ID

33985

Descripción

Stress, Dietary Lapse and Weight Loss Among Adults With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00831194

Link

https://clinicaltrials.gov/show/NCT00831194

Palabras clave

Versiones (1)
  1. 10/1/19 10/1/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

10 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Obesity NCT00831194

Inglés

Eligibility Obesity NCT00831194

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00831194
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 21 to 65 years, seeking weight loss.
Descripción

Age | Weight loss Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C1262477
UMLS CUI [2,2]
C1301732
type 2 diabetes diagnosis by american diabetes association standard criteria. (confirmed by physician's note or blood glucose reports in previous year or prescriptions for medications to control blood glucose dated in participant's name within last year).
Descripción

Diabetes Mellitus, Non-Insulin-Dependent | Blood Glucose Report | Prescription of drug Blood Glucose Control

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0005802
UMLS CUI [2,2]
C0700287
UMLS CUI [3,1]
C2239117
UMLS CUI [3,2]
C0005802
UMLS CUI [3,3]
C0243148
bmi > 30 kg/m2.
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
major depression.
Descripción

Major Depressive Disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1269683
cognitive impairment severe enough to preclude informed consent or valid self report.
Descripción

Impaired cognition Excludes Informed Consent | Impaired cognition Excludes Validity of Self Report

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0338656
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0021430
UMLS CUI [2,1]
C0338656
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C1519944
use of medications that significantly affect appetite.
Descripción

Pharmaceutical Preparations Affecting Appetite

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0003618
eating disorder.
Descripción

Eating Disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013473
inability or unwillingness to use pda for 6 months.
Descripción

Use of PDA Unabe | Use of PDA Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C1136134
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C1524063
UMLS CUI [2,2]
C1136134
UMLS CUI [2,3]
C0558080
inability or unwillingness to collect saliva samples.
Descripción

Collection of sample of saliva Unable | Collection of sample of saliva Unwilling

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0455046
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0455046
UMLS CUI [2,2]
C0558080
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Similar models

Eligibility Obesity NCT00831194

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Obesity NCT00831194
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Age | Weight loss Planned
Item
age 21 to 65 years, seeking weight loss.
boolean
C0001779 (UMLS CUI [1])
C1262477 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Diabetes Mellitus, Non-Insulin-Dependent | Blood Glucose Report | Prescription of drug Blood Glucose Control
Item
type 2 diabetes diagnosis by american diabetes association standard criteria. (confirmed by physician's note or blood glucose reports in previous year or prescriptions for medications to control blood glucose dated in participant's name within last year).
boolean
C0011860 (UMLS CUI [1])
C0005802 (UMLS CUI [2,1])
C0700287 (UMLS CUI [2,2])
C2239117 (UMLS CUI [3,1])
C0005802 (UMLS CUI [3,2])
C0243148 (UMLS CUI [3,3])
Body mass index
Item
bmi > 30 kg/m2.
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Major Depressive Disorder
Item
major depression.
boolean
C1269683 (UMLS CUI [1])
Impaired cognition Excludes Informed Consent | Impaired cognition Excludes Validity of Self Report
Item
cognitive impairment severe enough to preclude informed consent or valid self report.
boolean
C0338656 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0338656 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C1519944 (UMLS CUI [2,3])
Pharmaceutical Preparations Affecting Appetite
Item
use of medications that significantly affect appetite.
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0003618 (UMLS CUI [1,3])
Eating Disorder
Item
eating disorder.
boolean
C0013473 (UMLS CUI [1])
Use of PDA Unabe | Use of PDA Unwilling
Item
inability or unwillingness to use pda for 6 months.
boolean
C1524063 (UMLS CUI [1,1])
C1136134 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1524063 (UMLS CUI [2,1])
C1136134 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
Collection of sample of saliva Unable | Collection of sample of saliva Unwilling
Item
inability or unwillingness to collect saliva samples.
boolean
C0455046 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0455046 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Volver a la parte superior de la página 

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