Informatie:
Fout:
ID
35876
Beschrijving
Determining the Potential of Wholegrain Wheat and Rye to Improve Gut HealTh; ODM derived from: https://clinicaltrials.gov/show/NCT02358122
Link
https://clinicaltrials.gov/show/NCT02358122
Trefwoorden
Versies (1)
- 31-03-19 31-03-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
31 maart 2019
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Gastrointestinal Diseases NCT02358122
Eligibility Gastrointestinal Diseases NCT02358122
- StudyEvent: Eligibility
Similar models
Eligibility Gastrointestinal Diseases NCT02358122
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
• age: 30 - 65 years
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
body mass index (bmi): 25 - 32 kg/m2
boolean
C1305855 (UMLS CUI [1])
Stable body weight
Item
weight stable (<3 kg weight change during the last 6 months)
boolean
C0517386 (UMLS CUI [1])
Healthy
Item
apparently healthy
boolean
C3898900 (UMLS CUI [1])
Informed Consent
Item
informed consent signed
boolean
C0021430 (UMLS CUI [1])
Freezer Capacity Bread
Item
freezer capacity for 2 weeks bread provision
boolean
C0175738 (UMLS CUI [1,1])
C1516240 (UMLS CUI [1,2])
C0006138 (UMLS CUI [1,3])
C1516240 (UMLS CUI [1,2])
C0006138 (UMLS CUI [1,3])
Adherence Clinical Trial Visits
Item
can attend all visits required for the study
boolean
C1510802 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0008952 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,2])
C0008952 (UMLS CUI [1,3])
Tobacco use Daily
Item
• smoking on a daily basis
boolean
C0543414 (UMLS CUI [1,1])
C0332173 (UMLS CUI [1,2])
C0332173 (UMLS CUI [1,2])
Breast Feeding | Pregnancy | Pregnancy, Planned
Item
lactating (or lactating within 6 weeks prior to study start), pregnant (or pregnant within 3 months prior to study start) or wish to become pregnant during the study
boolean
C0006147 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0032961 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Diabetes Mellitus | Cardiovascular Diseases
Item
diagnosed with any form of diabetes or cvd
boolean
C0011849 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0007222 (UMLS CUI [2])
Gastrointestinal Diseases chronic
Item
reported chronic gi disorders
boolean
C0017178 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
C0205191 (UMLS CUI [1,2])
Antibiotic therapy
Item
antibiotic treatment 3 month before study start and during the study
boolean
C0338237 (UMLS CUI [1])
Prebiotics | Probiotics
Item
use of pre- or probiotic 1 month before study start and during the study
boolean
C2717875 (UMLS CUI [1])
C0525033 (UMLS CUI [2])
C0525033 (UMLS CUI [2])
Cooperation Lacking | Protocol Compliance Lacking
Item
lack of cooperation and adherence to the protocol
boolean
C0392337 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
C0332268 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
Prescription Drugs Evaluation
Item
use of prescription medication will be evaluated on an individual basis
boolean
C0304227 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C1261322 (UMLS CUI [1,2])