ID

33154

Beschreibung

Almonds and Diabetes Management; ODM derived from: https://clinicaltrials.gov/show/NCT01161030

Link

https://clinicaltrials.gov/show/NCT01161030

Stichworte

Versionen (1)
  1. 29.11.18 29.11.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

29. November 2018

DOI

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Creative Commons BY 4.0
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Eligibility Type 2 Diabetes NCT01161030

Englisch

Eligibility Type 2 Diabetes NCT01161030

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
12 subjects with diagnosed t2d for at least 1 year and 12 healthy individuals without t2d will be recruited for the acute almond trial.
Beschreibung

Almond Trial | Study Subject Quantity | Non-Insulin-Dependent Diabetes Mellitus Disease length | Healthy Volunteers Quantity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0440286
UMLS CUI [1,2]
C0008976
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0011860
UMLS CUI [3,2]
C0872146
UMLS CUI [4,1]
C1708335
UMLS CUI [4,2]
C1265611
24 subjects with diagnosed t2d for at least 1 year will be recruited for the chronic almond trial.
Beschreibung

Almond Trial chronic | Study Subject Quantity | Non-Insulin-Dependent Diabetes Mellitus Disease length

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0440286
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0205191
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0011860
UMLS CUI [3,2]
C0872146
subjects from the campus population and nearby communities will be recruited to participate in these trials.
Beschreibung

Patient Recruitment

Datentyp

boolean

Alias
UMLS CUI [1]
C0242800
men and women must be willing to comply with the experimental protocol including the restriction of nut consumption:
Beschreibung

Protocol Compliance | Restriction Nut Consumption

Datentyp

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2,1]
C0443288
UMLS CUI [2,2]
C0028723
UMLS CUI [2,3]
C0009830
subjects recruited for the acute almond study must agree not to consume any nuts or nut butters for 1-week prior to and during the 2-week trial
Beschreibung

Almond Trial | Nut Consumption Absent | Other Coding

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0440286
UMLS CUI [1,2]
C0008976
UMLS CUI [2,1]
C0028723
UMLS CUI [2,2]
C0009830
UMLS CUI [2,3]
C0332197
UMLS CUI [3]
C3846158
participants in the chronic almond study must agree not to consume nuts or nut butters more than 2 times per week during the 12 week trial.
Beschreibung

Almond Trial chronic | Nut Consumption Absent | Other Coding

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0440286
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0205191
UMLS CUI [2,1]
C0028723
UMLS CUI [2,2]
C0009830
UMLS CUI [2,3]
C0332197
UMLS CUI [3]
C3846158
participants must have a body mass index (bmi) from 20 to 35 kg/m2 and are aged 30 to 70 years.
Beschreibung

Body mass index | Age

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
UMLS CUI [2]
C0001779
subjects with t2d may take oral hyperglycemic agents.
Beschreibung

Diabetes Mellitus, Non-Insulin-Dependent | Oral hypoglycemic

Datentyp

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2]
C0359086
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
insulin use
Beschreibung

Insulin

Datentyp

boolean

Alias
UMLS CUI [1]
C0021641
history of a peanut allergy
Beschreibung

Allergy to peanuts

Datentyp

boolean

Alias
UMLS CUI [1]
C0559470
chronic or unresolved disease
Beschreibung

Chronic disease | Disease Without Resolution

Datentyp

boolean

Alias
UMLS CUI [1]
C0008679
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0332288
UMLS CUI [2,3]
C1514893
current smoking habit
Beschreibung

Smoking Habit

Datentyp

boolean

Alias
UMLS CUI [1]
C4505437
pregnant or lactating
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
medication use that may impact incretin secretion. [incretins are gastrointestinal hormones secreted at meal-time.]
Beschreibung

Pharmaceutical Preparations Impact Incretin secretion

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C4049986
UMLS CUI [1,3]
C1562292
UMLS CUI [1,4]
C0036536
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Ähnliche Modelle

Eligibility Type 2 Diabetes NCT01161030

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Almond Trial | Study Subject Quantity | Non-Insulin-Dependent Diabetes Mellitus Disease length | Healthy Volunteers Quantity
Item
12 subjects with diagnosed t2d for at least 1 year and 12 healthy individuals without t2d will be recruited for the acute almond trial.
boolean
C0440286 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0011860 (UMLS CUI [3,1])
C0872146 (UMLS CUI [3,2])
C1708335 (UMLS CUI [4,1])
C1265611 (UMLS CUI [4,2])
Almond Trial chronic | Study Subject Quantity | Non-Insulin-Dependent Diabetes Mellitus Disease length
Item
24 subjects with diagnosed t2d for at least 1 year will be recruited for the chronic almond trial.
boolean
C0440286 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0011860 (UMLS CUI [3,1])
C0872146 (UMLS CUI [3,2])
Patient Recruitment
Item
subjects from the campus population and nearby communities will be recruited to participate in these trials.
boolean
C0242800 (UMLS CUI [1])
Protocol Compliance | Restriction Nut Consumption
Item
men and women must be willing to comply with the experimental protocol including the restriction of nut consumption:
boolean
C0525058 (UMLS CUI [1])
C0443288 (UMLS CUI [2,1])
C0028723 (UMLS CUI [2,2])
C0009830 (UMLS CUI [2,3])
Almond Trial | Nut Consumption Absent | Other Coding
Item
subjects recruited for the acute almond study must agree not to consume any nuts or nut butters for 1-week prior to and during the 2-week trial
boolean
C0440286 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0028723 (UMLS CUI [2,1])
C0009830 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C3846158 (UMLS CUI [3])
Almond Trial chronic | Nut Consumption Absent | Other Coding
Item
participants in the chronic almond study must agree not to consume nuts or nut butters more than 2 times per week during the 12 week trial.
boolean
C0440286 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,3])
C0028723 (UMLS CUI [2,1])
C0009830 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C3846158 (UMLS CUI [3])
Body mass index | Age
Item
participants must have a body mass index (bmi) from 20 to 35 kg/m2 and are aged 30 to 70 years.
boolean
C1305855 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Diabetes Mellitus, Non-Insulin-Dependent | Oral hypoglycemic
Item
subjects with t2d may take oral hyperglycemic agents.
boolean
C0011860 (UMLS CUI [1])
C0359086 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Insulin
Item
insulin use
boolean
C0021641 (UMLS CUI [1])
Allergy to peanuts
Item
history of a peanut allergy
boolean
C0559470 (UMLS CUI [1])
Chronic disease | Disease Without Resolution
Item
chronic or unresolved disease
boolean
C0008679 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0332288 (UMLS CUI [2,2])
C1514893 (UMLS CUI [2,3])
Smoking Habit
Item
current smoking habit
boolean
C4505437 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Pharmaceutical Preparations Impact Incretin secretion
Item
medication use that may impact incretin secretion. [incretins are gastrointestinal hormones secreted at meal-time.]
boolean
C0013227 (UMLS CUI [1,1])
C4049986 (UMLS CUI [1,2])
C1562292 (UMLS CUI [1,3])
C0036536 (UMLS CUI [1,4])
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