ID

35765

Descrição

Effect of Paired Testing to Poorly Controlled Chinese Diabetes on Glycemic Control and Self Care; ODM derived from: https://clinicaltrials.gov/show/NCT02225691

Link

https://clinicaltrials.gov/show/NCT02225691

Palavras-chave

Versões (1)
  1. 21/03/2019 21/03/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

21 de março de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Diabetes Mellitus, Type 2 NCT02225691

Inglês

Eligibility Diabetes Mellitus, Type 2 NCT02225691

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosed with diabetes mellitus
Descrição

Diabetes Mellitus

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0011849
hba1c ≥ 8% measured within the a month prior to enrolment
Descrição

Hemoglobin A1c measurement

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0474680
have not been performing smbg on a regular (daily) basis within the 3 months prior to enrolment
Descrição

Blood Glucose Self-Monitoring Regular Absent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0005803
UMLS CUI [1,2]
C0205272
UMLS CUI [1,3]
C0332197
willing and able to use accu-chek® active blood glucose meter to perform daily smbg
Descrição

Use of Accu-Chek Glucose Control Willing | Blood Glucose Self-Monitoring Daily Willing

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C0724912
UMLS CUI [1,3]
C0600109
UMLS CUI [2,1]
C0005803
UMLS CUI [2,2]
C0332173
UMLS CUI [2,3]
C0600109
willing and able to complete participant questionnaires
Descrição

Questionnaires Completion

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0034394
UMLS CUI [1,2]
C0205197
willing and able to visit the physician at month 3 and month 6
Descrição

Physician Visits

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0031831
UMLS CUI [1,2]
C0545082
provide informed consent prior to enrolling in the study
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
any retinopathy that required photocoagulation or retinal surgery in the 6 months prior to enrolment or that may require photocoagulation or retinal surgery during the study
Descrição

Retinal Disease Requirement Light Coagulation | Retinal Disease Requirement Operation on retina

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0035309
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0023694
UMLS CUI [2,1]
C0035309
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0197770
any clinically significant condition that required hospitalization in the last 2 months prior to enrolment or that may require hospitalization (e.g. elective surgery) during the study
Descrição

Medical condition Hospitalization Required | Elective Surgical Procedures

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C1708385
UMLS CUI [2]
C0206058
any clinically significant psychosis or cognitive impairment
Descrição

Psychotic Disorders | Impaired cognition

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0033975
UMLS CUI [2]
C0338656
unlikelihood to comply or complete the study
Descrição

Compliance behavior Unlikely | Completion of clinical trial Unlikely

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0750558
UMLS CUI [2,1]
C2732579
UMLS CUI [2,2]
C0750558
women who are pregnant, lactating or planning to become pregnant during the study period
Descrição

Pregnancy | Breast Feeding | Pregnancy, Planned

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
Voltar ao início da página

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT02225691

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus
Item
diagnosed with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
hba1c ≥ 8% measured within the a month prior to enrolment
boolean
C0474680 (UMLS CUI [1])
Blood Glucose Self-Monitoring Regular Absent
Item
have not been performing smbg on a regular (daily) basis within the 3 months prior to enrolment
boolean
C0005803 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Use of Accu-Chek Glucose Control Willing | Blood Glucose Self-Monitoring Daily Willing
Item
willing and able to use accu-chek® active blood glucose meter to perform daily smbg
boolean
C1524063 (UMLS CUI [1,1])
C0724912 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
C0005803 (UMLS CUI [2,1])
C0332173 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Questionnaires Completion
Item
willing and able to complete participant questionnaires
boolean
C0034394 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
Physician Visits
Item
willing and able to visit the physician at month 3 and month 6
boolean
C0031831 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
Informed Consent
Item
provide informed consent prior to enrolling in the study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Retinal Disease Requirement Light Coagulation | Retinal Disease Requirement Operation on retina
Item
any retinopathy that required photocoagulation or retinal surgery in the 6 months prior to enrolment or that may require photocoagulation or retinal surgery during the study
boolean
C0035309 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0023694 (UMLS CUI [1,3])
C0035309 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0197770 (UMLS CUI [2,3])
Medical condition Hospitalization Required | Elective Surgical Procedures
Item
any clinically significant condition that required hospitalization in the last 2 months prior to enrolment or that may require hospitalization (e.g. elective surgery) during the study
boolean
C3843040 (UMLS CUI [1,1])
C1708385 (UMLS CUI [1,2])
C0206058 (UMLS CUI [2])
Psychotic Disorders | Impaired cognition
Item
any clinically significant psychosis or cognitive impairment
boolean
C0033975 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
Compliance behavior Unlikely | Completion of clinical trial Unlikely
Item
unlikelihood to comply or complete the study
boolean
C1321605 (UMLS CUI [1,1])
C0750558 (UMLS CUI [1,2])
C2732579 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
women who are pregnant, lactating or planning to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial