ID

40720

Beschreibung

Resistance Exercise and Knee Osteoarthritis Pain, Functional Impairment and Cartilage Turnover; ODM derived from: https://clinicaltrials.gov/show/NCT01245283

Link

https://clinicaltrials.gov/show/NCT01245283

Stichworte

Versionen (1)
  1. 03.05.20 03.05.20 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

3. Mai 2020

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Knee Osteoarthritis NCT01245283

Englisch

Eligibility Knee Osteoarthritis NCT01245283

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
osteoarthritis (oa) of the knee for >6 months
Beschreibung

Knee Osteoarthritis Disease length

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0872146
moderate to severe pain immediately following a 50-foot walk
Beschreibung

Moderate pain | Severe pain | Status post Walk Distance

Datentyp

boolean

Alias
UMLS CUI [1]
C0278139
UMLS CUI [2]
C0278140
UMLS CUI [3,1]
C0231290
UMLS CUI [3,2]
C0080331
UMLS CUI [3,3]
C0012751
knee pain primarily due to tibiofemoral oa and not from patellofemoral oa
Beschreibung

Knee pain Due to Osteoarthritis Femorotibial joint | Absence Etiology Patellofemoral osteoarthritis

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0231749
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0029408
UMLS CUI [1,4]
C0447795
UMLS CUI [2,1]
C0332197
UMLS CUI [2,2]
C0015127
UMLS CUI [2,3]
C1542808
bilateral standing anterior-posterior radiograph demonstrating grade 2 or 3 oa of the target knee
Beschreibung

Knee Osteoarthritis Grade | X-rays of both knees, AP view, standing

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0441800
UMLS CUI [2]
C2322412
willing and able to participate in regular exercise for four months
Beschreibung

Participation Exercise Regular

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0015259
UMLS CUI [1,3]
C0205272
free from musculoskeletal limitations that would preclude resistance exercise participation
Beschreibung

Free of musculoskeletal problem | Participation Resistive exercise Possible

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0332296
UMLS CUI [1,2]
C0026859
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C0203991
UMLS CUI [2,3]
C0332149
free of abnormal cardiovascular responses during the screening graded maximal walk test
Beschreibung

Walk Test Grade Maximal | Free of Response Cardiovascular Abnormal

Datentyp

boolean

Alias
UMLS CUI [1,1]
C4277740
UMLS CUI [1,2]
C0441800
UMLS CUI [1,3]
C0205289
UMLS CUI [2,1]
C0332296
UMLS CUI [2,2]
C1704632
UMLS CUI [2,3]
C3887460
UMLS CUI [2,4]
C0205161
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable to walk
Beschreibung

Unable to walk

Datentyp

boolean

Alias
UMLS CUI [1]
C0560046
regular resistance exercise training (>3x week) within the past 6 months
Beschreibung

Resistive exercise Regular times per week

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0203991
UMLS CUI [1,2]
C0205272
UMLS CUI [1,3]
C0456698
specific low back pain or acute back injury
Beschreibung

Low Back Pain Specific | Back Injury

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0024031
UMLS CUI [1,2]
C0205369
UMLS CUI [2]
C0004601
spinal stenosis that precludes walking one block due to neurogenic claudication
Beschreibung

Spinal Stenosis Excludes Walking One Block | Etiology Neurogenic claudication

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0037944
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C3827522
UMLS CUI [2,1]
C0015127
UMLS CUI [2,2]
C0580173
any major injury to either knee within the prior 12 months
Beschreibung

Major injury Knee Either

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0332677
UMLS CUI [1,2]
C0022742
UMLS CUI [1,3]
C3844638
any surgery to either knee within the last 12 months
Beschreibung

Operative procedure on knee Either

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0187769
UMLS CUI [1,2]
C3844638
lumbar radiculopathy
Beschreibung

Lumbar radiculopathy

Datentyp

boolean

Alias
UMLS CUI [1]
C1263855
vascular claudication
Beschreibung

Intermittent Claudication

Datentyp

boolean

Alias
UMLS CUI [1]
C0021775
significant anterior knee pain due to diagnosed isolated patella-femoral syndrome or chondromalacia in either knee
Beschreibung

Anterior knee pain Due to Patellofemoral Syndrome | Anterior knee pain Due to Knee chondromalacia

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0409326
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0877149
UMLS CUI [2,1]
C0409326
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C2902706
have had corticosteroid or viscosupplement injections within three months of study participation
Beschreibung

Adrenal Cortex Hormones Injection | Viscosupplement Injection

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C1828121
UMLS CUI [2,1]
C2350506
UMLS CUI [2,2]
C1828121
have added new over the counter or prescription pain medication within two months of study participation
Beschreibung

Analgesics Non-Prescription Drugs | Analgesics Prescription Drugs

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0002771
UMLS CUI [1,2]
C0013231
UMLS CUI [2,1]
C0002771
UMLS CUI [2,2]
C0304227
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Knee Osteoarthritis NCT01245283

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Knee Osteoarthritis Disease length
Item
osteoarthritis (oa) of the knee for >6 months
boolean
C0409959 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Moderate pain | Severe pain | Status post Walk Distance
Item
moderate to severe pain immediately following a 50-foot walk
boolean
C0278139 (UMLS CUI [1])
C0278140 (UMLS CUI [2])
C0231290 (UMLS CUI [3,1])
C0080331 (UMLS CUI [3,2])
C0012751 (UMLS CUI [3,3])
Knee pain Due to Osteoarthritis Femorotibial joint | Absence Etiology Patellofemoral osteoarthritis
Item
knee pain primarily due to tibiofemoral oa and not from patellofemoral oa
boolean
C0231749 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0029408 (UMLS CUI [1,3])
C0447795 (UMLS CUI [1,4])
C0332197 (UMLS CUI [2,1])
C0015127 (UMLS CUI [2,2])
C1542808 (UMLS CUI [2,3])
Knee Osteoarthritis Grade | X-rays of both knees, AP view, standing
Item
bilateral standing anterior-posterior radiograph demonstrating grade 2 or 3 oa of the target knee
boolean
C0409959 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C2322412 (UMLS CUI [2])
Participation Exercise Regular
Item
willing and able to participate in regular exercise for four months
boolean
C0679823 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
Free of musculoskeletal problem | Participation Resistive exercise Possible
Item
free from musculoskeletal limitations that would preclude resistance exercise participation
boolean
C0332296 (UMLS CUI [1,1])
C0026859 (UMLS CUI [1,2])
C0679823 (UMLS CUI [2,1])
C0203991 (UMLS CUI [2,2])
C0332149 (UMLS CUI [2,3])
Walk Test Grade Maximal | Free of Response Cardiovascular Abnormal
Item
free of abnormal cardiovascular responses during the screening graded maximal walk test
boolean
C4277740 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0205289 (UMLS CUI [1,3])
C0332296 (UMLS CUI [2,1])
C1704632 (UMLS CUI [2,2])
C3887460 (UMLS CUI [2,3])
C0205161 (UMLS CUI [2,4])
Item Group
C0680251 (UMLS CUI)
Unable to walk
Item
unable to walk
boolean
C0560046 (UMLS CUI [1])
Resistive exercise Regular times per week
Item
regular resistance exercise training (>3x week) within the past 6 months
boolean
C0203991 (UMLS CUI [1,1])
C0205272 (UMLS CUI [1,2])
C0456698 (UMLS CUI [1,3])
Low Back Pain Specific | Back Injury
Item
specific low back pain or acute back injury
boolean
C0024031 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C0004601 (UMLS CUI [2])
Spinal Stenosis Excludes Walking One Block | Etiology Neurogenic claudication
Item
spinal stenosis that precludes walking one block due to neurogenic claudication
boolean
C0037944 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C3827522 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C0580173 (UMLS CUI [2,2])
Major injury Knee Either
Item
any major injury to either knee within the prior 12 months
boolean
C0332677 (UMLS CUI [1,1])
C0022742 (UMLS CUI [1,2])
C3844638 (UMLS CUI [1,3])
Operative procedure on knee Either
Item
any surgery to either knee within the last 12 months
boolean
C0187769 (UMLS CUI [1,1])
C3844638 (UMLS CUI [1,2])
Lumbar radiculopathy
Item
lumbar radiculopathy
boolean
C1263855 (UMLS CUI [1])
Intermittent Claudication
Item
vascular claudication
boolean
C0021775 (UMLS CUI [1])
Anterior knee pain Due to Patellofemoral Syndrome | Anterior knee pain Due to Knee chondromalacia
Item
significant anterior knee pain due to diagnosed isolated patella-femoral syndrome or chondromalacia in either knee
boolean
C0409326 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0877149 (UMLS CUI [1,3])
C0409326 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C2902706 (UMLS CUI [2,3])
Adrenal Cortex Hormones Injection | Viscosupplement Injection
Item
have had corticosteroid or viscosupplement injections within three months of study participation
boolean
C0001617 (UMLS CUI [1,1])
C1828121 (UMLS CUI [1,2])
C2350506 (UMLS CUI [2,1])
C1828121 (UMLS CUI [2,2])
Analgesics Non-Prescription Drugs | Analgesics Prescription Drugs
Item
have added new over the counter or prescription pain medication within two months of study participation
boolean
C0002771 (UMLS CUI [1,1])
C0013231 (UMLS CUI [1,2])
C0002771 (UMLS CUI [2,1])
C0304227 (UMLS CUI [2,2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video