ID

15164

Descrição

Lifestyle Intervention and Prevention of Gestational Diabetes Mellitus; ODM derived from: https://clinicaltrials.gov/show/NCT02368600

Link

https://clinicaltrials.gov/show/NCT02368600

Palavras-chave

Versões (1)
  1. 20/05/2016 20/05/2016 -
Transferido a

20 de maio de 2016

DOI

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Licença

Creative Commons BY 4.0
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Eligibility Gestational Diabetes Mellitus NCT02368600

Inglês

Eligibility Gestational Diabetes Mellitus NCT02368600

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
chinese origin
Descrição

Chinese People

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0152035
reside normally in hong kong
Descrição

Resident Hong Kong

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2347958
UMLS CUI [1,2]
C0019907
singleton pregnancy
Descrição

Single pregnancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0341899
gestational age <= 12 weeks at the time of recruitment
Descrição

Gestational Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0017504
could speak and understand chinese
Descrição

Able to speak Chinese Language | Comprehension Chinese Language

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0008120
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C0008120
fulfill at least one of the following criteria for high risk of gdm at the time of recruitment based on the update hospital protocol implemented since 1st may 2014
Descrição

Gestational Diabetes High risk | criteria

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0085207
UMLS CUI [1,2]
C0332167
UMLS CUI [2]
C0243161
maternal age >= 35 years old at expected date of confinement.
Descrição

Maternal Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0024915
prior history of gdm or birth of child >= 4 kg
Descrição

Gestational Diabetes Past history | Birth Weight

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0085207
UMLS CUI [1,2]
C0332119
UMLS CUI [2]
C0005612
pre-pregnant bmi or bmi at 1st trimester >= 25 kg/m2
Descrição

Body mass index Before Pregnancy | Body mass index Pregnancy Trimester, First

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1305855
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C0032961
UMLS CUI [2,1]
C1305855
UMLS CUI [2,2]
C0032979
family history of diabetes at 1st degree relatives
Descrição

Family history of diabetes mellitus First Degree Relative

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1313937
UMLS CUI [1,2]
C1517194
willing to give informed written consent and follow the study procedures
Descrição

Informed Consent | Compliance behavior

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C1321605
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
concurrent participation in any clinical trial or study
Descrição

Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
with renal, liver or thyroid dysfunction, cognitive impairment, or any other indication of a major medical or psychological illness, as judged by the investigators as ineligible to participate the study
Descrição

Renal dysfunction | Liver Dysfunction | Thyroid dysfunction | Impaired cognition | Indication Illness Medical Major | Indication Illness Psychologic Major

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2]
C0086565
UMLS CUI [3]
C0348024
UMLS CUI [4]
C0338656
UMLS CUI [5,1]
C3146298
UMLS CUI [5,2]
C0221423
UMLS CUI [5,3]
C0205476
UMLS CUI [5,4]
C0205164
UMLS CUI [6,1]
C3146298
UMLS CUI [6,2]
C0221423
UMLS CUI [6,3]
C0205486
UMLS CUI [6,4]
C0205164
multiple pregnancies
Descrição

Multiple Pregnancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032989
pre-existing dm
Descrição

Diabetes Mellitus Pre-existing

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C2347662
with physical restriction that prevents from exercising
Descrição

Restriction Physical Preventing Exercise

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0443288
UMLS CUI [1,2]
C0205485
UMLS CUI [1,3]
C1292733
UMLS CUI [1,4]
C0015259
substance abuse
Descrição

Substance Use Disorders

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0038586
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Similar models

Eligibility Gestational Diabetes Mellitus NCT02368600

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Chinese People
Item
chinese origin
boolean
C0152035 (UMLS CUI [1])
Resident Hong Kong
Item
reside normally in hong kong
boolean
C2347958 (UMLS CUI [1,1])
C0019907 (UMLS CUI [1,2])
Single pregnancy
Item
singleton pregnancy
boolean
C0341899 (UMLS CUI [1])
Gestational Age
Item
gestational age <= 12 weeks at the time of recruitment
boolean
C0017504 (UMLS CUI [1])
Able to speak Chinese Language | Comprehension Chinese Language
Item
could speak and understand chinese
boolean
C0564215 (UMLS CUI [1,1])
C0008120 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0008120 (UMLS CUI [2,2])
Gestational Diabetes High risk | criteria
Item
fulfill at least one of the following criteria for high risk of gdm at the time of recruitment based on the update hospital protocol implemented since 1st may 2014
boolean
C0085207 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
C0243161 (UMLS CUI [2])
Maternal Age
Item
maternal age >= 35 years old at expected date of confinement.
boolean
C0024915 (UMLS CUI [1])
Gestational Diabetes Past history | Birth Weight
Item
prior history of gdm or birth of child >= 4 kg
boolean
C0085207 (UMLS CUI [1,1])
C0332119 (UMLS CUI [1,2])
C0005612 (UMLS CUI [2])
Body mass index Before Pregnancy | Body mass index Pregnancy Trimester, First
Item
pre-pregnant bmi or bmi at 1st trimester >= 25 kg/m2
boolean
C1305855 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0032961 (UMLS CUI [1,3])
C1305855 (UMLS CUI [2,1])
C0032979 (UMLS CUI [2,2])
Family history of diabetes mellitus First Degree Relative
Item
family history of diabetes at 1st degree relatives
boolean
C1313937 (UMLS CUI [1,1])
C1517194 (UMLS CUI [1,2])
Informed Consent | Compliance behavior
Item
willing to give informed written consent and follow the study procedures
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status
Item
concurrent participation in any clinical trial or study
boolean
C2348568 (UMLS CUI [1])
Renal dysfunction | Liver Dysfunction | Thyroid dysfunction | Impaired cognition | Indication Illness Medical Major | Indication Illness Psychologic Major
Item
with renal, liver or thyroid dysfunction, cognitive impairment, or any other indication of a major medical or psychological illness, as judged by the investigators as ineligible to participate the study
boolean
C3279454 (UMLS CUI [1])
C0086565 (UMLS CUI [2])
C0348024 (UMLS CUI [3])
C0338656 (UMLS CUI [4])
C3146298 (UMLS CUI [5,1])
C0221423 (UMLS CUI [5,2])
C0205476 (UMLS CUI [5,3])
C0205164 (UMLS CUI [5,4])
C3146298 (UMLS CUI [6,1])
C0221423 (UMLS CUI [6,2])
C0205486 (UMLS CUI [6,3])
C0205164 (UMLS CUI [6,4])
Multiple Pregnancy
Item
multiple pregnancies
boolean
C0032989 (UMLS CUI [1])
Diabetes Mellitus Pre-existing
Item
pre-existing dm
boolean
C0011849 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
Restriction Physical Preventing Exercise
Item
with physical restriction that prevents from exercising
boolean
C0443288 (UMLS CUI [1,1])
C0205485 (UMLS CUI [1,2])
C1292733 (UMLS CUI [1,3])
C0015259 (UMLS CUI [1,4])
Substance Use Disorders
Item
substance abuse
boolean
C0038586 (UMLS CUI [1])
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