ID

42620

Descripción

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

Palabras clave

Versiones (2)
  1. 17/7/16 17/7/16 -
  2. 17/9/21 17/9/21 -
Subido en

17 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Neoplasms NCT00115713

Inglés

Eligibility Breast Neoplasms NCT00115713

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

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

Early-Stage Breast Carcinoma | TNM clinical staging

Tipo de datos

boolean

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

Operative Surgical Procedure Axillary Completed

Tipo de datos

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
Descripción

Adjuvant Chemotherapy Planned

Tipo de datos

boolean

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

Approval Oncologist Treating

Tipo de datos

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)
Descripción

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

Tipo de datos

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
Descripción

Age

Tipo de datos

boolean

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

Uncontrolled hypertension | Heart Diseases | Mental disorders

Tipo de datos

boolean

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

Medical contraindication Exercise | Fitness Test

Tipo de datos

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant.
Descripción

Pregnancy

Tipo de datos

boolean

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

Randomization Unwilling

Tipo de datos

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.
Descripción

medical condition Contraindication Exercise

Tipo de datos

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.
Descripción

Exercise Program participation Unwilling

Tipo de datos

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).
Descripción

Prior Chemotherapy | Malignant Neoplasms

Tipo de datos

boolean

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

cancer recurrence

Tipo de datos

boolean

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

Clinical Trial Patient Absence Duration

Tipo de datos

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.
Descripción

Prior Therapy Breast Carcinoma

Tipo de datos

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.
Descripción

Breast reconstruction with TRAM flap

Tipo de datos

boolean

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

Lymphedema Moderate

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0024236
UMLS CUI [1,2]
C0205081
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Similar models

Eligibility Breast Neoplasms NCT00115713

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
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