ID

22142

Description

Climate Influence on Physiotherapy in Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT01057719

Link

https://clinicaltrials.gov/show/NCT01057719

Keywords

Versions (1)
  1. 5/21/17 5/21/17 -
Uploaded on

May 21, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT01057719

English

Eligibility Multiple Sclerosis NCT01057719

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
between 18 and 60 years of age (both included).
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
multiple sclerosis according to the mcdonald criteria
Description

multiple sclerosis mcdonald criteria

Data type

boolean

Alias
UMLS CUI [1,1]
C0026769
UMLS CUI [1,2]
C0243161
disability equivalent to expanded disability status score (edss) between 4.0 and 6.5 (both included)
Description

edss

Data type

boolean

Alias
UMLS CUI [1]
C0451246
prepared to and considered able to follow the protocol and to attend the planned visits during the whole study period.
Description

study compliance

Data type

boolean

Alias
UMLS CUI [1]
C1321605
given written informed consent
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
an active ms (attack or progression) during one month prior to inclusion or start of treatment.
Description

multiple sclerosis

Data type

boolean

Alias
UMLS CUI [1]
C0026769
received treatment with glucocorticoids the last month prior to inclusion or start of treatment.
Description

glucocorticoids

Data type

boolean

Alias
UMLS CUI [1]
C0017710
excessive fatigue or severe cognitive dysfunction related to ms that would preclude safe participation in the protocol.
Description

fatigue, cognitive dysfunction

Data type

boolean

Alias
UMLS CUI [1]
C0015672
UMLS CUI [2]
C0338656
suffered from major depression or any other psychiatric disorder that would preclude safe participation in the protocol.
Description

psychiatric disorder, major depression

Data type

boolean

Alias
UMLS CUI [1]
C0004936
UMLS CUI [2]
C1269683
heat intolerance.
Description

heat intolerance

Data type

boolean

Alias
UMLS CUI [1]
C0231274
other serious concomitant disease that could preclude safe participation in the protocol.
Description

concomitant disease

Data type

boolean

Alias
UMLS CUI [1]
C0243087
alcohol or drug abuse or consumption that could preclude participation according to the protocol and to attend the planned visits during the whole study period.
Description

alcohol or drug abuse

Data type

boolean

Alias
UMLS CUI [1]
C0038586
breastfeeding or pregnancy
Description

pregnancy, breast feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
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Similar models

Eligibility Multiple Sclerosis NCT01057719

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
between 18 and 60 years of age (both included).
boolean
C0001779 (UMLS CUI [1])
multiple sclerosis mcdonald criteria
Item
multiple sclerosis according to the mcdonald criteria
boolean
C0026769 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
edss
Item
disability equivalent to expanded disability status score (edss) between 4.0 and 6.5 (both included)
boolean
C0451246 (UMLS CUI [1])
study compliance
Item
prepared to and considered able to follow the protocol and to attend the planned visits during the whole study period.
boolean
C1321605 (UMLS CUI [1])
informed consent
Item
given written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
multiple sclerosis
Item
an active ms (attack or progression) during one month prior to inclusion or start of treatment.
boolean
C0026769 (UMLS CUI [1])
glucocorticoids
Item
received treatment with glucocorticoids the last month prior to inclusion or start of treatment.
boolean
C0017710 (UMLS CUI [1])
fatigue, cognitive dysfunction
Item
excessive fatigue or severe cognitive dysfunction related to ms that would preclude safe participation in the protocol.
boolean
C0015672 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
psychiatric disorder, major depression
Item
suffered from major depression or any other psychiatric disorder that would preclude safe participation in the protocol.
boolean
C0004936 (UMLS CUI [1])
C1269683 (UMLS CUI [2])
heat intolerance
Item
heat intolerance.
boolean
C0231274 (UMLS CUI [1])
concomitant disease
Item
other serious concomitant disease that could preclude safe participation in the protocol.
boolean
C0243087 (UMLS CUI [1])
alcohol or drug abuse
Item
alcohol or drug abuse or consumption that could preclude participation according to the protocol and to attend the planned visits during the whole study period.
boolean
C0038586 (UMLS CUI [1])
pregnancy, breast feeding
Item
breastfeeding or pregnancy
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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