ID

13778

Description

Staying Active With Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT01280903

Lien

https://clinicaltrials.gov/show/NCT01280903

Mots-clés

  1. 06/03/2016 06/03/2016 -
Téléchargé le

6 mars 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Osteoarthritis, Knee NCT01280903

Eligibility Osteoarthritis, Knee NCT01280903

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 50 years or older.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
is community dwelling.
Description

community dwelling

Type de données

boolean

Alias
UMLS CUI [1]
C4045975
has osteoarthritis of the knee.
Description

Osteoarthritis, Knee

Type de données

boolean

Alias
UMLS CUI [1]
C0409959
has hypertension for which monotherapy or combination pharmacological treatment is prescribed.
Description

hypertension

Type de données

boolean

Alias
UMLS CUI [1]
C0020538
able to complete a behavioral run-in consisting of completing questionnaires, using a 7-day electronic-diary, and wearing an actigraph accelerometer at the waist for 7 days.
Description

compliance; Subject Diary

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C3890583
has written permission to participate from the physician.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
reports currently doing lower extremity exercise => 2 times/week.
Description

exercise lower extremity

Type de données

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C0023216
reports currently fitness walking => 90 minutes/week.
Description

walking

Type de données

boolean

Alias
UMLS CUI [1]
C0080331
incapable of managing their own treatment regimen.
Description

treatment regimen

Type de données

boolean

Alias
UMLS CUI [1]
C0040808
does not have, or cannot use, a telephone or is unwilling to provide a telephone number.
Description

telephone number

Type de données

boolean

Alias
UMLS CUI [1]
C1515258
has received cortisone or synvisc injections in the knee, angioplasty, stents, or a pacemaker in the past 6 months.
Description

injection cortisone; injection synvisc

Type de données

boolean

Alias
UMLS CUI [1,1]
C1272883
UMLS CUI [1,2]
C0010137
UMLS CUI [2,1]
C1272883
UMLS CUI [2,2]
C0723570
reports unstable cardiovascular, pulmonary, or metabolic disease or signs and symptoms suggestive of cardiovascular, pulmonary, or metabolic disease that restrict activity.
Description

cardiovascular disease; pulmonary disease; metabolic disease

Type de données

boolean

Alias
UMLS CUI [1]
C0007222
UMLS CUI [2]
C0024115
UMLS CUI [3]
C0025517
has resting systolic blood pressure => 160 mm hg or diastolic blood pressure => 100 mm hg.
Description

blood pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0005823
reports other conditions, such as osteoarthritis of the hip, spinal stenosis, inflammatory arthritis, foot drop, diabetes treated with insulin, or diabetic complications that may affect performance of lower extremity exercise and participation in fitness walking.
Description

hip osteoarthritis; spinal stenosis; Arthritis; foot drop; diabetes

Type de données

boolean

Alias
UMLS CUI [1]
C0029410
UMLS CUI [2]
C0037944
UMLS CUI [3]
C0003864
UMLS CUI [4]
C0011847
reports current knee conditions, such as meniscus tears and knee ligament ruptures.
Description

meniscus tears; knee ligament ruptures

Type de données

boolean

Alias
UMLS CUI [1]
C0238218
UMLS CUI [2]
C0263791
reports major depression that may impact the ability to fully participate in this study.
Description

Compliance behavior Limited major depression

Type de données

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1269683
is scheduled to undergo a major surgical procedure in the next 13 months.
Description

surgery

Type de données

boolean

Alias
UMLS CUI [1]
C0543467
is concurrently participating in a drug or psychoeducational trial that may confound, or be confounded by, participation in this study.
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Osteoarthritis, Knee NCT01280903

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
age 50 years or older.
boolean
C0001779 (UMLS CUI [1])
community dwelling
Item
is community dwelling.
boolean
C4045975 (UMLS CUI [1])
Osteoarthritis, Knee
Item
has osteoarthritis of the knee.
boolean
C0409959 (UMLS CUI [1])
hypertension
Item
has hypertension for which monotherapy or combination pharmacological treatment is prescribed.
boolean
C0020538 (UMLS CUI [1])
compliance; Subject Diary
Item
able to complete a behavioral run-in consisting of completing questionnaires, using a 7-day electronic-diary, and wearing an actigraph accelerometer at the waist for 7 days.
boolean
C1321605 (UMLS CUI [1])
C3890583 (UMLS CUI [2])
informed consent
Item
has written permission to participate from the physician.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
exercise lower extremity
Item
reports currently doing lower extremity exercise => 2 times/week.
boolean
C0015259 (UMLS CUI [1,1])
C0023216 (UMLS CUI [1,2])
walking
Item
reports currently fitness walking => 90 minutes/week.
boolean
C0080331 (UMLS CUI [1])
treatment regimen
Item
incapable of managing their own treatment regimen.
boolean
C0040808 (UMLS CUI [1])
telephone number
Item
does not have, or cannot use, a telephone or is unwilling to provide a telephone number.
boolean
C1515258 (UMLS CUI [1])
injection cortisone; injection synvisc
Item
has received cortisone or synvisc injections in the knee, angioplasty, stents, or a pacemaker in the past 6 months.
boolean
C1272883 (UMLS CUI [1,1])
C0010137 (UMLS CUI [1,2])
C1272883 (UMLS CUI [2,1])
C0723570 (UMLS CUI [2,2])
cardiovascular disease; pulmonary disease; metabolic disease
Item
reports unstable cardiovascular, pulmonary, or metabolic disease or signs and symptoms suggestive of cardiovascular, pulmonary, or metabolic disease that restrict activity.
boolean
C0007222 (UMLS CUI [1])
C0024115 (UMLS CUI [2])
C0025517 (UMLS CUI [3])
blood pressure
Item
has resting systolic blood pressure => 160 mm hg or diastolic blood pressure => 100 mm hg.
boolean
C0005823 (UMLS CUI [1])
hip osteoarthritis; spinal stenosis; Arthritis; foot drop; diabetes
Item
reports other conditions, such as osteoarthritis of the hip, spinal stenosis, inflammatory arthritis, foot drop, diabetes treated with insulin, or diabetic complications that may affect performance of lower extremity exercise and participation in fitness walking.
boolean
C0029410 (UMLS CUI [1])
C0037944 (UMLS CUI [2])
C0003864 (UMLS CUI [3])
C0011847 (UMLS CUI [4])
meniscus tears; knee ligament ruptures
Item
reports current knee conditions, such as meniscus tears and knee ligament ruptures.
boolean
C0238218 (UMLS CUI [1])
C0263791 (UMLS CUI [2])
Compliance behavior Limited major depression
Item
reports major depression that may impact the ability to fully participate in this study.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1269683 (UMLS CUI [1,3])
surgery
Item
is scheduled to undergo a major surgical procedure in the next 13 months.
boolean
C0543467 (UMLS CUI [1])
Study Subject Participation Status
Item
is concurrently participating in a drug or psychoeducational trial that may confound, or be confounded by, participation in this study.
boolean
C2348568 (UMLS CUI [1])

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