ID

38217

Descripción

Moving Forward: A Weight Loss Intervention for African-American Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT02482506

Link

https://clinicaltrials.gov/show/NCT02482506

Palabras clave

Versiones (1)
  1. 28/9/19 28/9/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 de septiembre de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT02482506

Inglés

Eligibility Breast Cancer NCT02482506

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
self-identification as black or african american (including individuals who are bi-racial but identify themselves as black or aa)
Descripción

Black | African American

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005680
UMLS CUI [2]
C0085756
female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
stage i, ii, and iii invasive breast carcinoma
Descripción

Invasive carcinoma of breast TNM Breast tumor staging

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0853879
UMLS CUI [1,2]
C0474926
treatment (surgery, chemotherapy and/or radiation) completed at least 6 months prior to recruitment (ongoing treatment with tamoxifen or ais is acceptable)
Descripción

Treatment completed | Operative Surgical Procedures | Chemotherapy | Therapeutic radiology procedure | Tamoxifen Continuous | Aromatase Inhibitors Continuous |

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0580352
UMLS CUI [2]
C0543467
UMLS CUI [3]
C0392920
UMLS CUI [4]
C1522449
UMLS CUI [5,1]
C0039286
UMLS CUI [5,2]
C0549178
UMLS CUI [6,1]
C0593802
UMLS CUI [6,2]
C0549178
age 18 or above at time of diagnosis
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
bmi at least 25 km/m2
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
physically able to participate in a moderate physical activity program as assessed by a screening questionnaire and pcp approval.
Descripción

Participation Moderate physical activity Program | Assessment Screening questionnaire

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C4482418
UMLS CUI [1,3]
C3484370
UMLS CUI [2,1]
C1516048
UMLS CUI [2,2]
C1134635
agreeable to random assignment and data collection including blood draw.
Descripción

Random assignment | Data Collection | Blood draw

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0814868
UMLS CUI [2]
C0010995
UMLS CUI [3]
C0005834
able to attend twic weekly classes for 6 months.
Descripción

Other Coding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3846158
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
plans to move from the community during the study
Descripción

Relocation of home Planned

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
medical condition limiting adherence as assessed by pcp
Descripción

Medical condition Limiting Adherence

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C1510802
history of significant mental illness
Descripción

Mental disorder

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0004936
currently pregnant, less than 3 months post-partum, or pregnancy anticipated during the study..
Descripción

Pregnancy | Postpartum Period | Pregnancy, Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0086839
UMLS CUI [3]
C0032992
current/planned use of an fda-approved or over the counter weight loss medication.
Descripción

Weight-Loss Agents | Non-Prescription Weight-Loss Agents

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376606
UMLS CUI [2,1]
C0013231
UMLS CUI [2,2]
C0376606
participation in another structured weight loss program
Descripción

Participation Weight Reduction Program

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C3179079
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Similar models

Eligibility Breast Cancer NCT02482506

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Black | African American
Item
self-identification as black or african american (including individuals who are bi-racial but identify themselves as black or aa)
boolean
C0005680 (UMLS CUI [1])
C0085756 (UMLS CUI [2])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Invasive carcinoma of breast TNM Breast tumor staging
Item
stage i, ii, and iii invasive breast carcinoma
boolean
C0853879 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Treatment completed | Operative Surgical Procedures | Chemotherapy | Therapeutic radiology procedure | Tamoxifen Continuous | Aromatase Inhibitors Continuous |
Item
treatment (surgery, chemotherapy and/or radiation) completed at least 6 months prior to recruitment (ongoing treatment with tamoxifen or ais is acceptable)
boolean
C0580352 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0392920 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
C0039286 (UMLS CUI [5,1])
C0549178 (UMLS CUI [5,2])
C0593802 (UMLS CUI [6,1])
C0549178 (UMLS CUI [6,2])
Age
Item
age 18 or above at time of diagnosis
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
bmi at least 25 km/m2
boolean
C1305855 (UMLS CUI [1])
Participation Moderate physical activity Program | Assessment Screening questionnaire
Item
physically able to participate in a moderate physical activity program as assessed by a screening questionnaire and pcp approval.
boolean
C0679823 (UMLS CUI [1,1])
C4482418 (UMLS CUI [1,2])
C3484370 (UMLS CUI [1,3])
C1516048 (UMLS CUI [2,1])
C1134635 (UMLS CUI [2,2])
Random assignment | Data Collection | Blood draw
Item
agreeable to random assignment and data collection including blood draw.
boolean
C0814868 (UMLS CUI [1])
C0010995 (UMLS CUI [2])
C0005834 (UMLS CUI [3])
Other Coding
Item
able to attend twic weekly classes for 6 months.
boolean
C3846158 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Relocation of home Planned
Item
plans to move from the community during the study
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Medical condition Limiting Adherence
Item
medical condition limiting adherence as assessed by pcp
boolean
C3843040 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1510802 (UMLS CUI [1,3])
Mental disorder
Item
history of significant mental illness
boolean
C0004936 (UMLS CUI [1])
Pregnancy | Postpartum Period | Pregnancy, Planned
Item
currently pregnant, less than 3 months post-partum, or pregnancy anticipated during the study..
boolean
C0032961 (UMLS CUI [1])
C0086839 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Weight-Loss Agents | Non-Prescription Weight-Loss Agents
Item
current/planned use of an fda-approved or over the counter weight loss medication.
boolean
C0376606 (UMLS CUI [1])
C0013231 (UMLS CUI [2,1])
C0376606 (UMLS CUI [2,2])
Participation Weight Reduction Program
Item
participation in another structured weight loss program
boolean
C0679823 (UMLS CUI [1,1])
C3179079 (UMLS CUI [1,2])
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