Informationen:
Fehler:
ID
40714
Beschreibung
Cognitive-behavioral (CBT) in ESRD Patients With Depression; ODM derived from: https://clinicaltrials.gov/show/NCT02011139
Link
https://clinicaltrials.gov/show/NCT02011139
Stichworte
Versionen (1)
- 02.05.20 02.05.20 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
2. Mai 2020
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Kidney Failure, Chronic NCT02011139
Eligibility Kidney Failure, Chronic NCT02011139
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Kidney Failure, Chronic NCT02011139
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Kidney Failure, Chronic | Hemodialysis
Item
patients with end-stage renal disease : on hemodialysis more than 3 months
boolean
C0022661 (UMLS CUI [1])
C0019004 (UMLS CUI [2])
C0019004 (UMLS CUI [2])
Beck Depression Inventory II score
Item
patients with bdi-ii score >= 15 points
boolean
C4273555 (UMLS CUI [1])
Adult | Age
Item
adult with age >= 20 years old
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Informed Consent
Item
patients who were able to understand and willing to sign the written informed consent
boolean
C0021430 (UMLS CUI [1])
Hemodialysis Due to Injury of kidney
Item
patients on hemodialysis due to acute kidney injury
boolean
C0019004 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0160420 (UMLS CUI [1,3])
C0678226 (UMLS CUI [1,2])
C0160420 (UMLS CUI [1,3])
Patient Admission
Item
patients who are on admission
boolean
C0030673 (UMLS CUI [1])
Chemotherapy Due to Malignant disease Progressive | Therapeutic radiology procedure Due to Malignant disease Progressive
Item
patients who are undergoing chemotherapy or radiation therapy due to progressive malignant disease
boolean
C0392920 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0442867 (UMLS CUI [1,3])
C0205329 (UMLS CUI [1,4])
C1522449 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0442867 (UMLS CUI [2,3])
C0205329 (UMLS CUI [2,4])
C0678226 (UMLS CUI [1,2])
C0442867 (UMLS CUI [1,3])
C0205329 (UMLS CUI [1,4])
C1522449 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0442867 (UMLS CUI [2,3])
C0205329 (UMLS CUI [2,4])
Kidney Transplantation Planned
Item
patients who are planning kidney transplantation within few months
boolean
C0022671 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,2])
Impaired cognition | Mental Retardation | Drug Dependence
Item
patients with cognitive dysfunction, mental retardation, and drug addict
boolean
C0338656 (UMLS CUI [1])
C0025362 (UMLS CUI [2])
C1510472 (UMLS CUI [3])
C0025362 (UMLS CUI [2])
C1510472 (UMLS CUI [3])
Patients Unavailable Communication Research Personnel
Item
patients who are unavailable for adequate communication with researchers
boolean
C0030705 (UMLS CUI [1,1])
C0686905 (UMLS CUI [1,2])
C0009452 (UMLS CUI [1,3])
C0035173 (UMLS CUI [1,4])
C0686905 (UMLS CUI [1,2])
C0009452 (UMLS CUI [1,3])
C0035173 (UMLS CUI [1,4])
Antidepressive Agents Changed | Antidepressive Agents Dose Changed
Item
patients who changed anti-depressive agent or dose within 2 months before/after the trial
boolean
C0003289 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C0003289 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0392747 (UMLS CUI [2,3])
C0392747 (UMLS CUI [1,2])
C0003289 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0392747 (UMLS CUI [2,3])