ID

18689

Beschreibung

Community-Based Programs for Improving Physical Function in People With Early Knee Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00586300

Link

https://clinicaltrials.gov/show/NCT00586300

Stichworte

Versionen (1)
  1. 16.11.16 16.11.16 -
Hochgeladen am

16. November 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00586300

Englisch

Eligibility Osteoarthritis NCT00586300

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
history of pain on most days (i.e., 4 or more days in a week) in one or both knees for at least 4 months during the year prior to study entry
Beschreibung

Knee pain Duration Frequency | Bilateral knee pain Duration Frequency

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0231749
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0376249
UMLS CUI [2,1]
C2220048
UMLS CUI [2,2]
C0449238
UMLS CUI [2,3]
C0376249
duration of symptoms (defined as pain on most days for at least 4 months in 1 year) of less than 5 years
Beschreibung

Pain Symptoms duration Frequency

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C0436359
UMLS CUI [1,3]
C0376249
radiographic evidence of grade ii knee oa
Beschreibung

Knee Osteoarthritis Evidence of | Kellgren-Lawrence score | Radiography

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0332120
UMLS CUI [2]
C3177117
UMLS CUI [3]
C0034571
some level of disability, represented as a score of 3 or higher for at least three of the following womac index items: descending or ascending stairs; walking; bending; and performing daily activities
Beschreibung

Disability Level | WOMAC scale Score | Able to walk down stairs | Able to walk up stairs | Able to walk | Able to bend | Performance of activities of daily living

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0231170
UMLS CUI [1,2]
C0441889
UMLS CUI [2,1]
C3472647
UMLS CUI [2,2]
C0449820
UMLS CUI [3]
C0560081
UMLS CUI [4]
C0560077
UMLS CUI [5]
C2712089
UMLS CUI [6]
C0560888
UMLS CUI [7]
C1821398
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any uncontrolled medical condition that could prevent safe participation in the study (e.g., uncontrolled heart disease, blood pressure, or respiratory conditions)
Beschreibung

Medical condition Uncontrolled At risk Study Subject Participation Status | Heart Disease Uncontrolled | Blood Pressure Uncontrolled | Respiratory condition Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0205318
UMLS CUI [1,3]
C1444641
UMLS CUI [1,4]
C2348568
UMLS CUI [2,1]
C0018799
UMLS CUI [2,2]
C0205318
UMLS CUI [3,1]
C0005823
UMLS CUI [3,2]
C0205318
UMLS CUI [4,1]
C4062804
UMLS CUI [4,2]
C0205318
any neurological condition that could affect coordination
Beschreibung

nervous system disorder Affecting Coordination

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027765
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0242414
inflammatory arthritis (e.g., rheumatoid or psoriatic arthritis)
Beschreibung

Arthritis | Rheumatoid Arthritis | Arthritis, Psoriatic

Datentyp

boolean

Alias
UMLS CUI [1]
C0003864
UMLS CUI [2]
C0003873
UMLS CUI [3]
C0003872
participates in aerobic activity or resistance training for more than 60 minutes per week
Beschreibung

Participates in aerobic exercise Duration Frequency | participation Resistance Training Duration Frequency

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1821481
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C0376249
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C0872279
UMLS CUI [2,3]
C0449238
UMLS CUI [2,4]
C0376249
history of knee surgery
Beschreibung

Operative procedure on knee

Datentyp

boolean

Alias
UMLS CUI [1]
C0187769
radiographic grade i, iii-iv (kellgren and lawrence classification)
Beschreibung

Kellgren-Lawrence score | Radiography

Datentyp

boolean

Alias
UMLS CUI [1]
C3177117
UMLS CUI [2]
C0034571
body mass index of at most 37.5 kg/m2 (individuals over this limit will be advised to follow a weight loss program and achieve stable weight for 6 months prior to participation.)
Beschreibung

Body mass index | Weight Reduction Program | Stable body weight

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
UMLS CUI [2]
C3179079
UMLS CUI [3]
C0517386
history of a knee corticosteroid injection in the 3 months prior to study entry
Beschreibung

corticosteroid injection into knee

Datentyp

boolean

Alias
UMLS CUI [1]
C2137761
plans to move from the local area
Beschreibung

Relocation of home Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
plans to become pregnant during the study
Beschreibung

Pregnancy, Planned

Datentyp

boolean

Alias
UMLS CUI [1]
C0032992
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Ähnliche Modelle

Eligibility Osteoarthritis NCT00586300

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Knee pain Duration Frequency | Bilateral knee pain Duration Frequency
Item
history of pain on most days (i.e., 4 or more days in a week) in one or both knees for at least 4 months during the year prior to study entry
boolean
C0231749 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0376249 (UMLS CUI [1,3])
C2220048 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0376249 (UMLS CUI [2,3])
Pain Symptoms duration Frequency
Item
duration of symptoms (defined as pain on most days for at least 4 months in 1 year) of less than 5 years
boolean
C0030193 (UMLS CUI [1,1])
C0436359 (UMLS CUI [1,2])
C0376249 (UMLS CUI [1,3])
Knee Osteoarthritis Evidence of | Kellgren-Lawrence score | Radiography
Item
radiographic evidence of grade ii knee oa
boolean
C0409959 (UMLS CUI [1,1])
C0332120 (UMLS CUI [1,2])
C3177117 (UMLS CUI [2])
C0034571 (UMLS CUI [3])
Disability Level | WOMAC scale Score | Able to walk down stairs | Able to walk up stairs | Able to walk | Able to bend | Performance of activities of daily living
Item
some level of disability, represented as a score of 3 or higher for at least three of the following womac index items: descending or ascending stairs; walking; bending; and performing daily activities
boolean
C0231170 (UMLS CUI [1,1])
C0441889 (UMLS CUI [1,2])
C3472647 (UMLS CUI [2,1])
C0449820 (UMLS CUI [2,2])
C0560081 (UMLS CUI [3])
C0560077 (UMLS CUI [4])
C2712089 (UMLS CUI [5])
C0560888 (UMLS CUI [6])
C1821398 (UMLS CUI [7])
Item Group
C0680251 (UMLS CUI)
Medical condition Uncontrolled At risk Study Subject Participation Status | Heart Disease Uncontrolled | Blood Pressure Uncontrolled | Respiratory condition Uncontrolled
Item
any uncontrolled medical condition that could prevent safe participation in the study (e.g., uncontrolled heart disease, blood pressure, or respiratory conditions)
boolean
C3843040 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,4])
C0018799 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0005823 (UMLS CUI [3,1])
C0205318 (UMLS CUI [3,2])
C4062804 (UMLS CUI [4,1])
C0205318 (UMLS CUI [4,2])
nervous system disorder Affecting Coordination
Item
any neurological condition that could affect coordination
boolean
C0027765 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0242414 (UMLS CUI [1,3])
Arthritis | Rheumatoid Arthritis | Arthritis, Psoriatic
Item
inflammatory arthritis (e.g., rheumatoid or psoriatic arthritis)
boolean
C0003864 (UMLS CUI [1])
C0003873 (UMLS CUI [2])
C0003872 (UMLS CUI [3])
Participates in aerobic exercise Duration Frequency | participation Resistance Training Duration Frequency
Item
participates in aerobic activity or resistance training for more than 60 minutes per week
boolean
C1821481 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0376249 (UMLS CUI [1,3])
C0679823 (UMLS CUI [2,1])
C0872279 (UMLS CUI [2,2])
C0449238 (UMLS CUI [2,3])
C0376249 (UMLS CUI [2,4])
Operative procedure on knee
Item
history of knee surgery
boolean
C0187769 (UMLS CUI [1])
Kellgren-Lawrence score | Radiography
Item
radiographic grade i, iii-iv (kellgren and lawrence classification)
boolean
C3177117 (UMLS CUI [1])
C0034571 (UMLS CUI [2])
Body mass index | Weight Reduction Program | Stable body weight
Item
body mass index of at most 37.5 kg/m2 (individuals over this limit will be advised to follow a weight loss program and achieve stable weight for 6 months prior to participation.)
boolean
C1305855 (UMLS CUI [1])
C3179079 (UMLS CUI [2])
C0517386 (UMLS CUI [3])
corticosteroid injection into knee
Item
history of a knee corticosteroid injection in the 3 months prior to study entry
boolean
C2137761 (UMLS CUI [1])
Relocation of home Planned
Item
plans to move from the local area
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Pregnancy, Planned
Item
plans to become pregnant during the study
boolean
C0032992 (UMLS CUI [1])
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