Informações:
Falhas:
ID
38796
Descrição
Call-2-Health: Preventing Type II Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01827826
Link
https://clinicaltrials.gov/show/NCT01827826
Palavras-chave
Versões (1)
- 04/11/2019 04/11/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
4 de novembro de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT01827826
Eligibility Diabetes Mellitus, Type 2 NCT01827826
- StudyEvent: Eligibility
Similar models
Eligibility Diabetes Mellitus, Type 2 NCT01827826
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Age
Item
age 40-74
boolean
C0001779 (UMLS CUI [1])
Primary Health Care Medical center
Item
receives primary care at group health central, rainier, or poulsbo clinics in the greater seattle area
boolean
C0033137 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
C0565990 (UMLS CUI [1,2])
Able to walk Number of minutes
Item
can walk for more than 10 minutes
boolean
C2712089 (UMLS CUI [1,1])
C1562039 (UMLS CUI [1,2])
C1562039 (UMLS CUI [1,2])
Plasma fasting glucose measurement | Hemoglobin A1c measurement
Item
fasting plasma glucose (fpg) 105-125 mg/dl or glycolated hemoglobin (hba1c) 5.7-6.4
boolean
C0583513 (UMLS CUI [1])
C0474680 (UMLS CUI [2])
C0474680 (UMLS CUI [2])
Body mass index
Item
body mass index (bmi) 25 kg/m2 or greater
boolean
C1305855 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
type 1 or 2 diabetes
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0011860 (UMLS CUI [2])
Plasma fasting glucose measurement Blood draw
Item
fpg > 125 mg/dl or < 105mg/dl at screening blood draw
boolean
C0583513 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
Hemoglobin A1c measurement Blood draw
Item
hba1c > 6.4 or < 5.7 at screening blood draw
boolean
C0474680 (UMLS CUI [1,1])
C0005834 (UMLS CUI [1,2])
C0005834 (UMLS CUI [1,2])
Systolic Pressure
Item
systolic blood pressure > 210 mmhg at the baseline clinic visit
boolean
C0871470 (UMLS CUI [1])
Exercise Minutes per day Days per week
Item
exercise ≥ 30 minutes/day, at least five days a week
boolean
C0015259 (UMLS CUI [1,1])
C0556973 (UMLS CUI [1,2])
C0677547 (UMLS CUI [1,3])
C0556973 (UMLS CUI [1,2])
C0677547 (UMLS CUI [1,3])
Study Subject Participation Status | Weight Reduction Programs | Interventional Study
Item
current participation in another structured weight loss treatment program or another intervention study
boolean
C2348568 (UMLS CUI [1])
C3179079 (UMLS CUI [2])
C3274035 (UMLS CUI [3])
C3179079 (UMLS CUI [2])
C3274035 (UMLS CUI [3])
Comorbidity Severe
Item
severe concurrent disease
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
Patient unavailable Clinical Trial Period
Item
unavailable for the 24-week study period
boolean
C1301818 (UMLS CUI [1,1])
C2347804 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,2])
Lacking Able to read English Language | Lacking Able to speak English Language
Item
unable to read or speak english
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
Pregnancy | Pregnancy, Planned
Item
pregnant or planning to become pregnant.
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0032992 (UMLS CUI [2])
Mental handicap | Legal capacity Lacking | Informed Consent Unable
Item
mentally or legally incapacitated such that informed consent cannot be obtained.
boolean
C1306341 (UMLS CUI [1])
C0683673 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])
C0683673 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C1299582 (UMLS CUI [3,2])