ID

30947

Beschrijving

Low Fat Diet and Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT00852722

Link

https://clinicaltrials.gov/show/NCT00852722

Trefwoorden

Versies (1)
  1. 06-07-18 06-07-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

6 juli 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT00852722

Engels

Eligibility Multiple Sclerosis NCT00852722

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinical diagnosis of the relapsing-remitting form of ms
Beschrijving

Multiple Sclerosis, Relapsing-Remitting

Datatype

boolean

Alias
UMLS CUI [1]
C0751967
age 18-70, inclusive
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ms duration of less than 15 years
Beschrijving

Multiple Sclerosis Duration

Datatype

boolean

Alias
UMLS CUI [1,1]
C0026769
UMLS CUI [1,2]
C0449238
may or may not be on disease-modifying therapies for ms, but if on, must be on for more than 6 months of continuous therapy
Beschrijving

Therapeutic procedure Multiple Sclerosis Modification | Absence Therapeutic procedure Multiple Sclerosis Modification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0026769
UMLS CUI [1,3]
C0392747
UMLS CUI [2,1]
C0332197
UMLS CUI [2,2]
C0087111
UMLS CUI [2,3]
C0026769
UMLS CUI [2,4]
C0392747
should not have diabetes
Beschrijving

Diabetes Mellitus Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0332197
able and willing to follow exercise instructions
Beschrijving

Exercise Instructions Adherence Able | Exercise Instructions Adherence Willing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C1442085
UMLS CUI [1,3]
C1510802
UMLS CUI [1,4]
C0085732
UMLS CUI [2,1]
C0015259
UMLS CUI [2,2]
C1442085
UMLS CUI [2,3]
C1510802
UMLS CUI [2,4]
C0600109
able and willing to travel to california for 10-day training program (cost covered by study)
Beschrijving

Training Program Duration Able | Training Program Duration Willing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0040607
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0085732
UMLS CUI [2,1]
C0040607
UMLS CUI [2,2]
C0449238
UMLS CUI [2,3]
C0600109
able and willing to travel to portland, or for 6 study visits over the 12 month study period (cost covered by study)
Beschrijving

Clinical Trial Visit Quantity Able | Clinical Trial Visit Quantity Willing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1512346
UMLS CUI [1,3]
C1265611
UMLS CUI [1,4]
C0085732
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C1512346
UMLS CUI [2,3]
C1265611
UMLS CUI [2,4]
C0600109
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
no clinically significant ms exacerbation within 30 days of screening visit
Beschrijving

Exacerbation of multiple sclerosis

Datatype

boolean

Alias
UMLS CUI [1]
C0581392
no systemically administered corticosteroids within 30 days of study entry
Beschrijving

CORTICOSTEROIDS FOR SYSTEMIC USE

Datatype

boolean

Alias
UMLS CUI [1]
C3653708
patient not pregnant or breastfeeding
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
not taking fish oil/flax seed for at least 2 months prior to first visit
Beschrijving

Fish Oils | Flaxseed

Datatype

boolean

Alias
UMLS CUI [1]
C0016157
UMLS CUI [2]
C0995001
no other significant health programs (e.g. active coronary heart disease, liver disease, pulmonary disease) that might increase risk of patient experiencing adverse events
Beschrijving

Coronary heart disease | Liver diseases | Lung diseases | Patient At risk Adverse event

Datatype

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2]
C0023895
UMLS CUI [3]
C0024115
UMLS CUI [4,1]
C0030705
UMLS CUI [4,2]
C1444641
UMLS CUI [4,3]
C0877248
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Similar models

Eligibility Multiple Sclerosis NCT00852722

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Multiple Sclerosis, Relapsing-Remitting
Item
clinical diagnosis of the relapsing-remitting form of ms
boolean
C0751967 (UMLS CUI [1])
Age
Item
age 18-70, inclusive
boolean
C0001779 (UMLS CUI [1])
Multiple Sclerosis Duration
Item
ms duration of less than 15 years
boolean
C0026769 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Therapeutic procedure Multiple Sclerosis Modification | Absence Therapeutic procedure Multiple Sclerosis Modification
Item
may or may not be on disease-modifying therapies for ms, but if on, must be on for more than 6 months of continuous therapy
boolean
C0087111 (UMLS CUI [1,1])
C0026769 (UMLS CUI [1,2])
C0392747 (UMLS CUI [1,3])
C0332197 (UMLS CUI [2,1])
C0087111 (UMLS CUI [2,2])
C0026769 (UMLS CUI [2,3])
C0392747 (UMLS CUI [2,4])
Diabetes Mellitus Absent
Item
should not have diabetes
boolean
C0011849 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Exercise Instructions Adherence Able | Exercise Instructions Adherence Willing
Item
able and willing to follow exercise instructions
boolean
C0015259 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
C1510802 (UMLS CUI [1,3])
C0085732 (UMLS CUI [1,4])
C0015259 (UMLS CUI [2,1])
C1442085 (UMLS CUI [2,2])
C1510802 (UMLS CUI [2,3])
C0600109 (UMLS CUI [2,4])
Training Program Duration Able | Training Program Duration Willing
Item
able and willing to travel to california for 10-day training program (cost covered by study)
boolean
C0040607 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C0040607 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Clinical Trial Visit Quantity Able | Clinical Trial Visit Quantity Willing
Item
able and willing to travel to portland, or for 6 study visits over the 12 month study period (cost covered by study)
boolean
C0008976 (UMLS CUI [1,1])
C1512346 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0085732 (UMLS CUI [1,4])
C0008976 (UMLS CUI [2,1])
C1512346 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0600109 (UMLS CUI [2,4])
Item Group
C0680251 (UMLS CUI)
Exacerbation of multiple sclerosis
Item
no clinically significant ms exacerbation within 30 days of screening visit
boolean
C0581392 (UMLS CUI [1])
CORTICOSTEROIDS FOR SYSTEMIC USE
Item
no systemically administered corticosteroids within 30 days of study entry
boolean
C3653708 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
patient not pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Fish Oils | Flaxseed
Item
not taking fish oil/flax seed for at least 2 months prior to first visit
boolean
C0016157 (UMLS CUI [1])
C0995001 (UMLS CUI [2])
Coronary heart disease | Liver diseases | Lung diseases | Patient At risk Adverse event
Item
no other significant health programs (e.g. active coronary heart disease, liver disease, pulmonary disease) that might increase risk of patient experiencing adverse events
boolean
C0010068 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0024115 (UMLS CUI [3])
C0030705 (UMLS CUI [4,1])
C1444641 (UMLS CUI [4,2])
C0877248 (UMLS CUI [4,3])
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