ID

42620

Beschreibung

Effects of Aerobic Exercise Versus Weight Training in Breast Cancer Survivors During Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT00115713

Link

https://clinicaltrials.gov/show/NCT00115713

Stichworte

Versionen (2)
  1. 17.07.16 17.07.16 -
  2. 17.09.21 17.09.21 -
Hochgeladen am

17. September 2021

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 Breast Neoplasms NCT00115713

Englisch

Eligibility Breast Neoplasms NCT00115713

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
breast cancer early stage i –iiia
Beschreibung

Early-Stage Breast Carcinoma | TNM clinical staging

Datentyp

boolean

Alias
UMLS CUI [1]
C2986665
UMLS CUI [2]
C3258246
completed axillary surgery
Beschreibung

Operative Surgical Procedure Axillary Completed

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0004454
UMLS CUI [1,3]
C0205197
scheduled to receive adjuvant chemotherapy for 9 – 24 weeks
Beschreibung

Adjuvant Chemotherapy Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0085533
UMLS CUI [1,2]
C1301732
approval of the treating oncologist
Beschreibung

Approval Oncologist Treating

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205540
UMLS CUI [1,2]
C0259990
UMLS CUI [1,3]
C1522326
able to understand and provide written informed consent in english or french (ottawa)
Beschreibung

Comprehension English Language | Comprehension French language | Informed Consent English Language | Informed Consent French language

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C0376246
UMLS CUI [3,1]
C0021430
UMLS CUI [3,2]
C0376245
UMLS CUI [4,1]
C0021430
UMLS CUI [4,2]
C0376246
18+ years of age
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
no uncontrolled hypertension, cardiac illness, psychiatric condition
Beschreibung

Uncontrolled hypertension | Heart Diseases | Mental disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C1868885
UMLS CUI [2]
C0018799
UMLS CUI [3]
C0004936
no contraindication to exercise as determined by a fitness test
Beschreibung

Medical contraindication Exercise | Fitness Test

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0015259
UMLS CUI [2,1]
C0031812
UMLS CUI [2,2]
C0456984
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant.
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
unwilling to accept randomization.
Beschreibung

Randomization Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0558080
any medical condition that would be a contraindication to exercise. the clinicians will make this decision.
Beschreibung

medical condition Contraindication Exercise

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0015259
unwilling to travel to/participate in the exercise program as defined by the protocol.
Beschreibung

Exercise Program participation Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0015259
UMLS CUI [1,2]
C3484370
UMLS CUI [1,3]
C0679823
UMLS CUI [1,4]
C0558080
previous chemotherapy (previous cancer is not an exclusion criteria).
Beschreibung

Prior Chemotherapy | Malignant Neoplasms

Datentyp

boolean

Alias
UMLS CUI [1]
C1514457
UMLS CUI [2]
C0006826
cancer recurrence.
Beschreibung

cancer recurrence

Datentyp

boolean

Alias
UMLS CUI [1]
C0920420
planned/known absence of greater than 2 weeks during the intended study period.
Beschreibung

Clinical Trial Patient Absence Duration

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C0030705
UMLS CUI [1,3]
C0332197
UMLS CUI [1,4]
C0449238
previous therapy for known breast cancer.
Beschreibung

Prior Therapy Breast Carcinoma

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0678222
those who have had tram (i.e., transabdominal rectus abdominus muscle reconstructive surgery) done.
Beschreibung

Breast reconstruction with TRAM flap

Datentyp

boolean

Alias
UMLS CUI [1]
C1960508
moderate lymphedema (>20% or >200ml difference between the affected arm and the unaffected arm).
Beschreibung

Lymphedema Moderate

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0024236
UMLS CUI [1,2]
C0205081
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Breast Neoplasms NCT00115713

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Early-Stage Breast Carcinoma | TNM clinical staging
Item
breast cancer early stage i –iiia
boolean
C2986665 (UMLS CUI [1])
C3258246 (UMLS CUI [2])
Operative Surgical Procedure Axillary Completed
Item
completed axillary surgery
boolean
C0543467 (UMLS CUI [1,1])
C0004454 (UMLS CUI [1,2])
C0205197 (UMLS CUI [1,3])
Adjuvant Chemotherapy Planned
Item
scheduled to receive adjuvant chemotherapy for 9 – 24 weeks
boolean
C0085533 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Approval Oncologist Treating
Item
approval of the treating oncologist
boolean
C0205540 (UMLS CUI [1,1])
C0259990 (UMLS CUI [1,2])
C1522326 (UMLS CUI [1,3])
Comprehension English Language | Comprehension French language | Informed Consent English Language | Informed Consent French language
Item
able to understand and provide written informed consent in english or french (ottawa)
boolean
C0162340 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C0376246 (UMLS CUI [2,2])
C0021430 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
C0021430 (UMLS CUI [4,1])
C0376246 (UMLS CUI [4,2])
Age
Item
18+ years of age
boolean
C0001779 (UMLS CUI [1])
Uncontrolled hypertension | Heart Diseases | Mental disorders
Item
no uncontrolled hypertension, cardiac illness, psychiatric condition
boolean
C1868885 (UMLS CUI [1])
C0018799 (UMLS CUI [2])
C0004936 (UMLS CUI [3])
Medical contraindication Exercise | Fitness Test
Item
no contraindication to exercise as determined by a fitness test
boolean
C1301624 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
C0031812 (UMLS CUI [2,1])
C0456984 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnant.
boolean
C0032961 (UMLS CUI [1])
Randomization Unwilling
Item
unwilling to accept randomization.
boolean
C0034656 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
medical condition Contraindication Exercise
Item
any medical condition that would be a contraindication to exercise. the clinicians will make this decision.
boolean
C3843040 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
Exercise Program participation Unwilling
Item
unwilling to travel to/participate in the exercise program as defined by the protocol.
boolean
C0015259 (UMLS CUI [1,1])
C3484370 (UMLS CUI [1,2])
C0679823 (UMLS CUI [1,3])
C0558080 (UMLS CUI [1,4])
Prior Chemotherapy | Malignant Neoplasms
Item
previous chemotherapy (previous cancer is not an exclusion criteria).
boolean
C1514457 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
cancer recurrence
Item
cancer recurrence.
boolean
C0920420 (UMLS CUI [1])
Clinical Trial Patient Absence Duration
Item
planned/known absence of greater than 2 weeks during the intended study period.
boolean
C0008976 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0449238 (UMLS CUI [1,4])
Prior Therapy Breast Carcinoma
Item
previous therapy for known breast cancer.
boolean
C1514463 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Breast reconstruction with TRAM flap
Item
those who have had tram (i.e., transabdominal rectus abdominus muscle reconstructive surgery) done.
boolean
C1960508 (UMLS CUI [1])
Lymphedema Moderate
Item
moderate lymphedema (>20% or >200ml difference between the affected arm and the unaffected arm).
boolean
C0024236 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
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