ID

33176

Description

SWIFT: Study of Women, Infant Feeding and Type 2 Diabetes After GDM Pregnancy; ODM derived from: https://clinicaltrials.gov/show/NCT01967030

Link

https://clinicaltrials.gov/show/NCT01967030

Keywords

  1. 11/30/18 11/30/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

November 30, 2018

DOI

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License

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes NCT01967030

Eligibility Type 2 Diabetes NCT01967030

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 20 to 45 years at delivery
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
received prenatal care in kaiser permanente northern california (kpnc) health care system
Description

Prenatal care

Data type

boolean

Alias
UMLS CUI [1]
C0033052
gdm pregnancy diagnosed using the 3-hour 100 g ogtt by carpenter and coustan criteria
Description

Gestational Diabetes Pregnancy | Oral Glucose Tolerance Test

Data type

boolean

Alias
UMLS CUI [1,1]
C0085207
UMLS CUI [1,2]
C0032961
UMLS CUI [2]
C0029161
delivered a singleton, live birth >= 35 weeks gestation
Description

Childbirth Singleton | Live Birth Duration of gestation

Data type

boolean

Alias
UMLS CUI [1,1]
C1148523
UMLS CUI [1,2]
C1313913
UMLS CUI [2,1]
C0481667
UMLS CUI [2,2]
C0460089
no pre-existing diabetes or other serious medical conditions prior to index gdm pregnancy
Description

Pre-existing Diabetes mellitus Absent | Absence Other medical condition Serious Pre-existing

Data type

boolean

Alias
UMLS CUI [1,1]
C0455488
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0332197
UMLS CUI [2,2]
C3843040
UMLS CUI [2,3]
C0205404
UMLS CUI [2,4]
C2347662
no diabetes diagnosis (2-hour 75 gram ogtt) at 6 to 9 weeks postpartum for the index gdm pregnancy
Description

Absence Diabetes Mellitus Diagnosis Postpartum | Oral Glucose Tolerance Test

Data type

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0011849
UMLS CUI [1,3]
C0011900
UMLS CUI [1,4]
C0086839
UMLS CUI [2]
C0029161
no use of thyroid medications, steroids, or other medications affecting glucose tolerance
Description

Thyroid preparations Absent | Steroids Absent | Absence Pharmaceutical Preparations Affecting Glucose tolerance

Data type

boolean

Alias
UMLS CUI [1,1]
C0279175
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0038317
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0332197
UMLS CUI [3,2]
C0013227
UMLS CUI [3,3]
C0392760
UMLS CUI [3,4]
C0178665
not planning to move from the northern california area within the subsequent 24 months
Description

Relocation of home Plan Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
UMLS CUI [1,3]
C0332197
not planning another pregnancy within the next two years
Description

Planning Pregnancy Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0032992
UMLS CUI [1,2]
C0332197
two infant feeding groups: women who did not lactate or did so for less than 3 weeks, or women who provided no supplemental milk feeds at 2-4 weeks and planned to continue intensive lactation defined as <= 1 formula supplement (6 oz/day) from 6-9 weeks until 4 months or more postpartum.
Description

Infant feeding method Groups Quantity | Breast Feeding Absent | Breast Feeding Duration | Breast Feeding Supplemental Absent | Breast Feeding With intensity Planned | Infant formula feedings Amount

Data type

boolean

Alias
UMLS CUI [1,1]
C0420979
UMLS CUI [1,2]
C0441833
UMLS CUI [1,3]
C1265611
UMLS CUI [2,1]
C0006147
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0006147
UMLS CUI [3,2]
C0449238
UMLS CUI [4,1]
C0006147
UMLS CUI [4,2]
C2348609
UMLS CUI [4,3]
C0332197
UMLS CUI [5,1]
C0006147
UMLS CUI [5,2]
C0522510
UMLS CUI [5,3]
C1301732
UMLS CUI [6,1]
C4067712
UMLS CUI [6,2]
C1265611
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
women who fed breast milk and 7-16 oz of formula (mixed feeding) during the first 4 weeks of life
Description

Breast Feeding | Infant formula feedings Amount | Breast Feeding Mixed

Data type

boolean

Alias
UMLS CUI [1]
C0006147
UMLS CUI [2,1]
C4067712
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0006147
UMLS CUI [3,2]
C0205430

Similar models

Eligibility Type 2 Diabetes NCT01967030

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 20 to 45 years at delivery
boolean
C0001779 (UMLS CUI [1])
Prenatal care
Item
received prenatal care in kaiser permanente northern california (kpnc) health care system
boolean
C0033052 (UMLS CUI [1])
Gestational Diabetes Pregnancy | Oral Glucose Tolerance Test
Item
gdm pregnancy diagnosed using the 3-hour 100 g ogtt by carpenter and coustan criteria
boolean
C0085207 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0029161 (UMLS CUI [2])
Childbirth Singleton | Live Birth Duration of gestation
Item
delivered a singleton, live birth >= 35 weeks gestation
boolean
C1148523 (UMLS CUI [1,1])
C1313913 (UMLS CUI [1,2])
C0481667 (UMLS CUI [2,1])
C0460089 (UMLS CUI [2,2])
Pre-existing Diabetes mellitus Absent | Absence Other medical condition Serious Pre-existing
Item
no pre-existing diabetes or other serious medical conditions prior to index gdm pregnancy
boolean
C0455488 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [2,1])
C3843040 (UMLS CUI [2,2])
C0205404 (UMLS CUI [2,3])
C2347662 (UMLS CUI [2,4])
Absence Diabetes Mellitus Diagnosis Postpartum | Oral Glucose Tolerance Test
Item
no diabetes diagnosis (2-hour 75 gram ogtt) at 6 to 9 weeks postpartum for the index gdm pregnancy
boolean
C0332197 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C0086839 (UMLS CUI [1,4])
C0029161 (UMLS CUI [2])
Thyroid preparations Absent | Steroids Absent | Absence Pharmaceutical Preparations Affecting Glucose tolerance
Item
no use of thyroid medications, steroids, or other medications affecting glucose tolerance
boolean
C0279175 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0038317 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0332197 (UMLS CUI [3,1])
C0013227 (UMLS CUI [3,2])
C0392760 (UMLS CUI [3,3])
C0178665 (UMLS CUI [3,4])
Relocation of home Plan Absent
Item
not planning to move from the northern california area within the subsequent 24 months
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Planning Pregnancy Absent
Item
not planning another pregnancy within the next two years
boolean
C0032992 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Infant feeding method Groups Quantity | Breast Feeding Absent | Breast Feeding Duration | Breast Feeding Supplemental Absent | Breast Feeding With intensity Planned | Infant formula feedings Amount
Item
two infant feeding groups: women who did not lactate or did so for less than 3 weeks, or women who provided no supplemental milk feeds at 2-4 weeks and planned to continue intensive lactation defined as <= 1 formula supplement (6 oz/day) from 6-9 weeks until 4 months or more postpartum.
boolean
C0420979 (UMLS CUI [1,1])
C0441833 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0006147 (UMLS CUI [3,1])
C0449238 (UMLS CUI [3,2])
C0006147 (UMLS CUI [4,1])
C2348609 (UMLS CUI [4,2])
C0332197 (UMLS CUI [4,3])
C0006147 (UMLS CUI [5,1])
C0522510 (UMLS CUI [5,2])
C1301732 (UMLS CUI [5,3])
C4067712 (UMLS CUI [6,1])
C1265611 (UMLS CUI [6,2])
Item Group
C0680251 (UMLS CUI)
Breast Feeding | Infant formula feedings Amount | Breast Feeding Mixed
Item
women who fed breast milk and 7-16 oz of formula (mixed feeding) during the first 4 weeks of life
boolean
C0006147 (UMLS CUI [1])
C4067712 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0006147 (UMLS CUI [3,1])
C0205430 (UMLS CUI [3,2])

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