ID

34687

Description

Effect of Internet Therapeutic Intervention on A1C Levels in Type 2 Diabetes Mellitus (DM) on Combination Oral Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01060241

Lien

https://clinicaltrials.gov/show/NCT01060241

Mots-clés

  1. 23/01/2019 23/01/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

23 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Type 2 Diabetes Mellitus NCT01060241

Eligibility Type 2 Diabetes Mellitus NCT01060241

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes patients treated with 2 or more oral anti-diabetic medication
Description

Diabetes Mellitus, Non-Insulin-Dependent | Antidiabetics Oral Quantity

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C1527415
UMLS CUI [2,3]
C1265611
a1c >7%
Description

Hemoglobin A1c measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0474680
>25 years of age
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
willingness to test blood glucose levels a minimum of 3 times daily
Description

Blood glucose measurement times/day Willing

Type de données

boolean

Alias
UMLS CUI [1,1]
C0392201
UMLS CUI [1,2]
C0439511
UMLS CUI [1,3]
C0600109
willingness to be randomized
Description

Randomization Willing

Type de données

boolean

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0600109
trained in self blood glucose monitoring
Description

Blood Glucose Self-Monitoring Experience

Type de données

boolean

Alias
UMLS CUI [1,1]
C0005803
UMLS CUI [1,2]
C0596545
internet access
Description

Access Internet

Type de données

boolean

Alias
UMLS CUI [1,1]
C0444454
UMLS CUI [1,2]
C0282111
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who do not meet the inclusion criteria or are not willing to participate will not be included in the study.
Description

Lacking Inclusion criteria Fulfill | Study Subject Participation Status Unwilling

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C1512693
UMLS CUI [1,3]
C1550543
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C0558080
in addition patients with the potential to become pregnant or patients using medications known to influence control of diabetes (eg steroids systemic or inhaled) are excluded from the study.
Description

Childbearing Potential | Pharmaceutical Preparations Influence Diabetes Control | Systemic steroids | Inhaled steroids

Type de données

boolean

Alias
UMLS CUI [1]
C3831118
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C4054723
UMLS CUI [2,3]
C0011847
UMLS CUI [2,4]
C0243148
UMLS CUI [3]
C2825233
UMLS CUI [4]
C2065041

Similar models

Eligibility Type 2 Diabetes Mellitus NCT01060241

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Antidiabetics Oral Quantity
Item
type 2 diabetes patients treated with 2 or more oral anti-diabetic medication
boolean
C0011860 (UMLS CUI [1])
C0935929 (UMLS CUI [2,1])
C1527415 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
Hemoglobin A1c measurement
Item
a1c >7%
boolean
C0474680 (UMLS CUI [1])
Age
Item
>25 years of age
boolean
C0001779 (UMLS CUI [1])
Blood glucose measurement times/day Willing
Item
willingness to test blood glucose levels a minimum of 3 times daily
boolean
C0392201 (UMLS CUI [1,1])
C0439511 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,3])
Randomization Willing
Item
willingness to be randomized
boolean
C0034656 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Blood Glucose Self-Monitoring Experience
Item
trained in self blood glucose monitoring
boolean
C0005803 (UMLS CUI [1,1])
C0596545 (UMLS CUI [1,2])
Access Internet
Item
internet access
boolean
C0444454 (UMLS CUI [1,1])
C0282111 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Lacking Inclusion criteria Fulfill | Study Subject Participation Status Unwilling
Item
patients who do not meet the inclusion criteria or are not willing to participate will not be included in the study.
boolean
C0332268 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
C2348568 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Childbearing Potential | Pharmaceutical Preparations Influence Diabetes Control | Systemic steroids | Inhaled steroids
Item
in addition patients with the potential to become pregnant or patients using medications known to influence control of diabetes (eg steroids systemic or inhaled) are excluded from the study.
boolean
C3831118 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C4054723 (UMLS CUI [2,2])
C0011847 (UMLS CUI [2,3])
C0243148 (UMLS CUI [2,4])
C2825233 (UMLS CUI [3])
C2065041 (UMLS CUI [4])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

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