Informações:
Falhas:
ID
13886
Descrição
Diabetes Care Management Compared to Standard Diabetes Care in Adolescents and Young Adults With Type 1 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01351857
Link
https://clinicaltrials.gov/show/NCT01351857
Palavras-chave
Versões (1)
- 13/03/2016 13/03/2016 -
Transferido a
13 de março de 2016
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Type 1 Diabetes NCT01351857
Eligibility Type 1 Diabetes NCT01351857
- StudyEvent: Eligibility
Similar models
Eligibility Type 1 Diabetes NCT01351857
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Diabetes type 1
Item
established t1d diagnosis for a minimum of one year (chosen to allow time for adjustment to a new diagnosis and more stable disease control).
boolean
C0011849 (UMLS CUI [1,1])
C0441729 (UMLS CUI [1,2])
C0441729 (UMLS CUI [1,2])
age
Item
between the ages of 17 and 20 years. it is left to the clinical judgment of the pediatric endocrinologist to determine individually the appropriate age of the transition for each subject
boolean
C0001779 (UMLS CUI [1])
consultation with pediatric endocrinologist
Item
at least 1 visit during the previous year with the pediatric endocrinologist at a diabetes clinic (aim is to minimize the non-adherence with the intervention).
boolean
C2107785 (UMLS CUI [1])
compliance
Item
ability to participate in all aspects of this clinical trial.
boolean
C1321605 (UMLS CUI [1])
informed consent
Item
written informed consent/assent must be obtained and documented.
boolean
C0021430 (UMLS CUI [1])
residence
Item
resident of ontario.
boolean
C0237096 (UMLS CUI [1])
pregnancy; lactating
Item
pregnant or lactating females or intent to become pregnant during the next 3 years.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Compliance behavior Limited Comorbidity
Item
conditions which in the opinion of the investigator may interfere with the subject's ability to participate in the study.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Study Subject Participation Status
Item
prior enrollment in the current study.
boolean
C2348568 (UMLS CUI [1])
Study Subject Participation Status
Item
current participation in another clinical trial or participation in another clinical trial in the 6 months prior to enrollment.
boolean
C2348568 (UMLS CUI [1])