Eligibility Diabetes NCT01918345

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StudyEvent: Eligibility
1. Eligibility Diabetes NCT01918345

Name

Tipo

Description | Question | Decode (Coded Value)

Tipo de dados

Alias

Inclusion Criteria

Item Group

C1512693 (UMLS CUI)

Age

Item

18 years of age or older

boolean

C0001779 (UMLS CUI [1])

Gestational Diabetes | Pregnancy Most Recent

Item

physician-diagnosed gestational diabetes mellitus (gdm) during most recent pregnancy based on canadian diabetes association (cda) diagnostic criteria

boolean

C0085207 (UMLS CUI [1])
C0032961 (UMLS CUI [2,1])
C1513491 (UMLS CUI [2,2])

Postpartum Period | Status post Gestational Diabetes Pregnancy

Item

3-6 months postpartum after a gdm pregnancy

boolean

C0086839 (UMLS CUI [1])
C0231290 (UMLS CUI [2,1])
C0085207 (UMLS CUI [2,2])
C0032961 (UMLS CUI [2,3])

Gestational Diabetes Pregnancy | Followed by Diabetes in pregnancy clinic

Item

during gdm pregnancy, followed by a diabetes in pregnancy clinic at one of study sites (i.e. sunnybrook health sciences centre, mount sinai hospital, st. michael's hospital, toronto east general hospital)

boolean

C0085207 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C0332283 (UMLS CUI [2,1])
C3839840 (UMLS CUI [2,2])

Able to speak English Language

Item

english-speaking

boolean

C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])

Exclusion Criteria

Item Group

C0680251 (UMLS CUI)

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

Item

current diabetes (type i or type ii) and/or treatment with any anti-diabetic therapy

boolean

C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C3274787 (UMLS CUI [3])

Illness Major Interferes with Study Subject Participation Status

Item

any major illness that may interfere with participation

boolean

C0221423 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C0521102 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,4])

Obstetrical complication Interferes with Study Subject Participation Status | Complication Fetal Interferes with Study Subject Participation Status

Item

any obstetrical or fetal complication that may interfere with participation

boolean

C0178292 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0009566 (UMLS CUI [2,1])
C0521457 (UMLS CUI [2,2])
C0521102 (UMLS CUI [2,3])
C2348568 (UMLS CUI [2,4])

Study Subject Participation Status | Pharmacotherapy Required

Item

involvement in any other clinical trial requiring drug therapy

boolean

C2348568 (UMLS CUI [1])
C0013216 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])

Cardiovascular Disease | Progressive exercise test on treadmill ECG abnormal

Item

history of cardiovascular disease or ecg abnormalities on graded exercise treadmill test

boolean

C0007222 (UMLS CUI [1])
C0430507 (UMLS CUI [2,1])
C0522055 (UMLS CUI [2,2])

Pregnancy New | Postpartum Period

Item

new pregnancy within postpartum period

boolean

C0032961 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C0086839 (UMLS CUI [2])

Item

any illness affecting carbohydrate digestion and/or metabolism including kidney disease, hepatitis, hiv/aids, celiac disease

boolean

C0221423 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0007004 (UMLS CUI [1,3])
C0012238 (UMLS CUI [1,4])
C0221423 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0025519 (UMLS CUI [2,3])
C0022658 (UMLS CUI [3])
C0019158 (UMLS CUI [4])
C0019693 (UMLS CUI [5])
C0001175 (UMLS CUI [6])
C0007570 (UMLS CUI [7])

Factor Limiting Protocol Compliance

Item

any other factor likely to limit study adherence, in the opinion of the principal investigator

boolean

C1521761 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])

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Eligibility Diabetes NCT01918345