Participation Status Limited

Datentyp

boolean

Alias
UMLS CUI [1]
C0677660
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C0439801
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Ähnliche Modelle

Eligibility Prostate Cancer NCT02503748

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
Tumor TNM clinical staging
Item
tumor stage: clinical stage t1 or t2
boolean
C0027651 (UMLS CUI [1,1])
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])
Diagnosis Clinical Study Site
Item
diagnosis in one of the trial sites
boolean
C0011900 (UMLS CUI [1,1])
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])
Informed Consent
Item
signing the consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
Zum Seitenanfang zurückkehren