ID

34710

Description

Study to Test Use of a Decision Aid in a Clinical Visit to Help Patients Choose a Diabetes Medication; ODM derived from: https://clinicaltrials.gov/show/NCT01293578

Lien

https://clinicaltrials.gov/show/NCT01293578

Mots-clés

Versions (1)
  1. 24/01/2019 24/01/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

24 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Type 2 Diabetes Mellitus NCT01293578

Anglais

Eligibility Type 2 Diabetes Mellitus NCT01293578

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years of age and older
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
have a diagnosis of type 2 diabetes mellitus and on diabetes medication
Description

Diabetes Mellitus, Non-Insulin-Dependent | Antidiabetics

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2]
C0935929
have a diagnosis of type 2 diabetes mellitus for 1 year or more if not currently on diabetes medication
Description

Non-Insulin-Dependent Diabetes Mellitus Disease length | Antidiabetics Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C0872146
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C0332197
recognize their primary care provider as their main diabetes care provider
Description

Primary care provider Relationship Diabetes Mellitus

Type de données

boolean

Alias
UMLS CUI [1,1]
C2735026
UMLS CUI [1,2]
C0439849
UMLS CUI [1,3]
C0011849
use 0, 1, 2, or 3 oral hypoglycemic agents
Description

Oral hypoglycemics Quantity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0359086
UMLS CUI [1,2]
C1265611
have a recent hba1c measure (within 12 months) of greater than 7.3, with priority to patients with rising hba1c levels.
Description

Hemoglobin A1c measurement | Priority Elevated HbA1c

Type de données

boolean

Alias
UMLS CUI [1]
C0474680
UMLS CUI [2,1]
C0549179
UMLS CUI [2,2]
C4313270
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
not available for follow-up for 12 months after study visit.
Description

Patient unavailable Follow-up

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301818
UMLS CUI [1,2]
C3274571
unable to read and speak english.
Description

Lacking Able to read English Language | Lacking Able to speak English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0586740
UMLS CUI [1,3]
C0376245
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C0564215
UMLS CUI [2,3]
C0376245
has major barriers to providing written informed consent.
Description

Difficulty with Informed Consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332218
UMLS CUI [1,2]
C0021430
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Similar models

Eligibility Type 2 Diabetes Mellitus NCT01293578

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18 years of age and older
boolean
C0001779 (UMLS CUI [1])
Diabetes Mellitus, Non-Insulin-Dependent | Antidiabetics
Item
have a diagnosis of type 2 diabetes mellitus and on diabetes medication
boolean
C0011860 (UMLS CUI [1])
C0935929 (UMLS CUI [2])
Non-Insulin-Dependent Diabetes Mellitus Disease length | Antidiabetics Absent
Item
have a diagnosis of type 2 diabetes mellitus for 1 year or more if not currently on diabetes medication
boolean
C0011860 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
C0935929 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Primary care provider Relationship Diabetes Mellitus
Item
recognize their primary care provider as their main diabetes care provider
boolean
C2735026 (UMLS CUI [1,1])
C0439849 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,3])
Oral hypoglycemics Quantity
Item
use 0, 1, 2, or 3 oral hypoglycemic agents
boolean
C0359086 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Hemoglobin A1c measurement | Priority Elevated HbA1c
Item
have a recent hba1c measure (within 12 months) of greater than 7.3, with priority to patients with rising hba1c levels.
boolean
C0474680 (UMLS CUI [1])
C0549179 (UMLS CUI [2,1])
C4313270 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Patient unavailable Follow-up
Item
not available for follow-up for 12 months after study visit.
boolean
C1301818 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
Lacking Able to read English Language | Lacking Able to speak English Language
Item
unable to read and speak english.
boolean
C0332268 (UMLS CUI [1,1])
C0586740 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0332268 (UMLS CUI [2,1])
C0564215 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
Difficulty with Informed Consent
Item
has major barriers to providing written informed consent.
boolean
C0332218 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Retour au début de la page 

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