ID

34439

Description

Preoperative Resistance Training in Patients Scheduled for Total Hip Arthroplasty; ODM derived from: https://clinicaltrials.gov/show/NCT01164111

Lien

https://clinicaltrials.gov/show/NCT01164111

Mots-clés

  1. 17/01/2019 17/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

17 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Osteoarthritis NCT01164111

Eligibility Osteoarthritis NCT01164111

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
all patients scheduled for total hip arthroplasty due to primary osteoarthritis with an age of 50 years or older.
Description

ID.1

Type de données

boolean

patients in the intervention group must participate in 80% of the training as a minimum and more than 2 skipped sessions in a row is not allowed.
Description

ID.2

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
rheumatoid arthritis (ra) or other types of arthritis other than primary osteoarthritis.
Description

ID.3

Type de données

boolean

uremia
Description

ID.4

Type de données

boolean

cancer
Description

ID.5

Type de données

boolean

systemic treatment with glucocorticoid more than 3 months the last 5 years with a daily dose > 5 mg.
Description

ID.6

Type de données

boolean

fracture of the hip (ipsi or contralateral)
Description

ID.7

Type de données

boolean

other fracture of the lower extremities the last year
Description

ID.8

Type de données

boolean

other condition with reduced function (ex polio seq.)
Description

ID.9

Type de données

boolean

weight above 135 kg
Description

ID.10

Type de données

boolean

Similar models

Eligibility Osteoarthritis NCT01164111

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
all patients scheduled for total hip arthroplasty due to primary osteoarthritis with an age of 50 years or older.
boolean
ID.2
Item
patients in the intervention group must participate in 80% of the training as a minimum and more than 2 skipped sessions in a row is not allowed.
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
rheumatoid arthritis (ra) or other types of arthritis other than primary osteoarthritis.
boolean
ID.4
Item
uremia
boolean
ID.5
Item
cancer
boolean
ID.6
Item
systemic treatment with glucocorticoid more than 3 months the last 5 years with a daily dose > 5 mg.
boolean
ID.7
Item
fracture of the hip (ipsi or contralateral)
boolean
ID.8
Item
other fracture of the lower extremities the last year
boolean
ID.9
Item
other condition with reduced function (ex polio seq.)
boolean
ID.10
Item
weight above 135 kg
boolean

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