ID

38122

Descrição

Adapted Physical Activity Effect on Aerobic Function and Fatigue at Home in Patients With Breast Cancer Treated in Adjuvant or Neoadjuvant Phase; ODM derived from: https://clinicaltrials.gov/show/NCT01795612

Link

https://clinicaltrials.gov/show/NCT01795612

Palavras-chave

Versões (1)
  1. 19/09/2019 19/09/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

19 de setembro de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Breast Cancer NCT01795612

Inglês

Eligibility Breast Cancer NCT01795612

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
females between 18 and 75 years of age;
Descrição

Gender | Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
signed written informed consent;
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
willing to take part in the trial and to follow the instructions;
Descrição

Study Subject Participation Status Willing | Adherence Instructions

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0600109
UMLS CUI [2,1]
C1510802
UMLS CUI [2,2]
C1442085
breast tumour, histologically documented;
Descrição

Breast Carcinoma

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0678222
patients for whom a 6-treatment course of adjuvant or neoadjuvant chemotherapy (3fec100 +3 taxanes or 6 fec) +/- radiotherapy+/- herceptin has been scheduled;
Descrição

Scheduled treatment | Adjuvant Chemotherapy Quantity | Neoadjuvant Chemotherapy Quantity | FEC | Taxanes | Therapeutic radiology procedure | Therapeutic radiology procedure Absent | Herceptin | Herceptin Absent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3844437
UMLS CUI [2,1]
C0085533
UMLS CUI [2,2]
C1265611
UMLS CUI [3,1]
C0600558
UMLS CUI [3,2]
C3665472
UMLS CUI [3,3]
C1265611
UMLS CUI [4]
C0060133
UMLS CUI [5]
C0796419
UMLS CUI [6]
C1522449
UMLS CUI [7,1]
C1522449
UMLS CUI [7,2]
C0332197
UMLS CUI [8]
C0338204
UMLS CUI [9,1]
C0338204
UMLS CUI [9,2]
C0332197
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic cancer;
Descrição

Neoplasm Metastasis

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0027627
disability preventing a proper understanding of the instructions for the trial;
Descrição

Disability Preventing Comprehension Instructions

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0231170
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C0162340
UMLS CUI [1,4]
C1442085
patients who are subject to a court protection, wardship or guardianship order;
Descrição

Court of protection certificate status | Patients Wardship | Patients Guardianship

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0585789
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C0556263
UMLS CUI [3,1]
C0030705
UMLS CUI [3,2]
C0870627
uncontrolled hypertension;
Descrição

Uncontrolled hypertension

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1868885
family history of sudden death in a first-degree relative;
Descrição

Family history of sudden death First Degree Relative

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2315244
UMLS CUI [1,2]
C1517194
unstabilised heart disease;
Descrição

Heart Disease Unstable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0443343
current treatment with beta-blockers;
Descrição

Adrenergic beta-1 Receptor Antagonists

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0304516
chronic or acute pulmonary disease associated with dyspnoea upon moderate effort;
Descrição

Chronic lung disease | Lung disease Associated with Dyspnea on exertion | Dyspnea Effort Moderate

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0746102
UMLS CUI [2,1]
C0024115
UMLS CUI [2,2]
C0332281
UMLS CUI [2,3]
C0231807
UMLS CUI [3,1]
C0013404
UMLS CUI [3,2]
C0015264
UMLS CUI [3,3]
C0205081
uncontrolled thyroid dysfunction;
Descrição

Thyroid dysfunction Uncontrolled

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0348024
UMLS CUI [1,2]
C0205318
uncontrolled diabetes;
Descrição

Diabetic - poor control

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0421258
any other serious conditions that are unstabilised,
Descrição

Condition Serious Unstable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0443343
disabling or in which physical exercise is contra-indicated;
Descrição

Disabling condition | Physical exercise Contraindicated

Tipo de dados

boolean

Alias
UMLS CUI [1]
C4061999
UMLS CUI [2,1]
C0015259
UMLS CUI [2,2]
C1444657
unable to attend for follow-up throughout the duration of the study;
Descrição

Follow-up Attend Unable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1999232
UMLS CUI [1,3]
C1299582
ventricular ejection fraction (vef) < 50%, pregnancy or suckling.
Descrição

Ventricular Ejection Fraction | Pregnancy | Breast Feeding

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0042508
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0006147
Voltar ao início da página

Similar models

Eligibility Breast Cancer NCT01795612

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Age
Item
females between 18 and 75 years of age;
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Informed Consent
Item
signed written informed consent;
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status Willing | Adherence Instructions
Item
willing to take part in the trial and to follow the instructions;
boolean
C2348568 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C1510802 (UMLS CUI [2,1])
C1442085 (UMLS CUI [2,2])
Breast Carcinoma
Item
breast tumour, histologically documented;
boolean
C0678222 (UMLS CUI [1])
Scheduled treatment | Adjuvant Chemotherapy Quantity | Neoadjuvant Chemotherapy Quantity | FEC | Taxanes | Therapeutic radiology procedure | Therapeutic radiology procedure Absent | Herceptin | Herceptin Absent
Item
patients for whom a 6-treatment course of adjuvant or neoadjuvant chemotherapy (3fec100 +3 taxanes or 6 fec) +/- radiotherapy+/- herceptin has been scheduled;
boolean
C3844437 (UMLS CUI [1])
C0085533 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0600558 (UMLS CUI [3,1])
C3665472 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0060133 (UMLS CUI [4])
C0796419 (UMLS CUI [5])
C1522449 (UMLS CUI [6])
C1522449 (UMLS CUI [7,1])
C0332197 (UMLS CUI [7,2])
C0338204 (UMLS CUI [8])
C0338204 (UMLS CUI [9,1])
C0332197 (UMLS CUI [9,2])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis
Item
metastatic cancer;
boolean
C0027627 (UMLS CUI [1])
Disability Preventing Comprehension Instructions
Item
disability preventing a proper understanding of the instructions for the trial;
boolean
C0231170 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C0162340 (UMLS CUI [1,3])
C1442085 (UMLS CUI [1,4])
Court of protection certificate status | Patients Wardship | Patients Guardianship
Item
patients who are subject to a court protection, wardship or guardianship order;
boolean
C0585789 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C0556263 (UMLS CUI [2,2])
C0030705 (UMLS CUI [3,1])
C0870627 (UMLS CUI [3,2])
Uncontrolled hypertension
Item
uncontrolled hypertension;
boolean
C1868885 (UMLS CUI [1])
Family history of sudden death First Degree Relative
Item
family history of sudden death in a first-degree relative;
boolean
C2315244 (UMLS CUI [1,1])
C1517194 (UMLS CUI [1,2])
Heart Disease Unstable
Item
unstabilised heart disease;
boolean
C0018799 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
Adrenergic beta-1 Receptor Antagonists
Item
current treatment with beta-blockers;
boolean
C0304516 (UMLS CUI [1])
Chronic lung disease | Lung disease Associated with Dyspnea on exertion | Dyspnea Effort Moderate
Item
chronic or acute pulmonary disease associated with dyspnoea upon moderate effort;
boolean
C0746102 (UMLS CUI [1])
C0024115 (UMLS CUI [2,1])
C0332281 (UMLS CUI [2,2])
C0231807 (UMLS CUI [2,3])
C0013404 (UMLS CUI [3,1])
C0015264 (UMLS CUI [3,2])
C0205081 (UMLS CUI [3,3])
Thyroid dysfunction Uncontrolled
Item
uncontrolled thyroid dysfunction;
boolean
C0348024 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
Diabetic - poor control
Item
uncontrolled diabetes;
boolean
C0421258 (UMLS CUI [1])
Condition Serious Unstable
Item
any other serious conditions that are unstabilised,
boolean
C0348080 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0443343 (UMLS CUI [1,3])
Disabling condition | Physical exercise Contraindicated
Item
disabling or in which physical exercise is contra-indicated;
boolean
C4061999 (UMLS CUI [1])
C0015259 (UMLS CUI [2,1])
C1444657 (UMLS CUI [2,2])
Follow-up Attend Unable
Item
unable to attend for follow-up throughout the duration of the study;
boolean
C3274571 (UMLS CUI [1,1])
C1999232 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
Ventricular Ejection Fraction | Pregnancy | Breast Feeding
Item
ventricular ejection fraction (vef) < 50%, pregnancy or suckling.
boolean
C0042508 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Voltar ao início da página 

Contacto

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial