ID

34409

Descripción

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

Palabras clave

  1. 17/1/19 17/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

17 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT01381354

Eligibility Multiple Sclerosis NCT01381354

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
secondary or primary progressive multiple sclerosis
Descripción

ID.1

Tipo de datos

boolean

some level of gait disability
Descripción

ID.2

Tipo de datos

boolean

tolerance for test electrical therapy session
Descripción

ID.3

Tipo de datos

boolean

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

ID.4

Tipo de datos

boolean

demonstrating > 80% compliance with dietary and behavioral interventions
Descripción

ID.5

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
antiplatelet or blood thinning medication
Descripción

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

implanted electronic medical device
Descripción

ID.8

Tipo de datos

boolean

change in medication in the prior three months
Descripción

ID.9

Tipo de datos

boolean

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

ID.10

Tipo de datos

boolean

Similar models

Eligibility Multiple Sclerosis NCT01381354

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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