ID

19216

Beschreibung

The Effects of a 16-Week Individualized, Intensive Strength Training Program in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00327275

Link

https://clinicaltrials.gov/show/NCT00327275

Stichworte

Versionen (1)
  1. 12.12.16 12.12.16 -
Hochgeladen am

12. Dezember 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00327275

Englisch

Eligibility Rheumatoid Arthritis NCT00327275

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
males and females with ra
Beschreibung

Rheumatoid Arthritis

Datentyp

boolean

Alias
UMLS CUI [1]
C0003873
over 18 years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
acr functional class i and ii
Beschreibung

Rheumatoid Arthritis Class Functional

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003873
UMLS CUI [1,2]
C0456387
UMLS CUI [1,3]
C0205245
taking remicade >4 months
Beschreibung

Remicade

Datentyp

boolean

Alias
UMLS CUI [1]
C0723012
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of comorbid conditions contraindicated to exercise, including, but not limited to:
Beschreibung

Medical contraindication Exercise

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0015259
1. heart disease
Beschreibung

Heart Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0018799
2. severe osteoporosis: (if >50 years): t score < -3.0 for hip or spine excluded; t score <-2.5 for hip or spine w/o current treatment)
Beschreibung

Severe osteoporosis T score | Severe osteoporosis T score Hip | Severe osteoporosis T score Vertebral column

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1859443
UMLS CUI [1,2]
C3854607
UMLS CUI [2,1]
C1859443
UMLS CUI [2,2]
C3854607
UMLS CUI [2,3]
C0019552
UMLS CUI [3,1]
C1859443
UMLS CUI [3,2]
C3854607
UMLS CUI [3,3]
C0037949
3. (all potential subjects) previous non-traumatic fractures
Beschreibung

Fracture

Datentyp

boolean

Alias
UMLS CUI [1]
C0016658
4. uncontrolled bp
Beschreibung

Blood Pressure Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005823
UMLS CUI [1,2]
C0205318
bmi >40
Beschreibung

Body mass index

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
regular use of assistive walking device which would interfere with ability to lift weights
Beschreibung

Walking assistive device Using Regular | Weight Lifting Ability Affected

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3874140
UMLS CUI [1,2]
C1524063
UMLS CUI [1,3]
C0205272
UMLS CUI [2,1]
C0043095
UMLS CUI [2,2]
C0085732
UMLS CUI [2,3]
C0392760
currently or within the last 3 months participating in aerobic exercise > 150 minutes a week
Beschreibung

Aerobic Exercise participation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0001701
UMLS CUI [1,2]
C0679823
currently or within the last 3 months participating in any regular strength training activities
Beschreibung

Resistance Training Regular participation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0872279
UMLS CUI [1,2]
C0205272
UMLS CUI [1,3]
C0679823
presence of neurological impairment that directly limits ability to perform exercise
Beschreibung

Neurologic Deficits Limiting Exercise

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0521654
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0015259
participation in concurrent exercise study
Beschreibung

Study Subject Participation Status | Clinical Trial Exercise

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0015259
any reason for which the investigator deems it would not be in the patient’s best interest to continue in the study
Beschreibung

Indication Discontinuation Clinical Trial

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0457454
UMLS CUI [1,3]
C0008976
plans to move away from site within next 1 year
Beschreibung

Relocation of home Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
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Ähnliche Modelle

Eligibility Rheumatoid Arthritis NCT00327275

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Rheumatoid Arthritis
Item
males and females with ra
boolean
C0003873 (UMLS CUI [1])
Age
Item
over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Rheumatoid Arthritis Class Functional
Item
acr functional class i and ii
boolean
C0003873 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0205245 (UMLS CUI [1,3])
Remicade
Item
taking remicade >4 months
boolean
C0723012 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Exercise
Item
presence of comorbid conditions contraindicated to exercise, including, but not limited to:
boolean
C1301624 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
Heart Disease
Item
1. heart disease
boolean
C0018799 (UMLS CUI [1])
Severe osteoporosis T score | Severe osteoporosis T score Hip | Severe osteoporosis T score Vertebral column
Item
2. severe osteoporosis: (if >50 years): t score < -3.0 for hip or spine excluded; t score <-2.5 for hip or spine w/o current treatment)
boolean
C1859443 (UMLS CUI [1,1])
C3854607 (UMLS CUI [1,2])
C1859443 (UMLS CUI [2,1])
C3854607 (UMLS CUI [2,2])
C0019552 (UMLS CUI [2,3])
C1859443 (UMLS CUI [3,1])
C3854607 (UMLS CUI [3,2])
C0037949 (UMLS CUI [3,3])
Fracture
Item
3. (all potential subjects) previous non-traumatic fractures
boolean
C0016658 (UMLS CUI [1])
Blood Pressure Uncontrolled
Item
4. uncontrolled bp
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Body mass index
Item
bmi >40
boolean
C1305855 (UMLS CUI [1])
Walking assistive device Using Regular | Weight Lifting Ability Affected
Item
regular use of assistive walking device which would interfere with ability to lift weights
boolean
C3874140 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
C0043095 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
Aerobic Exercise participation
Item
currently or within the last 3 months participating in aerobic exercise > 150 minutes a week
boolean
C0001701 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
Resistance Training Regular participation
Item
currently or within the last 3 months participating in any regular strength training activities
boolean
C0872279 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
Neurologic Deficits Limiting Exercise
Item
presence of neurological impairment that directly limits ability to perform exercise
boolean
C0521654 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Trial Exercise
Item
participation in concurrent exercise study
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0015259 (UMLS CUI [2,2])
Indication Discontinuation Clinical Trial
Item
any reason for which the investigator deems it would not be in the patient’s best interest to continue in the study
boolean
C0392360 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Relocation of home Planned
Item
plans to move away from site within next 1 year
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
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