Informations:
Erreur:
ID
17563
Description
Intervention Study to Control High Blood Pressure for Korean American; ODM derived from: https://clinicaltrials.gov/show/NCT00473681
Lien
https://clinicaltrials.gov/show/NCT00473681
Mots-clés
Versions (2)
- 23/09/2016 23/09/2016 -
- 24/09/2016 24/09/2016 -
Téléchargé le
24 septembre 2016
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility High Blood Pressure NCT00473681
Eligibility High Blood Pressure NCT00473681
- StudyEvent: Eligibility
Similar models
Eligibility High Blood Pressure NCT00473681
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Korean American
Item
self-identified as first-generation korean american
boolean
C0597921 (UMLS CUI [1])
Age
Item
age 40 to 65 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure | Pharmaceutical Preparations Hypertensive disease
Item
sbp≥140 or dbp≥90mmhg on hbp medication
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0013227 (UMLS CUI [3,1])
C0020538 (UMLS CUI [3,2])
C0428883 (UMLS CUI [2])
C0013227 (UMLS CUI [3,1])
C0020538 (UMLS CUI [3,2])
Resident Baltimore
Item
resident of greater baltimore census tracts
boolean
C2347958 (UMLS CUI [1,1])
C0004716 (UMLS CUI [1,2])
C0004716 (UMLS CUI [1,2])
screening examination Consent
Item
written consent to participate in the screening/eligibility visit
boolean
C0281974 (UMLS CUI [1,1])
C1511481 (UMLS CUI [1,2])
C1511481 (UMLS CUI [1,2])
Systolic Pressure | Diastolic blood pressure | Hypertensive disease
Item
sbp≥140 or dbp≥90mmhg at the krc hbp verification visit
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0020538 (UMLS CUI [3])
C0428883 (UMLS CUI [2])
C0020538 (UMLS CUI [3])
Informed Consent | Protocol Compliance
Item
written consent to participate in the clinical trial:agreeing to participate in study data collection procedures, receiving hbp education, using hbpmt, and permitting contact with their own medical care provider.
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
C0525058 (UMLS CUI [2])
Condition Excludes participation | End stage cancer | Acute myocardial infarction
Item
acute and/or terminal condition precluding participation such as terminal cancer or acute myocardial infarction
boolean
C0348080 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0741884 (UMLS CUI [2])
C0155626 (UMLS CUI [3])
C0332196 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0741884 (UMLS CUI [2])
C0155626 (UMLS CUI [3])
Mental disorder Excludes participation | Schizophrenia | Impaired cognition
Item
psychiatric diagnosis precluding participation such as schizophrenia and cognitive impairment measured by self-report, chart review, or clinical assessment.
boolean
C0004936 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0036341 (UMLS CUI [2])
C0338656 (UMLS CUI [3])
C0332196 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0036341 (UMLS CUI [2])
C0338656 (UMLS CUI [3])