ID

13779

Beschrijving

UCSD Take Charge Study; ODM derived from: https://clinicaltrials.gov/show/NCT01345500

Link

https://clinicaltrials.gov/show/NCT01345500

Trefwoorden

  1. 06-03-16 06-03-16 -
Geüploaded op

6 maart 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Overweight NCT01345500

Eligibility Overweight NCT01345500

  1. StudyEvent: Eligibility
    1. Eligibility Overweight NCT01345500
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18 years or older
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
type 2 diabetes
Beschrijving

diabetes type 2

Datatype

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0441730
bmi 25-45 kg/m2
Beschrijving

bmi

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
willing to participate in any of the study diet arms (higher or lower carbohydrate diet or usual care) over a one-year period
Beschrijving

compliance; carbohydrate diet

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0301577
able to comply with all required study procedures and schedule
Beschrijving

compliance

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
must live within the san diego or minneapolis area
Beschrijving

residence

Datatype

boolean

Alias
UMLS CUI [1]
C0237096
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant, breastfeeding or planning to become pregnant in the next year
Beschrijving

pregnancy; lactating

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
serious medical condition or psychiatric illness
Beschrijving

comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
history of having an eating disorder, food allergy or food intolerance
Beschrijving

eating disorder; Food Allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0013473
UMLS CUI [2]
C0016470
have food restrictions or requires a special diet
Beschrijving

special diet

Datatype

boolean

Alias
UMLS CUI [1]
C3164710
objects to frozen, processed or prepackaged foods
Beschrijving

frozen foods

Datatype

boolean

Alias
UMLS CUI [1]
C0016739
inability to be moderately physically active
Beschrijving

physically active

Datatype

boolean

Alias
UMLS CUI [1]
C0556453
currently enrolled in a weight loss program or another diet intervention
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
current use of weight loss medication or supplements
Beschrijving

concomitant medication

Datatype

boolean

Alias
UMLS CUI [1]
C2347852
planned surgical procedure that can impact the conduct of the study
Beschrijving

concurrent therapy surgery

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009429
UMLS CUI [1,2]
C0543467
previous surgical procedures for weight reduction
Beschrijving

surgery weight reduction

Datatype

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C1262477
does not have own transportation
Beschrijving

transportation

Datatype

boolean

Alias
UMLS CUI [1]
C0348005
have plans to relocate from area within 1 year
Beschrijving

address change

Datatype

boolean

Alias
UMLS CUI [1]
C1546916
hba1c >11%, fasting triglycerides >600 mg/dl, serum creatinine >1.4 mg/dl (women) or 1.5 mg/dl (men) -- to be screened at baseline visit
Beschrijving

hba1c; fasting triglycerides; serum creatinine

Datatype

boolean

Alias
UMLS CUI [1]
C0019018
UMLS CUI [2]
C0582824
UMLS CUI [3]
C0201976

Similar models

Eligibility Overweight NCT01345500

  1. StudyEvent: Eligibility
    1. Eligibility Overweight NCT01345500
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
aged 18 years or older
boolean
C0001779 (UMLS CUI [1])
diabetes type 2
Item
type 2 diabetes
boolean
C0011849 (UMLS CUI [1,1])
C0441730 (UMLS CUI [1,2])
bmi
Item
bmi 25-45 kg/m2
boolean
C1305855 (UMLS CUI [1])
compliance; carbohydrate diet
Item
willing to participate in any of the study diet arms (higher or lower carbohydrate diet or usual care) over a one-year period
boolean
C1321605 (UMLS CUI [1])
C0301577 (UMLS CUI [2])
compliance
Item
able to comply with all required study procedures and schedule
boolean
C1321605 (UMLS CUI [1])
residence
Item
must live within the san diego or minneapolis area
boolean
C0237096 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy; lactating
Item
pregnant, breastfeeding or planning to become pregnant in the next year
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
comorbidity
Item
serious medical condition or psychiatric illness
boolean
C0009488 (UMLS CUI [1])
eating disorder; Food Allergy
Item
history of having an eating disorder, food allergy or food intolerance
boolean
C0013473 (UMLS CUI [1])
C0016470 (UMLS CUI [2])
special diet
Item
have food restrictions or requires a special diet
boolean
C3164710 (UMLS CUI [1])
frozen foods
Item
objects to frozen, processed or prepackaged foods
boolean
C0016739 (UMLS CUI [1])
physically active
Item
inability to be moderately physically active
boolean
C0556453 (UMLS CUI [1])
Study Subject Participation Status
Item
currently enrolled in a weight loss program or another diet intervention
boolean
C2348568 (UMLS CUI [1])
concomitant medication
Item
current use of weight loss medication or supplements
boolean
C2347852 (UMLS CUI [1])
concurrent therapy surgery
Item
planned surgical procedure that can impact the conduct of the study
boolean
C0009429 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
surgery weight reduction
Item
previous surgical procedures for weight reduction
boolean
C0543467 (UMLS CUI [1,1])
C1262477 (UMLS CUI [1,2])
transportation
Item
does not have own transportation
boolean
C0348005 (UMLS CUI [1])
address change
Item
have plans to relocate from area within 1 year
boolean
C1546916 (UMLS CUI [1])
hba1c; fasting triglycerides; serum creatinine
Item
hba1c >11%, fasting triglycerides >600 mg/dl, serum creatinine >1.4 mg/dl (women) or 1.5 mg/dl (men) -- to be screened at baseline visit
boolean
C0019018 (UMLS CUI [1])
C0582824 (UMLS CUI [2])
C0201976 (UMLS CUI [3])

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