ID

38796

Beschreibung

Call-2-Health: Preventing Type II Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01827826

Link

https://clinicaltrials.gov/show/NCT01827826

Stichworte

Versionen (1)
  1. 04.11.19 04.11.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

4. November 2019

DOI

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Eligibility Diabetes Mellitus, Type 2 NCT01827826

Englisch

Eligibility Diabetes Mellitus, Type 2 NCT01827826

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female
Beschreibung

Gender

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
age 40-74
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
receives primary care at group health central, rainier, or poulsbo clinics in the greater seattle area
Beschreibung

Primary Health Care Medical center

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0033137
UMLS CUI [1,2]
C0565990
can walk for more than 10 minutes
Beschreibung

Able to walk Number of minutes

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2712089
UMLS CUI [1,2]
C1562039
fasting plasma glucose (fpg) 105-125 mg/dl or glycolated hemoglobin (hba1c) 5.7-6.4
Beschreibung

Plasma fasting glucose measurement | Hemoglobin A1c measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0583513
UMLS CUI [2]
C0474680
body mass index (bmi) 25 kg/m2 or greater
Beschreibung

Body mass index

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
type 1 or 2 diabetes
Beschreibung

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Datentyp

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
fpg > 125 mg/dl or < 105mg/dl at screening blood draw
Beschreibung

Plasma fasting glucose measurement Blood draw

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0583513
UMLS CUI [1,2]
C0005834
hba1c > 6.4 or < 5.7 at screening blood draw
Beschreibung

Hemoglobin A1c measurement Blood draw

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0474680
UMLS CUI [1,2]
C0005834
systolic blood pressure > 210 mmhg at the baseline clinic visit
Beschreibung

Systolic Pressure

Datentyp

boolean

Alias
UMLS CUI [1]
C0871470
exercise ≥ 30 minutes/day, at least five days a week
Beschreibung

Exercise Minutes per day Days per week

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C0556973
UMLS CUI [1,3]
C0677547
current participation in another structured weight loss treatment program or another intervention study
Beschreibung

Study Subject Participation Status | Weight Reduction Programs | Interventional Study

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C3179079
UMLS CUI [3]
C3274035
severe concurrent disease
Beschreibung

Comorbidity Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
unavailable for the 24-week study period
Beschreibung

Patient unavailable Clinical Trial Period

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301818
UMLS CUI [1,2]
C2347804
unable to read or speak english
Beschreibung

Lacking Able to read English Language | Lacking Able to speak English Language

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C0564215
UMLS CUI [2,3]
C0376245
pregnant or planning to become pregnant.
Beschreibung

Pregnancy | Pregnancy, Planned

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
mentally or legally incapacitated such that informed consent cannot be obtained.
Beschreibung

Mental handicap | Legal capacity Lacking | Informed Consent Unable

Datentyp

boolean

Alias
UMLS CUI [1]
C1306341
UMLS CUI [2,1]
C0683673
UMLS CUI [2,2]
C0332268
UMLS CUI [3,1]
C0021430
UMLS CUI [3,2]
C1299582
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Ähnliche Modelle

Eligibility Diabetes Mellitus, Type 2 NCT01827826

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
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])
Body mass index
Item
body mass index (bmi) 25 kg/m2 or greater
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
type 1 or 2 diabetes
boolean
C0011854 (UMLS CUI [1])
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])
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])
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])
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])
Comorbidity Severe
Item
severe concurrent disease
boolean
C0009488 (UMLS CUI [1,1])
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])
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])
Pregnancy | Pregnancy, Planned
Item
pregnant or planning to become pregnant.
boolean
C0032961 (UMLS CUI [1])
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])
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