ID

34409

Beschrijving

Nutrition, Neuromuscular Electrical Stimulation (NMES) and Secondary Progressive Multiple Sclerosis (SPMS); ODM derived from: https://clinicaltrials.gov/show/NCT01381354

Link

https://clinicaltrials.gov/show/NCT01381354

Trefwoorden

  1. 17-01-19 17-01-19 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT01381354

Eligibility Multiple Sclerosis NCT01381354

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
secondary or primary progressive multiple sclerosis
Beschrijving

ID.1

Datatype

boolean

some level of gait disability
Beschrijving

ID.2

Datatype

boolean

tolerance for test electrical therapy session
Beschrijving

ID.3

Datatype

boolean

successful completion of two week run-in phase completing the daily logs -
Beschrijving

ID.4

Datatype

boolean

demonstrating > 80% compliance with dietary and behavioral interventions
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
antiplatelet or blood thinning medication
Beschrijving

ID.6

Datatype

boolean

cognitive disability or psychiatric disorder making compliance with study interventions difficult
Beschrijving

ID.7

Datatype

boolean

implanted electronic medical device
Beschrijving

ID.8

Datatype

boolean

change in medication in the prior three months
Beschrijving

ID.9

Datatype

boolean

active cancer treatment (skin basal cell or squamous cancer is not an exclusion criteria)
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Multiple Sclerosis NCT01381354

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
secondary or primary progressive multiple sclerosis
boolean
ID.2
Item
some level of gait disability
boolean
ID.3
Item
tolerance for test electrical therapy session
boolean
ID.4
Item
successful completion of two week run-in phase completing the daily logs -
boolean
ID.5
Item
demonstrating > 80% compliance with dietary and behavioral interventions
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
antiplatelet or blood thinning medication
boolean
ID.7
Item
cognitive disability or psychiatric disorder making compliance with study interventions difficult
boolean
ID.8
Item
implanted electronic medical device
boolean
ID.9
Item
change in medication in the prior three months
boolean
ID.10
Item
active cancer treatment (skin basal cell or squamous cancer is not an exclusion criteria)
boolean

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