ID

20278

Description

Muscle Strengthening Device for Knee Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00007241

Link

https://clinicaltrials.gov/show/NCT00007241

Keywords

Versions (1)
  1. 2/19/17 2/19/17 -
Uploaded on

February 19, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00007241

English

Eligibility Osteoarthritis NCT00007241

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
able to give conformed consent.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
age > 18.
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
pain symptoms provoked by activity in the more symptomatic knee of between (and inclusive of) 3/10 and 8/10 on a verbal analog scale.
Description

pain symptoms

Data type

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C0022742
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
participation in a strengthening program of the knees in the past month.
Description

study subject participation status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
uncontrolled or functionally limiting cardiac disease.
Description

cardiac disease

Data type

boolean

Alias
UMLS CUI [1]
C0018799
uncontrolled hypertension.
Description

uncontrolled hypertension

Data type

boolean

Alias
UMLS CUI [1]
C1868885
severe peripheral neuropathy (i.e., insensate to the simmes 5.07 monofilament).
Description

peripheral neuropathy

Data type

boolean

Alias
UMLS CUI [1]
C0031117
knee flexion contracture greater than 10 degrees.
Description

knee flexion

Data type

boolean

Alias
UMLS CUI [1,1]
C0409355
UMLS CUI [1,2]
C0449286
intra-articular steroids in the past 3 months, or hyaluronic acid in the last 9 months.
Description

intra-articular steroids

Data type

boolean

Alias
UMLS CUI [1,1]
C0038317
UMLS CUI [1,2]
C1522204
UMLS CUI [1,3]
C0020196
poor health that would impair compliance or assessment.
Description

poor health

Data type

boolean

Alias
UMLS CUI [1,1]
C0683321
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0439801
arthroscopy of either knee in the past six months.
Description

arthroscopy

Data type

boolean

Alias
UMLS CUI [1]
C1304878
lateral instability of > 15 degrees, or posterio-anterior instability of greater than 1 cm.
Description

lateral instability

Data type

boolean

Alias
UMLS CUI [1]
C2139206
knee pain due to pes anserine bursitis.
Description

pes anserine bursitis

Data type

boolean

Alias
UMLS CUI [1,1]
C4239663
UMLS CUI [1,2]
C0006444
active fibromyalgia.
Description

active fibromyalgia

Data type

boolean

Alias
UMLS CUI [1]
C0016053
active alcohol or substance abuse.
Description

substance abuse

Data type

boolean

Alias
UMLS CUI [1]
C0038586
arthritis other than osteoarthritis in the more symptomatic knee.
Description

arthritis

Data type

boolean

Alias
UMLS CUI [1]
C0240111
pregnancy.
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
history of cancer (other than skin cancer) not in remission.
Description

history of cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0006826
symptomatic spine, hip, ankle, or foot disease other than osteoarthritis that would interfere with assessment of the knee.
Description

symptoms

Data type

boolean

Alias
UMLS CUI [1]
C1457887
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Similar models

Eligibility Osteoarthritis NCT00007241

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
informed consent
Item
able to give conformed consent.
boolean
C0021430 (UMLS CUI [1])
age
Item
age > 18.
boolean
C0001779 (UMLS CUI [1])
pain symptoms
Item
pain symptoms provoked by activity in the more symptomatic knee of between (and inclusive of) 3/10 and 8/10 on a verbal analog scale.
boolean
C0030193 (UMLS CUI [1,1])
C0022742 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
study subject participation status
Item
participation in a strengthening program of the knees in the past month.
boolean
C2348568 (UMLS CUI [1])
cardiac disease
Item
uncontrolled or functionally limiting cardiac disease.
boolean
C0018799 (UMLS CUI [1])
uncontrolled hypertension
Item
uncontrolled hypertension.
boolean
C1868885 (UMLS CUI [1])
peripheral neuropathy
Item
severe peripheral neuropathy (i.e., insensate to the simmes 5.07 monofilament).
boolean
C0031117 (UMLS CUI [1])
knee flexion
Item
knee flexion contracture greater than 10 degrees.
boolean
C0409355 (UMLS CUI [1,1])
C0449286 (UMLS CUI [1,2])
intra-articular steroids
Item
intra-articular steroids in the past 3 months, or hyaluronic acid in the last 9 months.
boolean
C0038317 (UMLS CUI [1,1])
C1522204 (UMLS CUI [1,2])
C0020196 (UMLS CUI [1,3])
poor health
Item
poor health that would impair compliance or assessment.
boolean
C0683321 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
arthroscopy
Item
arthroscopy of either knee in the past six months.
boolean
C1304878 (UMLS CUI [1])
lateral instability
Item
lateral instability of > 15 degrees, or posterio-anterior instability of greater than 1 cm.
boolean
C2139206 (UMLS CUI [1])
pes anserine bursitis
Item
knee pain due to pes anserine bursitis.
boolean
C4239663 (UMLS CUI [1,1])
C0006444 (UMLS CUI [1,2])
active fibromyalgia
Item
active fibromyalgia.
boolean
C0016053 (UMLS CUI [1])
substance abuse
Item
active alcohol or substance abuse.
boolean
C0038586 (UMLS CUI [1])
arthritis
Item
arthritis other than osteoarthritis in the more symptomatic knee.
boolean
C0240111 (UMLS CUI [1])
pregnancy
Item
pregnancy.
boolean
C0032961 (UMLS CUI [1])
history of cancer
Item
history of cancer (other than skin cancer) not in remission.
boolean
C0262926 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
symptoms
Item
symptomatic spine, hip, ankle, or foot disease other than osteoarthritis that would interfere with assessment of the knee.
boolean
C1457887 (UMLS CUI [1])
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